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PPP1R3A gene
Known as:
PPP1R3
, PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 3
, GM
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Targeted next generation sequencing of well-differentiated/dedifferentiated liposarcoma reveals novel gene amplifications and mutations
N. Somaiah
,
Hannah C. Beird
,
+13 authors
D. Hong
OncoTarget
2018
Corpus ID: 13663328
Well-differentiated/dedifferentiated liposarcoma is a common soft tissue sarcoma with approximately 1500 new cases per year…
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2018
2018
Role of protein phosphatase 1 glycogen-associated regulatory subunit in asthma
Mayra D. Álvarez-Santos
,
Marisol Álvarez-González
,
+5 authors
B. Bazán-Perkins
Airway Cell Biology and Immunopathology
2018
Corpus ID: 81784158
Muscle-specific glycogen-targeting subunit (PPP1R3A) of protein phosphatase 1 is involved in muscle glycogen regulation…
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2017
2017
SDRP Journal of Infectious Diseases Treatement & Therapy
K. Isobe
,
N. Nishio
,
T. Hasegawa
2017
Corpus ID: 54507503
Obesity-derived metabolic syndrome is one of the most important medical problems in the world. Recently, we have developed murine…
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2016
2016
Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.
M. Prabhanjan
,
Raviraj V. Suresh
,
Megha N. Murthy
,
N. Ramachandra
Diabetes Research and Clinical Practice
2016
Corpus ID: 12206507
2016
2016
Murine model of obesity-induced type II diabetes by GADD34 (PPP1R15A) and other phosphatase 1 regulatory subunits deficiency.
K. Isobe
,
N. Nishio
,
T. Hasegawa
,
Sift Desk Journals Open Access Journals
2016
Corpus ID: 90935255
Obesity-derived metabolic syndrome is one of the most important medical problems in the world. Recently, we have developed murine…
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2016
2016
Abstract 17054: Genes Associated With Inotrope Requirements in Children Undergoing Tetralogy of Fallot Repair
Stephen Lee
,
A. Manickaraj
,
+5 authors
S. Mital
2016
Corpus ID: 80232091
Introduction: Inotropes are used to prevent or treat postoperative low cardiac output syndrome. Common variants in adrenergic…
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2011
2011
Phenotype of Foxp2 Haploinsufficiency in a Mother and Son Materials and Methods Array Comparative Genomic Hybridization (acgh)
Gregory M Rice
,
G. Raca
,
+11 authors
Laffin Jj
2011
Corpus ID: 263450849
Disruptions in FOXP2, a transcription factor, are the only known monogenic cause of speech and language impairment. We report on…
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2007
2007
Obesity modifies the effects of the Asp905Tyr variant of PPP1R3A on risk of type 2 diabetes and insulin sensitivity
S. Mammarella
,
B. Creati
,
+15 authors
A. Cama
Diabetes, obesity and metabolism
2007
Corpus ID: 8758819
Interactions between genetic and environmental factors cause insulin resistance leading to type2diabetesmellitus. Three frequent…
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2000
2000
Alterations of the PPP1R3 gene in hematological malignancies.
K. Inoue
,
T. Kohno
,
+5 authors
J. Yokota
International Journal of Oncology
2000
Corpus ID: 19288090
PPP1R3 (protein phosphatase 1, regulatory subunit 3) is a candidate tumor suppressor gene at chromosome 7q31, since nonsense and…
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