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RBM10 gene
Known as:
RNA binding motif protein 10
, DXS8237E
, RNA-BINDING MOTIF PROTEIN 10
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This gene is involved in RNA binding and processing.
National Institutes of Health
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Related topics
Related topics
6 relations
Ligand Binding
RBM10 protein, human
RBM11 gene
RBM22 gene
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
A Splicing-Independent Function of RBM10 Controls Specific 3' UTR Processing to Regulate Cardiac Hypertrophy.
Nimmy Mohan
,
Vikas Kumar
,
Divya T. Kandala
,
C. Kartha
,
Rakesh S. Laishram
Cell Reports
2018
Corpus ID: 52844024
Highly Cited
2017
Highly Cited
2017
Functional analysis reveals that RBM10 mutations contribute to lung adenocarcinoma pathogenesis by deregulating splicing
Jiawei Zhao
,
Yue Sun
,
+8 authors
Yongbo Wang
Scientific Reports
2017
Corpus ID: 8816435
RBM10 is an RNA splicing regulator that is frequently mutated in lung adenocarcinoma (LUAD) and has recently been proposed to be…
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Highly Cited
2016
Highly Cited
2016
Tumor suppressor properties of the splicing regulatory factor RBM10
Jordi Hernández
,
Elias Bechara
,
Doerte Schlesinger
,
J. Delgado
,
L. Serrano
,
J. Valcárcel
RNA Biology
2016
Corpus ID: 41526
ABSTRACT RBM10 is an RNA binding protein and alternative splicing regulator frequently mutated in lung adenocarcinomas. Recent…
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Highly Cited
2014
Highly Cited
2014
RBM10 regulates alternative splicing
A. Inoue
,
N. Yamamoto
,
M. Kimura
,
K. Nishio
,
Hideo Yamane
,
K. Nakajima
FEBS Letters
2014
Corpus ID: 10303057
Highly Cited
2013
Highly Cited
2013
Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation
Yongbo Wang
,
A. Gogol-Döring
,
+12 authors
Wei Chen
EMBO Molecular Medicine
2013
Corpus ID: 7346399
RBM10 encodes an RNA binding protein. Mutations in RBM10 are known to cause multiple congenital anomaly syndrome in male humans…
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Highly Cited
2011
Highly Cited
2011
Characterization of a family of RanBP2-type zinc fingers that can recognize single-stranded RNA.
Cuong D Nguyen
,
R. E. Mansfield
,
+4 authors
J. Mackay
Journal of Molecular Biology
2011
Corpus ID: 15907015
Highly Cited
2011
Highly Cited
2011
Long‐term survival in TARP syndrome and confirmation of RBM10 as the disease‐causing gene
K. Gripp
,
E. Hopkins
,
J. Johnston
,
Caitlin Krause
,
W. Dobyns
,
L. Biesecker
American Journal of Medical Genetics. Part A
2011
Corpus ID: 25250437
TARP syndrome, comprising Talipes equinovarus, atrial septal defect (ASD), Robin sequence (micrognathia, glossoptosis, and cleft…
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2008
2008
S1‐1 nuclear domains: characterization and dynamics as a function of transcriptional activity
A. Inoue
,
K. Tsugawa
,
+9 authors
T. Tani
Biology of the Cell
2008
Corpus ID: 9893063
Background information. The RNA‐binding protein S1‐1, also called RBM10 (RNA‐binding motif 10), is a paralogue of putative tumour…
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Highly Cited
2006
Highly Cited
2006
Positive correlation between the expression of X‐chromosome RBM genes (RBMX, RBM3, RBM10) and the proapoptotic Bax gene in human breast cancer
F. Martínez‐Arribas
,
D. Agudo
,
+4 authors
J. Schneider
Journal of Cellular Biochemistry
2006
Corpus ID: 9804734
In a recent report, it has been postulated that the ubiquitous RBM proteins might constitute a novel family of apoptosis…
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Highly Cited
2002
Highly Cited
2002
An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders.
D. Thiselton
,
J. McDowall
,
+6 authors
A. Meindl
Genomics
2002
Corpus ID: 38331953
Human chromosome Xp11.3-Xp11.23 encompasses the map location for a growing number of diseases with a genetic basis or genetic…
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