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PPP2R5B gene
Known as:
PP2A, B subunit, PR61 beta isoform
, PROTEIN PHOSPHATASE 2, REGULATORY SUBUNIT B (B56), BETA
, PR61B
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This gene plays a role in the negative control of cell growth and division.
National Institutes of Health
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Related topics
Related topics
9 relations
Cell Proliferation Regulatory Process
DNA Replication
Dephosphorylation
Hydrolysis
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
MiR‐8‐3p regulates hyperthermia‐induced lactate secretion by targeting PPP2R5B in boar Sertoli cells
Yu Hu
,
Jie Deng
,
+8 authors
Xian-Zhong Wang
Molecular Reproduction and Development
2019
Corpus ID: 201846025
Lactate produced by glycolysis in Sertoli cells (SCs) is the main energy substrate for developing germ cells and plays a vital…
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2018
2018
Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population
A. Mowat
,
Michael Crompton
,
+4 authors
S. Dawson
Human Genetics
2018
Corpus ID: 19171480
Otosclerosis is a common form of hearing loss which typically presents in young adults. The disease has a familial, monogenic…
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Highly Cited
2015
Highly Cited
2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth
C. Loveday
,
K. Tatton-Brown
,
+12 authors
N. Rahman
Human Molecular Genetics
2015
Corpus ID: 13902138
Overgrowth syndromes comprise a group of heterogeneous disorders characterised by excessive growth parameters, often in…
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2015
2015
Deletion of 11q12.3-11q13.1 in a patient with intellectual disability and childhood facial features resembling Cornelia de Lange syndrome.
M. I. Boyle
,
C. Jespersgaard
,
+4 authors
Z. Tümer
Gene
2015
Corpus ID: 27962232
2015
2015
Mutations in the PP 2 A regulatory subunit B family genes PPP 2 R 5 B , PPP 2 R 5 C and PPP 2 R 5 D cause human overgrowth
C. Loveday
,
K. Tatton-Brown
,
+12 authors
N. Rahman
2015
Corpus ID: 3527342
Overgrowth syndromes comprise a group of heterogeneous disorders characterised by excessive growth parameters, often in…
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2006
2006
Mutation analysis of five candidate genes in familial breast cancer
Anna J Marsh
,
S. Healey
,
+8 authors
kConFab
Breast Cancer Research and Treatment
2006
Corpus ID: 21030334
Most of the known breast cancer susceptibility genes (BRCA1, BRCA2, CHEK2 and ATM) are involved in the damage response pathway…
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Review
2004
Review
2004
The CD8 isoform CD8alphaalpha is not a functional homologue of the TCR co-receptor CD8alphabeta.
Denise Gangadharan
,
H. Cheroutre
Current Opinion in Immunology
2004
Corpus ID: 9982248
Although structurally similar, CD8alphabeta and CD8alphaalpha have notably diverted with regard to function. Whereas CD8alphabeta…
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2000
2000
Isolation and Characterization of par 1 1 and par 2 1 : Two Schizosaccharomyces pombe Genes Encoding B 9 Subunits of Protein Phosphatase 2 A
Wei Jiang
,
R. Hallberg
2000
Corpus ID: 38074152
Protein phosphatase 2A (PP2A) is one of the major serine/threonine phosphatases found in eukaryotic cells. We cloned two genes…
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Highly Cited
1997
Highly Cited
1997
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.
I. Lemmens
,
W. Ven
,
+28 authors
R. Thakker
Human Molecular Genetics
1997
Corpus ID: 27960293
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids…
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1997
1997
Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.
I. Lemmens
,
J. Merregaert
,
+22 authors
R. Thakker
Genomics
1997
Corpus ID: 25063906
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome characterized by parathyroid…
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