A truncation mutation in TBC1D4 in a family with acanthosis nigricans and postprandial hyperinsulinemia. (Q37224233)

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29 January 2020

title

A truncation mutation in TBC1D4 in a family with acanthosis nigricans and postprandial hyperinsulinemia (English)

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Justin Rochford

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Giles See How Yeo

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Claudia Langenberg

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Katherine Fawcett

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Inês Barroso

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Stephen O'Rahilly

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David B Savage

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Nicolas J Wareham

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author name string

Satya Dash

1

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Hiroyuki Sano

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Caroline S S Hyden

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Maria A Soos

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James Clark

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Andrew Rodin

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Celine Druet

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Y C Loraine Tung

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Gustav E Lienhard

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language of work or name

English

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publication date

22 May 2009

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Proceedings of the National Academy of Sciences of the United States of America

29 January 2020

published in

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volume

106

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issue

23

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page(s)

9350-9355

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Potential role of TBC1D4 in enhanced post-exercise insulin action in human skeletal muscle.

29 January 2020

cites work

1 reference

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6 September 2017

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New gene variants alter type 2 diabetes risk predominantly through reduced beta-cell function

6 September 2017

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IRS1-independent defects define major nodes of insulin resistance

6 September 2017

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Rapid activation of Akt2 is sufficient to stimulate GLUT4 translocation in 3T3-L1 adipocytes

6 September 2017

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TCF7L2 polymorphisms modulate proinsulin levels and beta-cell function in a British Europid population

6 September 2017

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Rab10, a target of the AS160 Rab GAP, is required for insulin-stimulated translocation of GLUT4 to the adipocyte plasma membrane

6 September 2017

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The GLUT4 glucose transporter

6 September 2017

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Contributions of beta-cell dysfunction and insulin resistance to the pathogenesis of impaired glucose tolerance and impaired fasting glucose

6 September 2017

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6 September 2017

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Unraveling the cellular mechanism of insulin resistance in humans: new insights from magnetic resonance spectroscopy

20 October 2018

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A family with severe insulin resistance and diabetes due to a mutation in AKT2.

6 September 2017

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Tissue-specific ablation of the GLUT4 glucose transporter or the insulin receptor challenges assumptions about insulin action and glucose homeostasis

6 September 2017

1 reference

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Insulin-stimulated phosphorylation of a Rab GTPase-activating protein regulates GLUT4 translocation

6 September 2017

1 reference

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A method to identify serine kinase substrates. Akt phosphorylates a novel adipocyte protein with a Rab GTPase-activating protein (GAP) domain

6 September 2017

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Glucose transporters and insulin action--implications for insulin resistance and diabetes mellitus

6 September 2017

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Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

6 September 2017

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Translational termination efficiency in mammals is influenced by the base following the stop codon.

6 September 2017

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Full intracellular retention of GLUT4 requires AS160 Rab GTPase activating protein

6 September 2017

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Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment.

26 June 2018

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Insulin resistance of puberty: a defect restricted to peripheral glucose metabolism.

26 June 2018

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Elevated plasma adiponectin in humans with genetically defective insulin receptors

26 June 2018

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Genetic factors in type 2 diabetes: the end of the beginning?

3 September 2018

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Mutant insulin receptors in syndromes of insulin resistance

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19470471

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Insulin resistance and the metabolic syndrome in obese French children

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19470471

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0900909106

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29 January 2020

0 references

1 reference

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29 January 2020

PubMed publication ID

19470471

1 reference