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RRM2B gene
Known as:
RRM2B
, Ribonucleotide Reductase M2 B (TP53 Inducible) Gene
, RIBONUCLEOTIDE REDUCTASE SMALL SUBUNIT 2-LIKE, p53-INDUCIBLE
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This gene plays a role in deoxyribonucleoside diphosphate metabolism.
National Institutes of Health
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Related topics
Related topics
5 relations
Cell Proliferation
DNA Replication
Oxidation-Reduction
Ribonucleoside-Diphosphate Reductase Subunit M2 B
Narrower (1)
RRM2B wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B
L. Roberts
,
S. Julius
,
+13 authors
R. Ramesar
Human Mutation
2020
Corpus ID: 221239656
More than two decades ago, a recessive syndromic phenotype affecting kidneys, eyes, and ears, was first described in the…
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2019
2019
External ophthalmoplegia requires genetic work-up prior to strabismus surgery
J. Finsterer
2019
Corpus ID: 212522827
The main shortcoming of the study is that the cause of CPEO was not provided, neither for patient-1, a 26 year male nor for…
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Review
2017
Review
2017
Phenotypic and Genotypic Heterogeneity of RRM 2 B Variants Finsterer
J. Finsterer
,
S. Zarrouk-Mahjoub
2017
Corpus ID: 260575975
Autosomaldominant (AD)orautosomalrecessive(AR)mutations in the RRM2B gene cause a mitochondrial multiorgan disorder syndrome…
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2017
2017
Effects of distinct drugs on gene transcription in an osteosarcoma cell line
Hui Zhou
,
X. Cui
,
Hongping Yuan
,
Boyin Zhang
,
Chun-yang Meng
,
Dongxu Zhao
Oncology Letters
2017
Corpus ID: 9671047
Osteosarcoma (OS) is a common cancerous bone tumor which has a detrimental impact on the lives of patients and their families…
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2017
2017
Microarray expression analysis of MYCN-amplified neuroblastoma cells after inhibition of CDK2.
H. Song
,
F. Wu
,
+4 authors
C. Lin
Neoplasma (Bratislava)
2017
Corpus ID: 30588335
The study aimed to explore the underlying molecular mechanisms of CDK2 inhibition in neuroblastoma by bioinformatics analysis…
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2012
2012
Adults with RRM 2 B-related mitochondrial disease have distinct clinical and molecular characteristics
R. Pitceathly
,
Conrad Smith
,
+24 authors
G. Gorman
2012
Corpus ID: 84837668
Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics Robert D. S. Pitceathly…
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2012
2012
The c.48G > A variant in the mitochondrial DNA maintenance gene, RRM2B, causes adult-onset autosomal dominant PEO via aberrant splicing
C. Smith
,
Julie C. Evans
,
+9 authors
C. Fratter
2012
Corpus ID: 89522573
2011
2011
Abstract 4183: Ribonucleotide reductase small subunit M2B associates with better survival of colorectal cancers through inhibiting tumor invasion and metastasis
Xiyong Liu
,
Xiaochen Wang
,
+16 authors
Y. Yen
2011
Corpus ID: 70661520
Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL Previous studies have demonstrated that RRM2B…
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2010
2010
Deleterious mutations in RRM2B, a gene responsible for maintenance of mtDNA, result in severe reduction of mtDNA content in skeletal muscle
R. Coster
,
J. Smet
,
B. Paepe
,
W. Lissens
,
L. Meirleir
,
S. Seneca
2010
Corpus ID: 86949234
Mutations in POLG1, DGUOK, TK2, SUCLG1, SUCLA2, PEO1, MPV17 and TYMP can cause mtDNA depletion. Recently, deleterious mutations…
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Review
1997
Review
1997
Use and Misuse of QCD Sum Rules in Heavy-to-light Transitions : the Decay B → ρeν Reexamined
P. Ball
,
V. Braun
1997
Corpus ID: 15919446
The existing calculations of the form factors describing the decay B → ρeν from QCD sum rules have yielded conflicting results at…
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