Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1
about
Role for the nuclear receptor-binding SET domain protein 1 (NSD1) methyltransferase in coordinating lysine 36 methylation at histone 3 with RNA polymerase II functionFibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencingCharacterization of FIM-FGFR1, the fusion product of the myeloproliferative disorder-associated t(8;13) translocationMethylation of ZNF261 as an assay for determining X chromosome inactivation patternsCell death inhibiting RNA (CDIR) derived from a 3'-untranslated region binds AUF1 and heat shock protein 27A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexesCrypton transposons: identification of new diverse families and ancient domestication eventsDisease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.ZNF198 stabilizes the LSD1-CoREST-HDAC1 complex on chromatin through its MYM-type zinc fingersX-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypesFruit flies and intellectual disability.Assembly and interrogation of Alzheimer's disease genetic networks reveal novel regulators of progressionCharacterization of the SUMO-binding activity of the myeloproliferative and mental retardation (MYM)-type zinc fingers in ZNF261 and ZNF198Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism.Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.Next-generation sequencing in X-linked intellectual disability.Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.Next-generation sequencing reveals the secrets of the chronic lymphocytic leukemia genome.Broad spectrum identification of cellular small ubiquitin-related modifier (SUMO) substrate proteins.Gene knockout of Zmym3 in mice arrests spermatogenesis at meiotic metaphase with defects in spindle assembly checkpoint.Drosophila HP1c isoform interacts with the zinc-finger proteins WOC and Relative-of-WOC to regulate gene expressionZMYM3 regulates BRCA1 localization at damaged chromatin to promote DNA repair.dDsk2 regulates H2Bub1 and RNA polymerase II pausing at dHP1c complex target genes.Disease-gene discovery by integration of 3D gene expression and transcription factor binding affinities.Skewing of the genetic architecture at the ZMYM3 human-specific 5' UTR short tandem repeat in schizophrenia.Caught with One's Zinc Fingers in the Genome Integrity Cookie Jar.Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation.X-linked mental retardation
P2860
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P2860
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1
description
1996 nî lūn-bûn
@nan
1996 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Cloning and characterization o ...... d mental retardation in Xq13.1
@ast
Cloning and characterization o ...... d mental retardation in Xq13.1
@en
Cloning and characterization o ...... d mental retardation in Xq13.1
@nl
type
label
Cloning and characterization o ...... d mental retardation in Xq13.1
@ast
Cloning and characterization o ...... d mental retardation in Xq13.1
@en
Cloning and characterization o ...... d mental retardation in Xq13.1
@nl
prefLabel
Cloning and characterization o ...... d mental retardation in Xq13.1
@ast
Cloning and characterization o ...... d mental retardation in Xq13.1
@en
Cloning and characterization o ...... d mental retardation in Xq13.1
@nl
P2093
P356
P1476
Cloning and characterization o ...... d mental retardation in Xq13.1
@en
P2093
C Philippe
F P Cremers
H H Ropers
I H Scholten
R F Suijkerbuijk
S Gilgenkrantz
S M van der Maarel
P304
P356
10.1093/HMG/5.7.887
P407
P50
P577
1996-07-01T00:00:00Z