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Author Details
Full Name
Arnaud Gos
Affiliation
Centre Medical Universitaire
ORCID
Career Start Year
1992
Papers
22
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36866529
The Gene Ontology knowledgebase in 2023.
Genetics
2023
32716361
A Coordinated Approach by Public Domain Bioinformatics Resources to Aid the Fight Against Alzheimer's Disease Through Expert Curation of Key Protein Targets.
J Alzheimers Dis
2020
24848695
Genetic variations and diseases in UniProtKB/Swiss-Prot: the ins and outs of expert manual curation.
Hum Mutat
2014
23161678
Gene Ontology annotations and resources.
Nucleic Acids Res
2013
22123736
The UniProt-GO Annotation database in 2011.
Nucleic Acids Res
2012
18175334
Annotating single amino acid polymorphisms in the UniProt/Swiss-Prot knowledgebase.
Hum Mutat
2008
10598804
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y.
Hum Genet
1999
10393427
Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping.
Cytogenet Cell Genet
1999
10049735
Isolation and characterization of the mouse Aire gene.
Biochem Biophys Res Commun
1999
9826911
Gene structure and chromosomal localization of the human P2X7 receptor.
Recept Channels
1998
9032654
Fortuitous detection of uniparental isodisomy of chromosome 6.
J Med Genet
1997
9188657
Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.
Am J Med Genet
1997
9401005
Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency.
Hum Mutat
1997
8660980
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.
Genomics
1996
8812505
Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter.
Genomics
1996
8660983
Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21.
Genomics
1996
7644464
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
Proc Natl Acad Sci U S A
1995
8834001
Characterization and chromosomal localization of a human P2X receptor from the urinary bladder.
Recept Channels
1995
7762575
Schizophrenia and chromosomal deletions within 22q11.2.
Am J Hum Genet
1995
7668265
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.
Am J Hum Genet
1995
7647800
Single-minded and Down syndrome?
Nat Genet
1995
1426044
Polarized secretion of urokinase-type plasminogen activator by epithelial cells.
Exp Cell Res
1992
1 - 22 of 22
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