About: A novel human gene FKBP6 is deleted in Williams syndrome

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About: A novel human gene FKBP6 is deleted in Williams syndrome Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu espublizáu en 1998 (ast) vědecký článek publikovaný v roce 1998 (cs) 1998 թվականի սեպտեմբերին հրատարակված գիտական հոդված (hy) مقالة علمية (نشرت في سبتمبر 1998) (ar) 1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 1998/09/01) (sk) наукова стаття, опублікована у вересні 1998 (uk) научни чланак (објављен 1998/09/01) (sr) wetenschappelijk artikel (gepubliceerd op 1998/09/01) (nl) im September 1998 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28116736-8CB7466C-8B04-4C3C-B0BD-F2B14783E5BF
publication date	1998-09-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q28116736-052D7EFA-63B9-4088-8539-BC0BE67191AD wds:Q28116736-0E296B44-58CE-4B65-8790-5D86385B0095 wds:Q28116736-45ED6111-9EA5-4167-B447-E832106D63F7
author name string	X. Meng X. Lu M. T. Keating
rdfs:label	A novel human gene FKBP6 is deleted in Williams syndrome (en) A novel human gene FKBP6 is deleted in Williams syndrome (nl) A novel human gene FKBP6 is deleted in Williams syndrome (ast)
skos:prefLabel	A novel human gene FKBP6 is deleted in Williams syndrome (en) A novel human gene FKBP6 is deleted in Williams syndrome (nl) A novel human gene FKBP6 is deleted in Williams syndrome (ast)
name	A novel human gene FKBP6 is deleted in Williams syndrome (en) A novel human gene FKBP6 is deleted in Williams syndrome (nl) A novel human gene FKBP6 is deleted in Williams syndrome (ast)
author	wds:Q28116736-4fbc1cf2-47be-92eb-3a39-e991ce4b4a2f
author	Colleen A. Morris
title	wds:Q28116736-6AB2D57E-B6F8-4F7D-BD38-595B4A024549
title	A novel human gene FKBP6 is deleted in Williams syndrome (en)
page(s)	wds:Q28116736-6AA0A1EA-F999-4069-BE63-DFF89E803FC1
page(s)	130–137
instance of	wds:Q28116736-96E7D39E-7B4F-41DE-B767-25C9877AF1A3
instance of	scholarly article
main subject	wds:Q28116736-71787920-7186-458B-8616-BD646C4CA694 wds:Q28116736-82763D9E-AB1C-486A-845E-2D269066AE09
main subject	FK506 binding FKBP prolyl isomerase 6
PubMed ID	wds:Q28116736-8F4B5791-3859-4072-AD0E-784B09B8F70D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9782077
PubMed ID	9782077
published in	wds:Q28116736-3B51AE90-904F-4EB0-8F35-7AC51D42866B
published in	Genomics
issue	wds:Q28116736-DC975E64-0EFD-4608-ABD9-8597A93BF082
volume	wds:Q28116736-44D244B8-4F0B-4D48-9971-7DA7C98462C7
issue	2
volume	52
DOI	wds:Q28116736-EFF1812E-B7A2-4E6C-90A7-9B07F899F763
DOI	http://dx.doi.org/10.1006/GENO.1998.5412
DOI	10.1006/GENO.1998.5412
Fatcat ID	wds:Q28116736-3B42E63E-EE62-4B0E-BE2E-322C0450392F
Fatcat ID	release_6yjfvenegjbthnp5gecz22whby
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28116736
is cites work of	Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23 Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis Biochemical analysis of mouse FKBP60, a novel member of the FKPB family A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome Regulation of peptide bond cis/trans isomerization by enzyme catalysis and its implication in physiological processes Tetratricopeptide repeat cochaperones in steroid receptor complexes Functional diversity and pharmacological profiles of the FKBPs and their complexes with small natural ligands Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome C-terminal sequences outside the tetratricopeptide repeat domain of FKBP51 and FKBP52 cause differential binding to Hsp90. VI. Genome structure and cognitive map of Williams syndrome Receptor accessory folding helper enzymes: the functional role of peptidyl prolyl cis/trans isomerases Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I Sequence diversification of the FK506-binding proteins in several different genomes. Copy number variants at Williams-Beuren syndrome 7q11.23 region. Dissecting the mammalian synaptonemal complex using targeted mutations. Mouse lysocardiolipin acyltransferase controls the development of hematopoietic and endothelial lineages during in vitro embryonic stem-cell differentiation Calcineurin regulation in fungi and beyond A novel anti-inflammatory drug, SDZ ASM 981, for the treatment of skin diseases: in vitro pharmacology The human FK506-binding proteins: characterization of human FKBP19 Implication of FKBP6 for male fertility in horses. Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression Williams syndrome: an update on clinical and molecular aspects Peptidyl-prolyl isomerases: a full cast of critical actors in cardiovascular diseases. A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23 Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations FKBP36 is an inherent multifunctional glyceraldehyde-3-phosphate dehydrogenase inhibitor FK506-Binding Proteins and Their Diverse Functions Genome-wide methylation profiling reveals Zinc finger protein 516 (ZNF516) and FK-506-binding protein 6 (FKBP6) promoters frequently methylated in cervical neoplasia, associated with HPV status and ethnicity in a Chilean population Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder Functions of the Hsp90-binding FKBP immunophilins. Is a genetic defect in Fkbp6 a common cause of azoospermia in humans? Genome-wide association study implicates testis-sperm specific FKBP6 as a susceptibility locus for impaired acrosome reaction in stallions Involvement of FKBP6 in hepatitis C virus replication The shut-down gene of Drosophila melanogaster encodes a novel FK506-binding protein essential for the formation of germline cysts during oogenesis Identification of residues in the TPR domain of Ssn6 responsible for interaction with the Tup1 protein Separation and identification of differentially expressed nuclear matrix proteins between human esophageal immortalized and carcinomatous cell lines Differential DNA methylation of the meiosis-specific gene FKBP6 in testes of yak and cattle-yak hybrids Injury prevention Compression of Large Sets of Sequence Data Reveals Fine Diversification of Functional Profiles in Multigene Families of Proteins: A Study for Peptidyl-Prolyl Isomerases (PPIase)
is cites work of	wds:Q24291167-528B0644-DD82-41E3-89CA-18ADAD2DB080 wds:Q35264833-71997F03-4C30-4F42-9F51-192998C68F54 wds:Q38489415-F16F6F47-CB4A-4F28-85DD-4E9FB9D37AF1

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