ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation. - Wikidata - wikimedia - TriplyDB

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

http://www.wikidata.org/entity/Q34398844

about

A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation.METTL23, a transcriptional partner of GABPA, is essential for human cognition.High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.Adaptive evolution in zinc finger transcription factors.The ancient mammalian KRAB zinc finger gene cluster on human chromosome 8q24.3 illustrates principles of C2H2 zinc finger evolution associated with unique expression profiles in human tissues.Differences in human and chimpanzee gene expression patterns define an evolving network of transcription factors in brain Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome.The genetic basis of non-syndromic intellectual disability: a review CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592 Exome sequencing identifies three novel candidate genes implicated in intellectual disability Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?High-resolution genomic microarrays for X-linked mental retardation.Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene.Positional plasticity in regenerating Amybstoma mexicanum limbs is associated with cell proliferation and pathways of cellular differentiation.A large scale multivariate parallel ICA method reveals novel imaging-genetic relationships for Alzheimer's disease in the ADNI cohort.Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region.X-linked mental retardation and epigenetics.A new chromosome x exon-specific microarray platform for screening of patients with X-linked disorders.Making headway with genetic diagnostics of intellectual disabilities.MicroRNA-181a modulates gene expression of zinc finger family members by directly targeting their coding regions.Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?Genomic characterization of chromosome 8 pericentric trisomy.Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population.Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations.Sex chromosome aneuploidies and copy-number variants: a further explanation for neurodevelopmental prognosis variability?

P2860

Q24304870-BE4AB2DD-E96D-429B-9801-536588E46F27 Q24632796-13DF3951-1DC3-4BA9-AE2E-5B9E4FDCF542 Q24669780-FACF169B-A637-4CAC-83D4-585371FA6BA8 Q24681478-663BA11B-A74F-4D0E-ABFD-E7BBB2F7A286 Q30179391-F70A284C-B125-4018-AFF2-8B3E2290F567 Q30496457-E4BBD0FA-AB20-45C6-A1ED-CD806EBC8342 Q33387075-35754A72-491E-499F-A33B-EEC08D3F2E32 Q33396985-350124AF-3264-41F3-844E-7C02DE0DBD3C Q33546685-A08A51D1-9925-4A94-942C-4695AE487858 Q33564055-E2A388E1-3B5F-4CFB-BAB2-8693542C87E7 Q33803380-8F2EF64F-B730-4FA0-B175-80DA38AD1926 Q34283901-5DB50F6E-FFE8-48FB-9920-C48D4EC72893 Q34329675-33742A9E-BB78-4740-A5CE-8DC214F52B85 Q34535723-A3B5FF48-4FC4-4C1A-9156-251FD81C0EB3 Q34554504-EEC3DE6F-14A7-4768-AD17-84E09272866F Q34688430-B3D9DBA5-6EC2-4AA9-9AD7-65B12AA1FCB4 Q35444663-B6A2D05C-E1F6-4ACA-8115-92B0B90D4334 Q35849238-3FBEEBB8-A5AB-4C30-B899-FC2F1121B49D Q35854717-D06BC07A-D6F1-4FA5-BE63-63D81D2B94A9 Q36287023-34C59631-F746-4A3A-8073-6841338C27B0 Q36663018-57234F76-5E4A-441D-A1C8-2AB056DB1B17 Q37396260-0A746CC8-DB7F-47BA-B7BC-F54BA55D5F6A Q38124929-E33055D7-D7CD-4622-9E97-5DEA67F52C0F Q39686536-0414E580-00E6-4DA3-A690-F77E41EEA305 Q41342635-A55D3A4D-5729-4A59-8849-AA8D79AE9858 Q42424835-9B4CB192-BB63-47F6-B355-8627A7C73FE8 Q44944494-DB219912-902E-4CCD-8AF2-2ADEA76EA19E Q46242568-030356B7-FDA4-4E51-8E04-15189C32473A Q48278517-27A9F444-8D71-4320-BA0A-5D125F9CB18E Q48280356-66834E8B-9978-4ECB-B253-40FFE99C6594

P2860

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

http://www.wikidata.org/entity/Q34398844

description

2005 nî lūn-bûn

@nan

2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@ast

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@en

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@nl

type

label

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@ast

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@en

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@nl

prefLabel

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@ast

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@en

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@nl

P1433

Q34398844-4533B04A-1ADA-4C03-9977-C13B546B3377

P1476

Q34398844-0C35B441-408F-4A3F-AF6F-A41F8E7C2309

P2093

Q34398844-0BC4C5CC-0E7D-4C97-94B1-EE138245DEA3

Q34398844-10DFF64E-03FD-4B10-B8C0-9FC6B85234C4

Q34398844-127D114B-9845-471B-AAFE-8660C6B77960

Q34398844-298C4D3E-3F07-4F54-97A1-A9EE51A770EB

Q34398844-3CC1FB61-8A7B-4653-9D1E-A5C9FCDA4ED5

Q34398844-554B9CB7-B196-4174-B099-801C88459EB4

Q34398844-8536721F-F47D-4DAC-A2BC-BE94F10AF146

Q34398844-89658347-0F7C-4D17-AAE6-12C52453C770

Q34398844-8F24F3F0-84CE-4F48-8591-CC7B18F661EA

Q34398844-8F92CE73-88C0-479A-898E-77CBFC238264

P2860

Q34398844-020A7878-83BA-4EA5-8DC5-BDA6D51C5D99

Q34398844-08B0555F-C7FA-44E1-A726-45D85861CFBF

Q34398844-093CF7A7-9F3B-4938-AA97-3B73DC11F92A

Q34398844-1231E94F-5B1F-4E04-A64A-9E23ACA55394

Q34398844-1F906402-2258-4DAD-90E1-BEEE69C79751

Q34398844-22A39589-7C50-4644-8EFE-EA079F061713

Q34398844-26720187-7AF5-4C54-B57A-20E7E9A6A721

Q34398844-2839C11B-2093-496C-917B-386CD8C2951E

Q34398844-34F67A66-1514-450A-80AB-ABE40EF07E2D

Q34398844-42199512-3DC0-456B-9871-6EAAC56D49F3

P304

Q34398844-2352FD8B-2C07-4D49-9FB2-65357EB7B2B7

P31

Q34398844-9C4C47ED-177D-41BF-AAA5-61A90CF26CE3

P356

Q34398844-7E7C85A0-2B79-4E37-A86D-4FB19A8C992E

P407

Q34398844-1AEC4777-FABA-46BE-8572-CDE783934E95

P433

Q34398844-7E245BE4-CF64-4015-B5B3-7055881EE713

P478

Q34398844-DEBB738E-422F-421C-BCC2-A7D7C9E7662B

P50

Q34398844-0485CC10-3E94-4B30-BB1E-1E98FB5C458A

Q34398844-724C5432-3182-4431-B606-BF04139E8B9F

P577

Q34398844-C891735C-0173-4FB5-B75A-311F4DD83270

P5875

Q34398844-2954000B-A930-4848-A6E1-8390E76A21B0

P698

Q34398844-60E4CAAD-5481-4FCB-9859-AF4DC6D0F2EB

P932

Q34398844-B1D569D9-9D89-496E-9771-96EC2F76820E

P356

P1433

American Journal of Human Genetics

P1476

ZNF674: a new kruppel-associat ...... c X-linked mental retardation.

@en

P2093

Arjan P M de Brouwer

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

Astrid R Oudakker

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

Ben C J Hamel

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

Bert B A de Vries

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

Claude Moraine

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

Dorien Lugtenberg

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

Hans van Bokhoven

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

Hans-Hilger Ropers

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

Helen V Firth

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

Helger G Yntema

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

P2860

MUSCLE: a multiple sequence alignment method with reduced time and space complexity

KAP-1 corepressor protein interacts and colocalizes with heterochromatic and euchromatic HP1 proteins: a potential role for Krüppel-associated box-zinc finger proteins in heterochromatin-mediated gene silencing.

A novel nuclear receptor corepressor complex, N-CoR, contains components of the mammalian SWI/SNF complex and the corepressor KAP-1

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

The evolutionarily conserved Krüppel-associated box domain defines a subfamily of eukaryotic multifingered proteins

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

KAP-1, a novel corepressor for the highly conserved KRAB repression domain

Cloning and characterization of a novel zinc finger gene in Xp11.2

Positional cloning of the gene for X-linked retinitis pigmentosa 2

Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation.

P304

265-278

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

P31

scholarly article

P356

10.1086/500306

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

P407

P433

2

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

P478

78

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

P50

Martine Raynaud

P577

2005-12-29T00:00:00Z

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

P5875

7386821

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

P698

16385466

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

P932

1380234

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