Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
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Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretionIndividualized therapy for type 2 diabetes: clinical implications of pharmacogenetic data.What have we learnt from genetic studies of type 2 diabetes in Chinese?Lack of association between genetic polymorphisms within DUSP12 - ATF6 locus and glucose metabolism related traits in a Chinese populationA variation in NOS1AP gene is associated with repaglinide efficacy on insulin resistance in type 2 diabetes of Chinese.A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes.Genetic variations in APPL2 are associated with overweight and obesity in a Chinese population with normal glucose tolerance.CPVL/CHN2 genetic variant is associated with diabetic retinopathy in Chinese type 2 diabetic patients.An interaction between a FNDC5 variant and obesity modulates glucose metabolism in a Chinese Han population.Serum Proteome Changes in Healthy Subjects with Different Genotypes of NOS1AP in the Chinese PopulationDiabetes, lower extremity amputation, loss of protective sensation, and neuronal nitric oxide synthase associated protein in the chronic renal insufficiency cohort studyLow Expression of CAPON in Glioma Contributes to Cell Proliferation via the Akt Signaling PathwayAssociation of type 2 diabetes susceptibility loci with peripheral nerve function in a Chinese population with diabetes.Lack of association between TLR4 genetic polymorphisms and diabetic nephropathy in a Chinese population.Genetic advances of type 2 diabetes in Chinese populations.Pharmacogenomics of glinides.The role of Capon in multiple myeloma.NOS1AP genetic variation is associated with impaired healing of diabetic foot ulcers and diminished response to healing of circulating stem/progenitor cells.Common variants in or near ZNRF1, COLEC12, SCYL1BP1 and API5 are associated with diabetic retinopathy in Chinese patients with type 2 diabetes.Association of genetic variants of BMP4 with type 2 diabetes mellitus and clinical traits in a Chinese Han population.Association of Toll-like Receptor 4 Gene polymorphisms with susceptibility to type 2 diabetes mellitus in the Chinese population.Effects of NOS1AP rs12742393 polymorphism on repaglinide response in Chinese patients with type 2 diabetes mellitus.Neutrophil microparticle production and inflammasome activation by hyperglycemia due to cytoskeletal instability.Genetic variants of LPIN1 indicate an association with Type 2 diabetes mellitus in a Chinese population.Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population
P2860
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P2860
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@en
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@nl
type
label
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@en
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@nl
prefLabel
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@en
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@nl
P2093
P1433
P1476
Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
@en
P2093
P2888
P304
P356
10.1007/S00125-009-1594-2
P577
2009-11-24T00:00:00Z