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Aliases & Descriptions for JUN gene
(According to
1 HGNC ,
2 Entrez Gene ,
3 UniProtKB/Swiss-Prot ,
4 UniProtKB/TrEMBL , 5 OMIM , 6 GeneLoc
, and/or 7 Ensembl ,
8 miRBase )About This Section
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User Feedback Aliases & Descriptions jun oncogene1 2 p392 3 V-jun avian sarcoma virus 17 oncogene homolog1 2 3 v-jun sarcoma virus 17 oncogene homolog (avian)1 AP-11 2 Jun activation domain binding protein2 c-Jun1 2 transcription factor AP-12 Proto-oncogene c-Jun2 3 enhancer-binding protein AP12 Activator protein 12 3 v-jun sarcoma virus 17 oncogene homolog2 AP12 3
Search outside databases for aliases for JUN genePrevious GC identifers: GC01M058161 GC01M058604 GC01M058616 GC01M058958
Summaries for JUN gene (According to Entrez Gene ,
Tocris Bioscience ,
Wikipedia's
Gene Wiki ,
UniProtKB/Swiss-Prot ,
and/or
UniProtKB/TrEMBL )
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User Feedback Entrez Gene summary for JUN : This gene is the putative transforming gene of avian sarcoma virus 17. It encodes a protein which is highly similar to the viral protein, and which interacts directly with specific target DNA sequences to regulate gene expression. This gene is intronless and is mapped to 1p32-p31, a chromosomal region involved in both translocations and deletions in human malignancies. (provided by RefSeq) UniProtKB/Swiss-Prot: JUN_HUMAN, P05412 Function : Transcription factor that recognizes and binds to the enhancer heptamer motif 5'-TGA[CG]TCA-3'Gene Wiki entry for JUN (C-jun)
Genomic Views for JUN gene
(According to
GeneLoc and/or
HGNC , and/or
Entrez Gene (NCBI build 37) ,
and/or miRBase ,
Genomic Views according to
UCSC and
Ensembl (release 56) ,
Regulatory elements and Epigenetics data according to
SABiosciences )About This Section
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User Feedback Regulatory elements: SABiosciences Regulatory transcription factor binding sites in the JUN gene upstream (promoter) region :NF-kappaB1 NF-kappaB PPAR-gamma2 PPAR-gamma1 GCNF-1 GCNF-2 MEF-2A deltaCREB CREB GATA-3 Epigenetics: SABiosciences Methyl-Profiler DNA Methylation qPCR Primer Assays for JUN: MePH01101-2A Genomic Location: Genomic View : UCSC Golden Path with GeneCards custom track Entrez Gene cytogenetic band: 1p32-p31 Ensembl cytogenetic band: 1p32.1 HGNC cytogenetic band: 1p32-p31 JUN Gene in genomic location: bands according to Ensembl, locations according to
(and/or Entrez Gene and/or Ensembl if different) GeneLoc gene densities for chromosome 1 GeneLoc Exon Structure
GeneLoc location for GC01M059163: view genomic region
(about GC identifiers )
Start:
59,246,463 bp from pter
End:
59,249,785 bp from pter
Size:
3,323 bases
Orientation:
minus strand
RefSeq DNA sequence: NC_000001.10 NT_032977.9 Proteins for JUN gene
(According to
1 UniProtKB ,
and/or Ensembl ,
Phosphorylation sites according to 2 Phosphosite ,
RefSeq according to NCBI ,
PDB rendering according to OCA and/or Proteopedia ,
Recombinant Proteins
from
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Enzo Life Sciences ,
Abnova ,
OriGene ,
Novus Biologicals , and/or
Sino Biological ,
Biochemical Assays by
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Cell Signaling Technology , and/or
Enzo Life Sciences ,
Ontologies according to Gene
Ontology Consortium 01 May 2010 and
Entrez Gene ,
Antibodies by
Millipore ,
Sigma-Aldrich ,
R&D Systems ,
Cell Signaling Technology ,
Abnova ,
OriGene ,
Novus Biologicals , and/or
Epitomics )
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User Feedback UniProtKB/Swiss-Prot: JUN_HUMAN, P05412 (See
protein sequence )Recommended Name: Transcription factor AP-1 Size : 331 amino acids; 35676 Da
Subunit : Heterodimer with either FOS or BATF3. Interacts with HIVEP3 (By similarity). Interacts with SMAD3/SMAD4heterodimers. Interacts with MYBBP1A, SP1, SPIB and TCF20. Interacts with COPS5; indirectly leading to its phosphorylation. Interacts with DSIPI; this interaction inhibits the binding of active AP1 to its target DNA
Subcellular location : Nucleus
PDB structures from and Proteopedia : 1A02 (3D)
 1FOS (3D)
 1JNM (3D)
 1JUN (3D)
 1S9K (3D)
 1T2K (3D)
 
Secondary accessions : Q96G93Post-translational modifications:
Phosphorylation enhances the transcriptional activity. Phosphorylated by PRKDC1
View phosphorylation sites using PhosphoSite 2
REFSEQ proteins: NP_002219.1 ENSEMBL proteins: ENSP00000360266 Human Recombinant Proteins 5 Gene Ontology (GO) cellular component terms (GO ID links to tree view) :
About this table
JUN for ontologies About GeneDecksing Antibodies for JUN: Millipore Mono- and Polyclonal Antibodies for the study of JUN Sigma-Aldrich Antibody Arrays and Antibodies for JUN R&D Systems Antibodies for JUN (c-Jun) Cell Signaling Technology (CST) Antibodies for JUN (JUN , c-Jun ) Monoclonal and Polyclonal Antibodies from Abnova (JUN ) Origene Antibodies (see all 13 ): JUN Novus Biologicals Antibodies for JUN Epitomics antibodies for JUN
Assays for JUN:
Protein
Domains/ Families for JUN gene(According to InterPro , ProtoNet ,
UniProtKB , and/or BLOCKS ,
Sets of similar genes according to GeneDecks )
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JUN for domains About GeneDecksing 5/6 InterPro domains/families (see all 6
):
Graphical View of Domain Structure for InterPro Entry P05412 ProtoNet protein and cluster: P05412
3 Blocks protein families : IPB002112 Jun transcription factor signature IPB005643 Jun-like transcription factor IPB011616 bZIP transcription factor UniProtKB/Swiss-Prot: JUN_HUMAN, P05412 Similarity : Belongs to the bZIP family. Jun subfamilySimilarity : Contains 1 bZIP domain
Gene Function for JUN gene
(According to MGI May 08 2010, UniProtKB ,
IUBMB ,and/or Genatlas ,
shRNA from
OriGene ,
Sigma-Aldrich , RNAi from
Millipore ,
Abnova ,
siRNAs from
Applied Biosystems ,
Sigma-Aldrich , Clones from
Millipore ,
Sigma-Aldrich ,
OriGene ,
Sino Biological ,
Ontologies according to Gene Ontology Consortium 01 May 2010 via
Entrez Gene .)
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User Feedback UniProtKB/Swiss-Prot: JUN_HUMAN, P05412 Function : Transcription factor that recognizes and binds to the enhancer heptamer motif 5'-TGA[CG]TCA-3'
Genatlas biochemistry entry for JUN :avian sarcoma virus 17 (v-jun) oncogene homolog,ligand induced,immediate (primary ) early response gene interacting with MYC to regulate AP1 genes 5/12 Gene Ontology (GO) molecular function terms (GO ID links to tree view) (see all 12
):
About this table
JUN for ontologies About GeneDecksing Animal Models: 15/18 MGI mutant phenotypes (inferred from 10 alleles ) (MGI details for Jun) (see all 18
):
JUN for phenotypes About GeneDecksing Pathways & Interactions for JUN gene
(Pathways according to
Millipore ,
Cell Signaling Technology ,
Sigma-Aldrich ,
Applied Biosystems GeneAssist ,
KEGG
and/or UniProtKB ,
(map by GeneGo ),
Sets of similar genes according to GeneDecks ,
Proteins Network according to
SABiosciences ,
Interactions according to 1 UniProtKB ,
2 MINT , and/or
3 STRING ,
with links to IntAct and
Ensembl ,
Ontologies according to Gene Ontology Consortium 01 May 2010 via
Entrez Gene) .
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JUN for pathways About GeneDecksing 5/51 Millipore Pathways for JUN (see all 51
)5/75 Sigma-Aldrich "Your Favorite Gene" Pathways for JUN (Your Favorite Gene powered by Ingenuity) (see all 75
)5/99 GeneAssist Pathways for JUN (see all 99
)3
Cell Signaling Technology (CST) Pathways for JUN:
5/14 Kegg Pathways (Kegg details for JUN) (see all 14
): SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for JUN 5/20 Interacting proteins for JUN (P05412 1 , 2 ) via UniProtKB, MINT, and/or STRING (see all 20
) About this table 5/30 Gene Ontology (GO) biological process terms (GO ID links to tree view) (see all 30
):
GO ID Qualified GO term Evidence PubMed IDs GO:0001525 angiogenesis
IEA -- GO:0001836 release of cytochrome c from mitochondria
IEA -- GO:0006355 regulation of transcription, DNA-dependent
IEA -- GO:0007179 transforming growth factor beta receptor signaling pathway
IDA 9732876 GO:0007184 SMAD protein nuclear translocation
IDA 9732876
About this table
JUN for ontologies About GeneDecksing
Drugs & Compounds for JUN gene (Chemical Compounds according to UniProtKB , Enzo Life Sciences ,
Sigma-Aldrich , Tocris Bioscience , and/or
Novoseek and Drugs according to
Enzo Life Sciences and/or
PharmGKB )
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JUN for compounds About GeneDecksing
Enzo Life Sciences drugs & compounds for JUN
Browse Tocris compounds for JUN 10/1361 Novoseek chemical compound relationships for JUN gene (see all 1361
)
Compound
Score
Articles
PubMed IDs for Articles with Shared Sentences (# sentences)
phorbol 12-myristate 13-acetate
100.00
724
11358830 (11), 2105946 (10), 8170999 (6), 1939341 (6) (see all 100 )
sp600125
100.00
155
12031798 (4), 19405983 (2), 18487435 (2), 18251700 (2) (see all 100 )
curcumin
100.00
227
16157375 (6), 16053715 (5), 9439980 (4), 7955078 (4) (see all 100 )
phorbol
54.98
85
1901643 (3), 1850629 (3), 9037208 (2), 8892460 (2) (see all 74 )
leucine
50.60
264
2509385 (5), 15087451 (5), 8112339 (4), 2501150 (4) (see all 100 )
pd 98059
49.79
102
15627897 (2), 15240007 (2), 12592382 (2), 12016209 (2) (see all 96 )
okadaic acid
44.32
114
9022811 (8), 1851743 (8), 1419903 (6), 12036911 (6) (see all 53 )
sb203580
28.89
62
15240007 (2), 11367542 (2), 11053056 (2), 9973495 (1) (see all 59 )
retinoic acid
22.30
326
9377582 (8), 12494454 (7), 10329043 (7), 9139741 (6) (see all 100 )
15-deoxy-delta-12,14-prostaglandin j2
18.68
41
14532268 (7), 15289320 (4), 14693716 (3), 12774315 (3) (see all 23 )
About this table 2 PharmGKB drug compound relationships for JUN gene About this table
Transcripts for JUN gene(GenBank/EMBL/DDBJ Accessions according to
Unigene
(Build 223 Homo sapiens; Apr 2 2010) or GenBank , RefSeq according to Entrez Gene ,
DOTS (version 10), and/or
AceView ,
non coding RNAs according to
RNAdb ,
ESTs according to GeneTide ,
exon structure from GeneLoc ,
alternative splicing isoforms according to ASD and/or
ECgene ,
RNAi Products from
Millipore and/or
Abnova ,
siRNAs from Applied Biosystems ,
Sigma-Aldrich ,
shRNA from
Sigma-Aldrich ,
OriGene ,
microRNA from SABiosciences ,
Tagged/untagged cDNA clones from
OriGene ,
Primers from
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SABiosciences , Expression Assays from Applied Biosystems )About This Section
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User Feedback Assays: Applied Biosystems TaqMan® Gene Expression Assays: NM_002228 Clones: Origene GFP tagged cDNA clones in CMV expression vector: JUN Origene Myc/DDK tagged cDNA clones in CMV expression vector: JUN Origene untagged cDNA clones in CMV expression vector: JUN
Primers: Origene genome-wide validated SYBR primer pairs: JUN SABiosciences RT2 qPCR Primer Assay for JUN: PPH00095A
REFSEQ mRNAs for JUN gene: NM_002228.3
Additional cDNA sequence: AK307137.1 BC002646.2 BC006175.1 BC009874.2 BC068522.1 BT019759.1 CR541724.1 CR541752.1
22 DOTS entries : DT.97762702 DT.100044313 DT.121359986 DT.121359920 DT.450792 DT.100675414 DT.100863059 DT.100675418
DT.100851939 DT.121359919 DT.121359948 DT.92473418 DT.95264854 DT.95107720 DT.121359935 DT.95132043 DT.100804761 DT.91897383 DT.92473595 DT.100675423 DT.121359950 DT.91843574 24/886 AceView cDNA sequences (see all 886
):
CA952681 BU617685 CA395719 AW071971 AW007689 BM747239 BE890895 AA476238 AI077423 BQ269083 AA029968 BM750603 AA992452 AI262566 N70643 H45005 AI340023 BM767296 AI697220 BQ186100 BM767396 BM127784 CB155645 CA865626
highest scoring ESTs for JUN :AW005304 AA027941 AA040560 AA159143 AA179925 AA281805 AA351935 AA362757 AA423803 AA436799 Unigene Cluster for JUN:
Jun oncogene Hs.723911 [show with all ESTs ] Unigene Representative Sequence: NM_002228 GeneLoc Exon Structure 1 Ensembl transcript including schematic representation : ENST00000371222
Expression for JUN gene
(Experimental results according to
1 GeneNote
and GNF BioGPS ,
probe sets-to-genes annotations according to
2 GeneAnnot ,
3 GeneTide ,
Sets of similar genes according to GeneDecks ,
Electronic Northern calculations according to data from
UniGene (Build 223 Homo sapiens),
SAGE tags according to
CGAP ,
plus additional links to
SOURCE , and/or
GNF
BioGPS , and/or
EXPOLDB , and/or
UniProtKB ,
Expression Assays from
Applied Biosystems ,
Primers from
OriGene and/or
SABiosciences
)
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User Feedback JUN expression in normal and diseased human tissues Applied Biosystems TaqMan ® Gene Expression Assays for JUN 1 / 2 / 3
9 probe-sets matching JUN gene
Affymetrix probe-set
Array
GeneAnnot data
GeneNote data
GeneTide data
# genes
Sensitivity
Specificity
Correlation
Length
Gb_Accession
Consensus
Uniqueness
Score
Rank
89913_s_at2 , 3
U95-D
1
0.75
1.00
0.95
1.10
AW005304
1.00
1.00
1.00
1
32583_at*2 , 3
U95-A
1
--
--
0.96
1.03
J04111
0.20
1.00
0.72
1
1895_at*2 , 3
U95-A
1
--
--
0.94
0.87
J04111
0.20
1.00
0.72
1
201465_s_at2 , 3
U133-A
1
0.82
1.00
--
--
BC002646
0.80
1.00
0.91
1
201466_s_at2 , 3
U133-A
1
0.36
1.00
--
--
NM_002228
0.60
1.00
0.82
1
201464_x_at2 , 3
U133-A
1
0.27
1.00
--
--
BG491844
0.40
1.00
0.76
1
201465_s_at2
U133Plus2
1
0.82
1.00
--
--
--
--
--
--
--
201466_s_at2
U133Plus2
1
0.36
1.00
--
--
--
--
--
--
--
201464_x_at2
U133Plus2
1
0.27
1.00
--
--
--
--
--
--
--
About this table
JUN for expression About GeneDecksing Data from
Genenote  
(Publications) and GNF BioGPS About these images About these images CGAP SAGE TAG: CCTTTGTAAG SOURCE GeneReport for Unigene cluster: Hs.723911 Expression variation in blood from EXPOLDB for JUN
Primers: Origene genome-wide validated SYBR primer pairs: JUN SABiosciences RT2 qPCR Primer Assay for JUN: PPH00095A
Orthologs for JUN gene
(Orthologs according to
1,2 HomoloGene (2 older version, for species not in 1 newer version),
3 euGenes ,
4 SGD
and/or
5 MGI May 08 2010,
with possible further links to
Flybase
and/or
WormBase ,
Gene Trees according to Ensembl )
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Orthologs for JUN gene from 5/9 species (see all 9
)
About this table Species with no ortholog for JUN ENSEMBL Gene Tree for JUN Paralogs for JUN gene (Paralogs according to 1 HomoloGene and 2 Ensembl , Pseudogenes according to 3 Pseudogene.org )About This Section
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User Feedback Paralogs for JUN gene JUND 2 JUNB 2
JUN for paralogs About GeneDecksing
Genomic Variants for JUN gene (SNPs according to the
1 NCBI SNP Database ,
2 Ensembl ,
3 PupaSUITE , and
UniProtKB ,
Linkage Disequilibrium by HapMap ,
Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants ,
Genotyping Reagents from
Applied Biosystems )
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HapMap Linkage Disequilibrium images for JUN (up to first 250kb)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions) Database of Genomic Variants (DGV): 1 variation for JUN 1 CNV : 63848
Disorders & Mutations for JUN gene
(in which this Gene is Involved, According to
OMIM, UniProtKB ,
Novoseek , PharmGKB ,
Genatlas , GeneTests ,
Blood group antigen gene mutations by BGMUT ,
LSDB, HGMD, GAD ,
HuGE Navigator ,
BCGD,
and/or TGDB .)
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JUN for disorders About GeneDecksing
OMIM: 165160 10/757 Novoseek disease relationships for JUN gene (see all 757
)
Disease
Score
Articles
PubMed IDs for Articles with Shared Sentences (# sentences)
dominant-negative mutant
84.83
92
8853897 (3), 8108121 (3), 8455942 (2), 19405983 (2) (see all 81 )
cell transformation
71.77
133
11416221 (5), 8189491 (4), 15886210 (4), 1516834 (4) (see all 90 )
tumor promotion
28.74
52
8631126 (2), 15064752 (2), 12036911 (2), 9472093 (1) (see all 49 )
neoplastic transformation
14.06
45
18757399 (2), 1801783 (2), 1773784 (2), 1543542 (2) (see all 38 )
skin carcinogenesis
10.79
23
9485025 (2), 12616721 (2), 20179211 (1), 19057013 (1) (see all 21 )
oncogenesis
9.23
40
11402340 (3), 1516834 (2), 9819389 (1), 9228025 (1) (see all 37 )
nuclear accumulation
8.14
28
14572605 (2), 11358991 (2), 8344964 (1), 20028981 (1) (see all 26 )
junin
5.66
13
16817762 (6), 1681712 (5), 8623541 (2)
glucocorticoid resistance
5.39
9
10500841 (4), 16164226 (3), 11237062 (2)
leukemia myeloid
5.13
34
2122980 (3), 8622627 (2), 8058058 (2), 2174893 (2) (see all 23 )
About this table 1 PharmGKB disease relationship for JUN gene About this table Human Genome Epidemiology Navigator: JUN (114 documents) Tumor Gene Database : JUN
Medical News for JUN gene (Possibly Related Articles in
Doctor's Guide )
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Publications for JUN gene (in
PubMed .
Associations of this gene to articles via
1 Novoseek ,
2 HGNC ,
3 Entrez Gene ,
4 UniProtKB/Swiss-Prot ,
5 UniProtKB/TrEMBL ,
6 GAD , and/or
7 PharmGKB )
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User Feedback 10/5762 PubMed articles for JUN gene (see all 5762
): Structure and chromosomal localization of the functional intronless human JUN protooncogene. (PubMed id 3194415) 2, 3 , 4 Hattori K.... Karin M. (1988) A new group of conserved coactivators that increase the specificity of AP-1 transcription factors. (PubMed id 8837781) 1, 3 , 4 Claret F.-X.... Karin M. (1996) High resolution NMR solution structure of the leucine zipper domain of the c-Jun homodimer. (PubMed id 8662824) 1, 3 , 4 Junius F.K.... King G.F. (1996) Cross-talk between different enhancer elements during mitogenic induction of the human stromelysin-1 gene. (PubMed id 8663478) 1, 3 , 4 Kirstein M.... Saus J. (1996) c-Jun is phosphorylated by the DNA-dependent protein kinase in vitro; definition of the minimal kinase recognition motif. (PubMed id 8464713) 1, 3 , 4 Bannister A.J.... Jackson S.P. (1993) Human proto-oncogene c-jun encodes a DNA binding protein with structural and functional properties of transcription factor AP-1. (PubMed id 2825349) 1, 3 , 4 Bohmann D.... Tjian R. (1987) The DNA sequence and biological annotation of human chromosome 1. (PubMed id 16710414) 3 , 4 Gregory S.G.... Bentley D.R. (2006) Large-scale characterization of HeLa cell nuclear phosphoproteins. (PubMed id 15302935) 3 , 4 Beausoleil S.A....Gygi S.P. (2004) The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334) 3 , 4 Gerhard D.S....Malek J. (2004) Correlation of transcriptional repression by p21(SNFT) with changes in DNA.NF-AT complex interactions. (PubMed id 12087103) 3 , 4 Bower K.E....McGuire K.L. (2002)
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Aliases
JUN (Gene Symbol) jun oncogene V-jun avian sarcoma virus 17 oncogene homolog AP-1 c-Jun Proto-oncogene c-Jun Activator protein 1 AP1 p39 v-jun sarcoma virus 17 oncogene homolog (avian) Jun activation domain binding protein transcription factor AP-1 enhancer-binding protein AP1 v-jun sarcoma virus 17 oncogene homolog
Disorders
apc gene inactivation breast mouse malformation arthritis reactive lung tumor fibrosis myocardial relapse hyperthyroid h pylori infection primary effusion lymphoma epilepsies cystic fibrosis thymoma e coli infection atherosclerosis adrenal carcinoma colorectal adenocarcinoma nasal polyp endometrial cancer, stage hypoglycemia neuroblastoma human mammary carcinoma htlv-i volume overload spatial memory disorder failure heart adenoviral infection lymphoma pancreatic endocrine tumor pancreatitis osteolysis arterial thrombosis osteophyte adpkd atopic myopathies cognitive impairment diabetic complication cancer induction sclerosis; systemic abdominal aortic aneurysm arthritis, collagen-induced leukostasis metastasis degenerative adenocarcinoma endometrial necrosis globoid cell leukodystrophies acidosis primary glioblastoma glioblastoma multiforme prostate tumor chondrosarcoma psychosis cardiac; fibrosis acute leukemia epithelial tumor b-cell lymphoma osteosarcoma renal fibrosis osteoporosis spermatogenic arrest carnitine deficiency tumor initiation hepatic ischemia leukemia; myelomonocytic adenovirus infection esophageal adenocarcinoma pituitary tumor viral leukemia condyloma acuminatum ewing sarcoma chronic periodontitis benign tumor granulovacuolar degeneration traumatic neuroma leukemia plasma cell subclinical infection fibromatoses cystitis interstitial dilatations invasive breast cancer recessive dystrophic epidermolysis bullosa periodontitis escc peritonitis ovarian epithelial tumor medullary thyroid carcinoma dystrophies papilloma lupus erythematosus systemic chronic heart failure fatty liver hepatocarcinogenesis cns disease damage liver genotoxic stress immune complex; nephritis brain disease growth suppression microphthalmia fulminant hepatic failure bronchial hyperresponsiveness primary cutaneous b-cell lymphoma wallerian degeneration dependence; morphine inflammatory disease adenocarcinoma lung insulin sensitivity autoimmune disease barrett epithelium breast cancer anaplastic large cell lymphoma infarction; myocardial detachment retinal carcinoma transitional cell keratocystic odontogenic tumor tumor promotion cervical intraepithelial neoplasia chromosomal aberration neurofibrillary tangle intestinal ischemia mitochondrial alteration carcinoma; nasopharyngeal ebv infection photoreceptor degeneration skeletal neoplasm anemia; fanconi CHF enterohemorrhagic escherichia coli infection epidermodysplasia verruciformis pulmonary granulomatosis primary cutaneous marginal zone b-cell lymphoma hyperglycemia cervical cancer leukemia, t-cell novikoff hepatoma cancer other active tuberculosis prostatic adenocarcinoma abuse; drug neuroendocrine tumor CLL hepatoblastoma lichen planus breast cancer metastatic acute quadriplegic myopathy dlbcl colitis coronary occlusion cmd1s medulloblastoma amyloid deposition glioma hormone-refractory prostate cancer acute myeloid leukemia psychological stress abuse, heroin carcinoma; renal cell brain lesion reticuloendotheliosis EIA enteritis NPC alcoholism sezary syndrome derivative chromosome insulin resistance infection; mycoplasma t-all sodium retention oral lichen planus dengue PCT granulomatosis; wegener complicated pregnancy leukemia myeloid bilateral carotid artery occlusion hyperplastic nodule glomerulonephritis craniosynostosis von willebrand disorder; memory granuloma pyogenic endometrial cancer lymphoproliferative disorder bone osteosarcoma angiotensin hypertension myositis; ossificans osteofibrous dysplasia pleural mesothelioma papillomavirus infection dysplasia dysfunction; placental tumor growth fetal alcohol syndrome anaplastic astrocytoma leukemia l1210 hyperthyroidism edema lipoid nephrosis keratoconus ureteral obstruction aortic regurgitation HIE sacrococcygeal teratoma obstruction cancer hypertension pulmonary spinobulbar muscular atrophies embryonal carcinoma basal cell carcinoma growth arrest cell transformation media; otitis precancerous lesions autonomic imbalance physiological stress colorectal adenoma carotid occlusion inflammatory cell infiltration brain tumor periosteal osteosarcoma listeriosis amylacea; corpora bernard-soulier syndrome pheochromocytoma osteosarcoma; telangiectatic celiac disease hyperplasia; liver fibrosarcoma ileitis lewis lung carcinoma acute liver damage ataxia telangiectasia HI fibrillary astrocytoma response, acute phase epithelial hyperplasia skin tumor superinfection hyperplasia pigmentosum; xeroderma airway disease atherosclerotic plaque RA infarct fsgs gliosis septic shock catabolic state leukemia pathogeneses airway obstruction leukemia; monoblastic arteriosclerosis cardiac; lesion pancreatic cancer gastric ulcer maturation defect pcfcl persistent pulmonary hypertension eosinophilia polycystic kidney disease xenograft model orchitis balanced; rearrangement autoimmune invasive growth cardiomyopathies atopic dermatitis psoriatic plaque benign nevi hyperammonemia persistent infection raeb-t malignant pleural mesothelioma disease; fibroid inflammatory response tumor angiogenesis infection viral htlv-1 infection blast leukemia multiple organ dysfunction syndrome adult t-cell leukemia retinoblastoma hyperinsulinemia lesion; motor cortex iugr teratocarcinoma melanoma metastatic optic neuropathies maternal hypothyroidism ischemia carcinoma poorly differentiated cervical lesion hypomyelination schizophrenia asthma mgus SIDS allergic rhinitis shock; traumatic withdrawal seizure adenocarcinoma gastric condyloma herniated disc neurological disorder scleroderma disease; hodgkin distress deficiency; zinc gram-negative; sepsis idiopathic interstitial pneumonia primary fibrosarcoma tuberculosis proteinuria chemical carcinogenesis immunodeficiency break, single-strand dna hepatitis b psychiatric disorder leukemia monocytic vitamin e deficiencies sarcoma disease; ischemic heart hypersensitivities warts skin hyperplasia dwarf mood disorder alcohol; liver corneal infection genomic instabilities lesion; skin dermatitis amino acid deficiency invasive carcinoma carotid artery thrombosis choriomeningitis lymphocytic lead line bacterial infection liposarcoma picornavirus infection neurodegeneration food aversion chronic hepatitis c carcinoid peritonitis; septic hairy cell leukemia dedifferentiated liposarcoma ALS acute inflammatory response skeletal malformation muscle fiber hypertrophy mitochondrial damage tetraploidy erythroblastosis retinopathies tumorigenicity infarct mca infection following vaccination human parvovirus skin cancer AD pathological angiogenesis restenosis cardiac hypertrophy squamous cell carcinoma differentiated moderately leukemia lymphoid stroke human papillomavirus cerebellar dysfunction infectious autosomal dominant retinitis pigmentosa liver metastases monoarthritis ovarian tumor splenic marginal zone lymphoma measle polymyositis atrophy muscle bone metastases bronchogenic carcinoma hepatic necrosis renal tumor disorder myeloproliferative synovial sarcoma cystitis herpes simplex tumor morphology cutis laxa neurodegenerative disease facial paralysis brain death COPD hypertrophy; ventricular; left premalignant lesion gene fusion bannister malignant disease amyotrophic lateral sclerosis, sporadic estrogenic effect lesion; primary disease; liver strep lesion; nerve ovarian cancer affect alteration epithelial proliferation leiomyoma reflux atherogenesis thrombus gastric fistula glucocorticoid resistance fibrosis liver endometrial tumor insulinoma psoriasis visceral steatosis sclc immunosuppression aortic stenosis fibrous dysplasia t cell deficiency cell injury bronchiolitis lymphoma, t-cell lymph node metastasis closure; cranial sutures neoplastic transformation retinal tear hepatitis c chronic disease infection induced idiopathic pulmonary fibrosis colon cancer middle cerebral artery occlusion DSCR1 tsutsugamushi astrocytoma acute systemic lupus erythematosus thyroid cancer PBC albino gastrointestinal tumor influenza a virus infection acute lymphoblastic leukemia hepatotoxicity hypovolemic shock salmonella typhimurium infection adrenocortical carcinoma uveal melanoma retinal damage senile plaque gastritis lymphoma (non-hodgkins) central osteosarcoma carotid body tumor class ii; histocompatibility complex multiple myeloma membranous nephropathies cerebrovascular disease gingival overgrowth chronic lung disease leukemogenesis stomatitis vascular disease choriocarcinoma sepsis adult aml chronic inflammation ischemia retinal malaria basement membrane thickening erythroleukemia rheumatic disease infection; prion transient ischemia hypertrophic scar cns lesion diabetic retinopathy proliferative lung cancer lymphatic metastasis myelodysplastic syndrome aneurysm cerebral cortical; epileptic destructive arthritis damage; renal rotavirus infection amyloidosis cutaneous t-cell lymphoma bone loss hypertension ocular colon adenocarcinoma nuclear aggregate shock cerebral infarction parathyroid tumor pneumoniae colorectal cancer epilepsy temporal lobe dominant-negative mutant hnscc diabetic nephropathies rectal cancer hypertension uterine abnormalities cysts embryonal rhabdomyosarcoma hepatitis oral cancer chronic cystitis sarcoidosis vascular inflammations malignant conversion thrombosis innate immune response extravasation transitional cell tumor cardiovascular disease varicella zoster Nbs preeclampsia colon tumor huntington disease neuropathy sensory pick disease gastric cancer barrett esophagus chronic ulcer melanoma glaucoma tumor progression keloids chromosomal gain disease; protein aldosteronism primary bone tumor severe dysplasia failure; ventricular disease parkinsons obese tongue cancer disease; inflammatory bowel primary cutaneous lymphoma human immunodeficiency virus fibrosis pulmonary myocarditis clinical infection neuroendocrine carcinoma lung adenoma leydig cell tumor colon carcinoid tumor cytopathic effect deficiency; immune alveolar rhabdomyosarcoma pancreatic tumor disease; lung solid tumor chronic myeloid leukemia persistent truncus arteriosus jaundice obstructive angina unstable oral disease leukoplakia oral schwannoma cerebral ischemia neuroma mitochondrial disease intestinal cancer obstructive sleep apnea axotomy response endometrial hyperplasia osteopetrosis proliferative retinopathy spindle cell carcinoma endometriosis residual cancer aids-related kaposi sarcoma adenoma tubulovillous lung metastases liver mass giant cell tumor bladder; overactive nsclc primary tumor non-hodgkins lymphoma stage iv tumor necrosis hypodiploidy rhabdomyosarcoma break, double-strand dna occlusion; vascular adenoma; pituitary dependence; nicotine rsv infection oncogenesis acute promyelocytic leukemia cervical adenocarcinoma brain pathology atrophies polyp ulcer MS parvovirus b19 cardiomyopathy dilated fibrous histiocytoma malignant SARS bipolar disorder bladder transitional cell carcinoma endothelial dysfunction hypotensive lymphocytic infiltration murine encephalomyelitis renal ischemia cachexia; cancer edema generalized carcinogenicity withdrawal; drug atopy vulvar carcinoma intracranial glioma macronucleus disease; respiratory cytoplasmic accumulation iga nephropathies squamous cell carcinoma chromosomal instabilities damage; vascular stump pregnancy early glomerulonephritis immune complex hypertrophies diverticulitis colorectal tumor partial obstruction stasis adenoma shock syndrome; toxic cerebral hypoxia mesothelioma nucleolar enlargement congenital deficiencies squamous metaplasia gonococcal Becker muscular dystrophy dysfunction thyroid cholesteatoma middle ear lupus nephritis impairment; memory bone destruction classical hodgkin lymphoma pilocytic astrocytoma malignant transformation dcis metabolic disturbance skin carcinogenesis migraine kaposi sarcoma retrograde degeneration acute myocardial infarction dystrophy; myotonic epilepticus; status endotoxic shock SAH hypoxic squamous cell carcinoma lung cellular stress hemorrhagic shock glomerulonephritis membranoproliferative ameloblastoma death (sudden) cancer cell growth adenocarcinoma cholestasis tumor; wilms neck cancer mucoepidermoid carcinoma abnormal; membranes brain; ischemic leukoplakia basophilic leukemia hypercalcemia acute pancreatitis inflammation acute glomerulonephritis malnutrition, protein-energy absence seizure hyperhomocysteinemia vascular calcification acid; intoxication morris hepatoma neural tube defect prostate cancer cyst; renal acute colitis lymphomatoid papulosis carcinoma hepatocellular pancreatic adenocarcinoma spinocerebellar ataxia type 7 glioblastoma adjuvant arthritis disease; skin dysplasia; epithelial corneal neovascularization junin epilepsy; partial disease; legionnaires high-grade cin anaplastic lymphoma bladder cancer warm ischemia cold ischemia lipid deposition demyelination cholesteatoma deficiency; iodine osteoarthritis fibrin deposition laryngeal carcinoma neutrophil migration epidermal hyperplasia coal worker pneumoconiosis cataract brain edema breast tumor transient cerebral ischemia pulmonary tuberculosis nuclear accumulation furfur invasive ductal carcinoma influenza uremia class i; histocompatibility complex thyroid cancer (follicular cell) renal disease progressive retina; ischemic gestational trophoblastic disease osteosclerosis nephropathies vitamin a deficiencies acute hepatitis adrenal tumor metastatic osteosarcoma retinal neovascularization enteropathy esophageal cancer iron overload chronic pain cholera synovitis b virus infection myocardial reperfusion injuries arthritis hypothyroid
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