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SPTBN2 gene
Known as:
GTRAP41
, spectrin beta, non-erythrocytic 2
, SPTBN2
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This gene plays a role in actin filament function.
National Institutes of Health
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Related topics
Related topics
6 relations
Cell Movement
Cytokinesis
Muscle Contraction
Regulation of Cell Shape
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Han Chinese family with early‐onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene
Ting Huang
,
Chenyu Gao
,
+4 authors
Ying-Dong Zhang
Brain and Behavior
2019
Corpus ID: 199451431
To identify deletions, duplications, and point mutations in 55 previously reported genes associated with Parkinson's disease (PD…
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2015
2015
Attenuation of erythrocytic actylcholinesterase by antidepressants
S. Tariq
,
H. Khan
,
N. Muhammad
Toxicology and industrial health
2015
Corpus ID: 32986411
The current study was aimed to scrutinize acetylcholinesterase (AchE) inhibitory profile of two antidepressants, diazepam and…
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Review
2013
Review
2013
Aspirin-Intolerant Asthma: A Comprehensive Review of Biomarkers and Pathophysiology
J. Velazquez
,
L. Teran
Clinical reviews in allergy and immunology
2013
Corpus ID: 37575242
Aspirin-exacerbated respiratory disease is a tetrad of nasal polyps, chronic hypertrophic eosinophilic sinusitis, asthma, and…
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2011
2011
Erythrocytic or serum hydrogen sulfide association with hypertension development in untreated essential hypertension.
Mei Zheng
,
Q. Zeng
,
+4 authors
B. Geng
Chinese Medical Journal
2011
Corpus ID: 32933011
BACKGROUND Endogenous hydrogen sulfide (H(2)S) plays an important role in hypertension. The aim of this study was to investigate…
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2010
2010
Molecular genetic analysis of a new form of spinocerebellar ataxia in a Chinese Han family
Yuan Yuan
,
Xin Zhou
,
Feng-ming Ding
,
Yumin Liu
,
Jian-cheng Tu
Neuroscience Letters
2010
Corpus ID: 32412378
2007
2007
Screening of the SPTBN2 (SCA5) gene in German SCA patients
C. Zühlke
,
V. Bernard
,
+4 authors
K. Bürk
Journal of Neurology
2007
Corpus ID: 23753717
AbstractThe spinocerebellar ataxias (SCAs) with autosomal dominant inheritance are a clinically and genetically heterogeneous…
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1989
1989
[Hematologic significance of erythrocytic macrocytosis: prospective analysis of 109 successively studied cases].
J. J. Outeiriño Pérez
,
J. Sánchez Fayos
,
+6 authors
J. S. Sánchez Martín
Sangre
1989
Corpus ID: 31889324
The aim of the present work was to perform a prospective analysis of the significance of macrocytic red cells through the study…
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1989
1989
[HLA antigen frequencies in patients with autosomal dominant polycystic kidney degeneration].
J. Spengler
,
S. Wegener
,
H. Schüler
,
G. Kraatz
Zeitschrift fur Urologie und Nephrologie
1989
Corpus ID: 42281875
20 non-related patients suffering from autosomal dominantly polycystic renal disease were HLA-A, -B, -C and -DR typified and the…
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1983
1983
Protective Plasmodium knowlesi Mr 74,000 antigen in membranes of schizont-infected rhesus erythrocytes
R. Schmidt‐Ullrich
,
J. Lightholder
,
M. T. Monroe
Journal of Experimental Medicine
1983
Corpus ID: 12442430
The immunogenic Plasmodium knowlesi (H strain) Mr 74,000 protein in membranes of schizont-infected rhesus erythrocytes was…
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1982
1982
Genetic control of the quantitative variation of erythrocytic glyoxalase-1 (GLO-1) in mice
P. Rubinstein
,
K. Vienne
Biochemical Genetics
1982
Corpus ID: 27809194
Quantitative genetic variation in the glyoxalase-1 content (QGlo-1) of red cells of mice is described. Its genetic control is…
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