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ZMYM3 gene
Known as:
zinc finger MYM-type containing 3
, MYM
, Zinc Finger, MYM-Type 3 Gene
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This gene is involved in chromatin modification.
National Institutes of Health
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Related topics
Related topics
5 relations
Cytoskeletal Modeling
Histone Deacetylation
Regulation of Cell Shape
chromatin remodeling
Narrower (1)
ZMYM3 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Skewing of the genetic architecture at the ZMYM3 human-specific 5′ UTR short tandem repeat in schizophrenia
Fatemeh Alizadeh
,
A. Bozorgmehr
,
J. Tavakkoly-Bazzaz
,
Mina Ohadi
Zeitschrift für Induktive Abstammungs- und…
2018
Corpus ID: 21656666
Differential expansion of a number of human short tandem repeats (STRs) at the critical core promoter and 5′ untranslated region…
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2016
2016
Die Bedeutung von ZNF261 und der Lysin-spezifischen Demethylase LSD1 in der Androgenrezeptor-abhängigen und -unabhängigen Kanzerogenese
M. Bossart
2016
Corpus ID: 78783202
2015
2015
Chronic lymphocytic leukemia: looking into the dark side of the genome
R. Valdés-Mas
,
J. Gutiérrez-Abril
,
X. S. Puente
,
C. López-Otín
Cell Death and Differentiation
2015
Corpus ID: 13473986
The International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA) have recently reported in Nature their…
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2014
2014
BMI1 reprogrammes histone acetylation and enhances c-fos pathway via directly binding to Zmym3 in malignant myeloid progression
Hongjie Shen
,
Zi X. Chen
,
+5 authors
Yan Chen
Journal of Cellular and Molecular Medicine
2014
Corpus ID: 10234912
The polycomb group BMI1 is proved to be crucial in malignant myeloid progression. However, the underlying mechanism of the action…
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2014
2014
Mutation and expression analysis in medulloblastoma yields prognostic variants and a putative mechanism of disease for i17q tumors
G. Bien-Willner
,
R. Mitra
Acta Neuropathologica Communications
2014
Corpus ID: 7395256
Current consensus identifies four molecular subtypes of medulloblastoma (MB): WNT, sonic hedgehog (SHH), and groups “3/C” and “4…
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2005
2005
First case report of X linked dystonia parkinsonism (XDP) or ‘lubag’ in Australia
C. Plummer
,
J. Bradfield
,
A. Singleton
,
D. Hernández
,
A. Singleton
,
J. O'Sullivan
Journal of clinical neuroscience
2005
Corpus ID: 36002992
2004
2004
Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X‐linked mental retardation associated with other neurological dysfunction
Todd Zorick
,
S. Kleimann
,
A. Sertié
,
M. Zatz
,
Sergio Rosenberg
,
M. Passos-Bueno
American Journal of Medical Genetics. Part A
2004
Corpus ID: 28424988
X-linked mental retardation (XLMR) is one of the most common human birth defects, occurring with an incidence of approximately 1…
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2000
2000
DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner.
Maurice P. Scheer
,
S. M. V. D. Maarel
,
+5 authors
H. Nothwang
Genomics
2000
Corpus ID: 922926
DXS6673E is a candidate gene for nonspecific X-linked mental retardation and encodes a novel Zn-finger protein. The ortholog…
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1999
1999
Cloning and mapping of members of the MYM family.
D. Smedley
,
R. Hamoudi
,
Y. Lu
,
C. Cooper
,
J. Shipley
Genomics
1999
Corpus ID: 40772268
Tandem repeats of a novel, putative, zinc-binding motif (MYM) have been described within the products of two, highly homologous…
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1997
1997
AFX1 and p54nrb: fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism
U. Peters
,
G. Haberhausen
,
M. Kostrzewa
,
D. Nolte
,
U. Müller
Human Genetics
1997
Corpus ID: 35332593
Abstract We have mapped AFX1 and p54nrb to a yeast artificial chromosome (YAC) contig of Xq13.1 that harbors the X-linked…
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