Systematic discovery of nonobvious human disease models through orthologous phenotypes - Wikidata - awgldk - TriplyDB

Systematic discovery of nonobvious human disease models through orthologous phenotypes

Systematic discovery of nonobvious human disease models through orthologous phenotypes

http://www.wikidata.org/entity/Q24600277

about

Evolutionarily repurposed networks reveal the well-known antifungal drug thiabendazole to be a novel vascular disrupting agent Mouse genetic and phenotypic resources for human genetics FlyBase portals to human disease research using Drosophila models Translational bioinformatics: linking the molecular world to the clinical world Structure and dynamics of molecular networks: a novel paradigm of drug discovery: a comprehensive review Cross-Species Integrative Functional Genomics in GeneWeaver Reveals a Role for Pafah1b1 in Altered Response to Alcohol.A yeast phenomic model for the gene interaction network modulating CFTR-ΔF508 protein biogenesis.Applications of comparative evolution to human disease genetics A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases Functional profiling discovers the dieldrin organochlorinated pesticide affects leucine availability in yeast Signalogs: orthology-based identification of novel signaling pathway components in three metazoans Global analysis of small molecule binding to related protein targets Prediction and validation of gene-disease associations using methods inspired by social network analyses A viral-human interactome based on structural motif-domain interactions captures the human infectome 'Death and axes': unexpected Ca²⁺ entry phenologs predict new anti-schistosomal agents Comparative genomic analysis of slc39a12/ZIP12: insight into a zinc transporter required for vertebrate nervous system development Neurulation and neurite extension require the zinc transporter ZIP12 (slc39a12)The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species p125/Sec23-interacting protein (Sec23ip) is required for spermiogenesis Efforts to make and apply humanized yeast Yeast Augmented Network Analysis (YANA): a new systems approach to identify therapeutic targets for human genetic diseases Toward knowledge support for analysis and interpretation of complex traits Prediction of gene-phenotype associations in humans, mice, and plants using phenologs Human brain evolution: harnessing the genomics (r)evolution to link genes, cognition, and behavior Laboratory mouse models for the human genome-wide associations Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders A future of the model organism model Phenotype ontologies and cross-species analysis for translational research Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes Gene-class analysis of expression patterns induced by psychoactive pharmaceutical exposure in fathead minnow (Pimephales promelas) indicates induction of neuronal systems.Joint mouse-human phenome-wide association to test gene function and disease risk.Worm Phenotype Ontology: integrating phenotype data within and beyond the C. elegans community.Boosting signal-to-noise in complex biology: prior knowledge is power The ortholog conjecture is untestable by the current gene ontology but is supported by RNA sequencing data.WormQTLHD--a web database for linking human disease to natural variation data in C. elegans.Functional toxicology: tools to advance the future of toxicity testing.Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans Using association rule mining to determine promising secondary phenotyping hypotheses Gene set enrichment analysis of microarray data from Pimephales promelas (Rafinesque), a non-mammalian model organism Saccharomyces cerevisiae as a model organism: a comparative study

P2860

Q21145736-C66BCD11-038A-4763-8826-A75CB457A0A2 Q24628817-14711AC4-867B-44A0-9F65-DD56EC87251F Q26765019-64964511-B814-4570-9D48-F5737837BE45 Q27002440-DC2D81AB-4232-40F7-9493-EAF8B5157D3C Q27008867-FDD9AB20-B610-4847-B1F0-74B397B97B67 Q27321572-BF97BE8B-249E-4E07-94E4-85E4CB7E9C50 Q27931694-FC151C8A-4C8F-45C8-9D90-9B2333487D4A Q28083558-C3EDE2C7-B0C5-4447-8778-50C147762C70 Q28114951-F18E267D-6D87-4178-847A-883C63337FDE Q28395538-9A923E9B-FA90-47A1-B4E1-1377DF1F3E3B Q28478034-CB028C13-C0B5-4018-AA50-22BA6A9DE7C2 Q28478884-925B8457-E7F6-4A73-8DA7-3E7B946FD67C Q28487430-DABE26BA-DCA8-44D7-B233-57F8EA1C51B5 Q28535207-1399124E-C27A-4E1F-9EB3-844A0252E255 Q28539960-6D5C7990-50DE-441E-9B7E-8D886C17ED96 Q28544773-8F3A5101-F8FA-4D52-9392-982CA904F159 Q28576491-245DDC3D-BB48-4031-B14D-A40AE5D88670 Q28584446-1EFE531C-9681-421A-BC1C-23FF771CC031 Q28590059-02319CB7-0A1D-4155-9739-22DE344B22E2 Q28602193-4AAE4F44-AF58-4FB0-AA96-5327B7C05BDE Q28655730-056C239B-0F16-4DA2-B536-C16131247D16 Q28658388-E935D523-FAC7-4E7C-AA99-85D59B276388 Q28679989-98F2DC1C-92CD-4473-857F-20074411479A Q28744614-5C3AC224-0D57-4FD0-9568-920653C802D4 Q28748647-CF402500-DF1F-4446-ABC3-1C262710EEC7 Q29396093-436496E9-346D-426B-A3E7-E6776FC3D1BE Q30413054-E528C252-861B-491B-9E60-56C907D34E22 Q30440406-D75163A1-5248-43B1-BCDF-3A761AA08234 Q30454026-AA9812CA-B501-409B-9C0B-B3F5024C08C8 Q30459493-1CE64325-6C03-4CD3-ACE2-1C797C0B0BC2 Q30488888-64DC9385-F0CF-44CE-B838-D5D25215981F Q30498190-301A6D8C-DA99-420C-B359-05E39CB3ECEA Q30500493-3A716FEA-563C-4EFE-B8CD-9F4BF105637F Q30580058-EFC4C4AC-CF8C-434B-B9EB-3B1C912546B7 Q30692701-FB096362-C74B-4525-A825-BDB9BBE9485D Q33595247-23B4ADF7-0C66-4952-9092-95B6903BFB29 Q33710573-EDAFE4AD-9ACD-4ABD-9AF8-7E175CECCB95 Q33760921-5E0F8F43-832F-4702-9DF8-41BCD711234F Q33804405-6DAAFA26-E228-4BD7-B393-C8D3EBEE70B8 Q33818079-38146758-3E0F-425A-A55B-2305269E5534

P2860

Systematic discovery of nonobvious human disease models through orthologous phenotypes

http://www.wikidata.org/entity/Q24600277

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@ast

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@en

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@nl

type

label

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@ast

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@en

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@nl

prefLabel

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@ast

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@en

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@nl

P1433

Q24600277-C8EFEE8B-887F-43B4-A927-546E6F496BEE

P1476

Q24600277-7BDE2728-D921-4BC7-A471-12C6C8016498

P2093

Q24600277-46918F33-C099-4458-AF33-EF3F155E17EC

Q24600277-B2F91F27-2AEF-44C0-A2F9-484F9C9C17F0

Q24600277-B40F5BB2-2A3B-4913-B842-B0B37DF94794

Q24600277-E03441C1-F25B-4F67-A022-66AD07E984B9

P2860

Q24600277-1FA017C2-F152-4349-87DA-82A7719EA767

Q24600277-262901DC-42AC-4501-BAE9-013AE572A78E

Q24600277-2E6CEB3D-61ED-4596-9C6C-448F18FC0588

Q24600277-312CD1BD-B484-4E8C-8BBB-A15F9208C7C4

Q24600277-456B00BE-5A95-4E69-9BCD-135325A33E81

Q24600277-45DF2531-6735-4F00-BA75-A46BA0691F2F

Q24600277-60926345-7BF1-4E17-A188-FB1B9E06DE52

Q24600277-61EA346F-E2FC-4F39-88D6-F9AB8756E101

Q24600277-69E45459-B1CC-4140-B8D2-118B5AA9488C

Q24600277-759839BE-9478-4873-88F7-6671D0B42945

P304

Q24600277-162109AD-3CE7-4B7A-A75D-7410C3226BEB

P31

Q24600277-4C7248CC-97BE-40DA-B1B0-FD6E5A3B42E6

P3181

Q24600277-CD1FE1AA-1C80-440D-85A8-DEF2E4079450

P356

Q24600277-A1B3E5B1-781A-4670-A000-3A23FB5DEB94

P407

Q24600277-61F7FD54-12C9-4CC6-9077-C0C40327BE73

P433

Q24600277-A29A0762-4534-429B-919E-F1FEBA294BB3

P478

Q24600277-027647AA-8C54-4DB9-8739-C1DF723A9D2B

P50

Q24600277-5206E5E1-5E15-41A3-8A89-07B8B26A91D2

P577

Q24600277-7865F55B-8582-4867-AE97-0AAAD2EEE78A

P5875

Q24600277-3174EB2B-224D-41C6-B2C3-B08DA704B726

P698

Q24600277-DB9790F9-A776-407E-9FC1-79EE051C46CE

P932

Q24600277-1A7DB056-ACC0-4F98-91AA-2B2B53716DD0

P3181

P356

PNAS.0910200107

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Systematic discovery of nonobvious human disease models through orthologous phenotypes

@en

P2093

Hye Ji Cha

http://www.w3.org/2001/XMLSchema#string

John B Wallingford

http://www.w3.org/2001/XMLSchema#string

John O Woods

http://www.w3.org/2001/XMLSchema#string

Kriston L McGary

http://www.w3.org/2001/XMLSchema#string

P2860

The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency

Deep homology and the origins of evolutionary novelty

Erk5 null mice display multiple extraembryonic vascular and embryonic cardiovascular defects

High expression of the HMG box factor sox-13 in arterial walls during embryonic development

Saccharomyces Genome Database (SGD) provides secondary gene annotation using the Gene Ontology (GO)

WormBase: a comprehensive data resource for Caenorhabditis biology and genomics

X chromosomal abnormalities in basal-like human breast cancer

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

McKusick's Online Mendelian Inheritance in Man (OMIM)

Automatic clustering of orthologs and in-paralogs from pairwise species comparisons

P304

6544-9

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

358504

http://www.w3.org/2001/XMLSchema#string

P356

10.1073/PNAS.0910200107

http://www.w3.org/2001/XMLSchema#string

P407

P433

14

http://www.w3.org/2001/XMLSchema#string

P478

107

http://www.w3.org/2001/XMLSchema#string

P50

P577

2010-04-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

42389557

http://www.w3.org/2001/XMLSchema#string

P698

20308572

http://www.w3.org/2001/XMLSchema#string

P932

2851946

http://www.w3.org/2001/XMLSchema#string