Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evaluation of Sox2 genetic effect on the development of type 2 diabetes.

Gene - 15 Oct 2011

Gu Harvest F, Gu Tianwei, Ostenson Claes-Göran, Kärvestedt Lars, Brismar Kerstin

Abstract excerpt

Sox2 is a transcription factor, which plays an important role in the induction of pluripotent stem cells from somatic cells. The Sox2 gene is located in chromosome 3q26.33 and resides in a linkage region of diabetes. In the present study, we attempted to evaluate the genetic effect of Sox2 in the development of type 2 diabetes (T2D). A total of 1598 Swedish subjects of T2D, pre-diabetes and non-diabetic control...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Diabetes Mellitus, Type 2
Share to Gene Expression

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Islets of Langerhans

Share to Polymorphism, Single Nucleotide

Share to RNA, Messenger

Share to SOXB1 Transcription Factors

Source

Identifiers

PMID: 21803132
DOI: 10.1016/j.gene.2011.07.014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Evaluation of Sox2 genetic effect on the development of type 2 diabetes.PMID 21803132Read ↗

SOX2 has gender-specific genetic effects on diabetic nephropathy in samples from patients with type 1 diabetes mellitus in the GoKinD study.Semantic proximity Read ↗

Linkage studies of SOX13, the ICA12 autoantigen gene, in families with type 1 diabetes.Semantic proximity Read ↗

Quantitative assessment of the influence of hematopoietically expressed homeobox variant (rs1111875) on type 2 diabetes risk.Semantic proximity Read ↗

Genetic Approaches to the Study of Gene Variants and Their Impact on the Pathophysiology of Type 2 Diabetes.Semantic proximity Read ↗

Genetics of Type 2 Diabetes—Pitfalls and PossibilitiesSemantic proximity Read ↗

Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study.Semantic proximity Read ↗

PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population.Semantic proximity Read ↗

Genetics of type 2 diabetes: insights into the pathogenesis and its clinical application.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.