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BRSK1 gene

Known as: BR serine/threonine kinase 1, BRSK1, KIAA1811 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Genetic variants of age at menopause are not related to timing of ovarian failure in breast cancer survivors
Objective: To determine if interindividual genetic variation in single-nucleotide polymorphisms (SNPs) related to age at natural… 
2017
2017
Protein kinase KIN10 from Arabidopsis thaliana as a potential regulator of primary microtubule nucleation centers in plants
The nearest plant homologues of animal protein kinase BRSK were identified using the methods of classical and structural… 
2014
2014
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women.
2014
2014
Quantitative-Proteomic Comparison of Alpha and Beta Cells to Uncover Novel Targets for Lineage Reprogramming
Type-1 diabetes (T1D) is an autoimmune disease in which insulin-secreting pancreatic beta cells are destroyed by the immune… 
2013
2013
Evaluating GWAS-Identified SNPs for Age at Natural Menopause among Chinese Women
Background Age at natural menopause (ANM) is a complex trait with high heritability and is associated with several major hormonal… 
2013
2013
BRSK1 regulates glucose uptake in L6 cells and mouse skeletal muscle
2013
2013
Development of overweight and obesity in mid-age women from the Australian Longitudinal on Women Health Study
2013
2013
Regulació de la Brain-specific Kinase 1 (BRSK1) neuronal per sulfàtid i modificacions post-traduccionals
Les Brain Specific Kinase 1 i 2 (BRSK1 i 2), tambe conegudes com a SAD quinases, son proteines Ser/Thr quinases de la familia de… 
2008
2008
Investigating the regulation of brain specific kinases 1 and 2.
2004
2004
Mapping of a translocation breakpoint in a Peutz–Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11‐negative PJS cases
Germ‐line mutations in the serine‐threonine kinase gene STK11 (LKB1) cause Peutz–Jeghers syndrome (PJS), a rare autosomal… 
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