About: Jeffrey Trent

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

American geneticist

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) изилдөөчү (ky) 研究者 (zh) American geneticist (en) genetista estadounidense (es) عالم وراثة أمريكي (ar) geneticus (nl) amerykański genetyk (pl)
rdfs:label	Jeffrey M Trent (nl) Jeffrey Trent (en) Jeffrey Trent (es) Jeffrey Trent (pl) Jeffrey Trent (sq) Jeffrey Trent (ast)
skos:prefLabel	Jeffrey M Trent (nl) Jeffrey Trent (en) Jeffrey Trent (es) Jeffrey Trent (pl) Jeffrey Trent (sq) Jeffrey Trent (ast)
name	Jeffrey M Trent (nl) Jeffrey Trent (en) Jeffrey Trent (es) Jeffrey Trent (pl) Jeffrey Trent (sq) Jeffrey Trent (ast)
Freebase ID	wds:Q28033905-A3D0442A-3199-41CA-8EA9-E3CC5C9634C8
Freebase ID	/m/030p60h
given name	wds:Q28033905-4265B2BF-63BA-4B18-A16B-BC8E65EE2695
given name	Jeffrey
instance of	wds:Q28033905-4FEB84B9-2E2D-48ED-818E-49441D21C186
instance of	Homo sapiens
skos:altLabel	Trent (en) J M Trent (en) J Trent (en) J. M. Trent (en) J. Trent (en) Jeffrey M Trent (en) Jeffrey M. Trent (en) Trent J (en) Trent J M (en) Trent J. (en) Trent J. M. (en) Trent JM (en)
occupation	wds:Q28033905-AFA1F1FE-013D-4AA3-AE52-40B38034934B wds:Q28033905-cfd38649-e8bc-4653-97f0-01696108adf8
employer	wds:Q28033905-5d9b0883-078a-4bb5-ba29-79c051ac2e7d
sex or gender	wds:Q28033905-F2C6B0D1-1515-4D2C-A4D3-81B362EEF402
family name	wds:Q28033905-3BADF43E-14F3-4308-B00E-38B1B01E37E9
occupation	researcher geneticist
employer	University of Michigan
sex or gender	male
family name	Trent
ORCID iD	wds:Q28033905-EBB64C42-D969-42B0-B7FD-9972836F25D7
ORCID iD	https://orcid.org/0000-0003-0183-4202
ORCID iD	0000-0003-0183-4202
is owl:sameAs of	Jeffrey Trent
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28033905 Jeffrey Trent
is author of	A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population Wnt5a signaling directly affects cell motility and invasion of metastatic melanoma A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma High frequency of BRAF mutations in nevi Gene-expression profiling in human cutaneous melanoma Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicine Advancing a clinically relevant perspective of the clonal nature of cancer Functional evidence implicating S100P in prostate cancer progression Gene expression signature of benign prostatic hyperplasia revealed by cDNA microarray analysis Identification and characterization of mouse Rab32 by mRNA and protein expression analysis GeneLink: a database to facilitate genetic studies of complex traits Molecular classification of familial non-BRCA1/BRCA2 breast cancer Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1. Genome‐wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26. Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease Which is better for cDNA-microarray-based classification: ratios or direct intensities. Generation and analysis of melanoma SAGE libraries: SAGE advice on the melanoma transcriptome Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13 Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk Toward precision medicine in glioblastoma: the promise and the challenges Proteasome inhibitors trigger NOXA-mediated apoptosis in melanoma and myeloma cells Development of potent autophagy inhibitors that sensitize oncogenic BRAF V600E mutant melanoma tumor cells to vemurafenib Molecular determinants of human uveal melanoma invasion and metastasis. Looking beyond morphology: cancer gene expression profiling using DNA microarrays Common sequence variants on 20q11.22 confer melanoma susceptibility Identification of combination gene sets for glioma classification. Synthetic lethal RNAi screening identifies sensitizing targets for gemcitabine therapy in pancreatic cancer Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 Inference from clustering with application to gene-expression microarrays Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4 Dual loss of the SWI/SNF complex ATPases SMARCA4/BRG1 and SMARCA2/BRM is highly sensitive and specific for small cell carcinoma of the ovary, hypercalcaemic type. Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing The Wnt5A/protein kinase C pathway mediates motility in melanoma cells via the inhibition of metastasis suppressors and initiation of an epithelial to mesenchymal transition. Alpha-methylacyl-CoA racemase: a new molecular marker for prostate cancer.

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