Adipose transplant for inborn errors of branched chain amino acid metabolism in mice. - Wikidata - wikimedia - TriplyDB

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

http://www.wikidata.org/entity/Q37640465

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The Emerging Role of Branched-Chain Amino Acids in Insulin Resistance and Metabolism Branched-chain amino acids in metabolic signalling and insulin resistance Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders.Global deletion of BCATm increases expression of skeletal muscle genes associated with protein turnover Branched-chain amino acid catabolism fuels adipocyte differentiation and lipogenesis Alloisoleucine differentiates the branched-chain aminoacidemia of Zucker and dietary obese rats Osteocalcin immunohistochemical expression during repair of critical-sized bone defects treated with subcutaneous adipose tissue in rat and rabbit animal model.Alterations of plasma metabolite profiles related to adipose tissue distribution and cardiometabolic risk.

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Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

http://www.wikidata.org/entity/Q37640465

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 30 May 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@en

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@nl

type

label

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@en

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@nl

prefLabel

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@en

Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@nl

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J.YMGME.2013.05.010

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Molecular Genetics and Metabolism

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Adipose transplant for inborn errors of branched chain amino acid metabolism in mice.

@en

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Christopher J Lynch

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Gang Chen

http://www.w3.org/2001/XMLSchema#string

Heather A Zimmerman

http://www.w3.org/2001/XMLSchema#string

Kristine C Olson

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P2860

A novel mitochondrial matrix serine/threonine protein phosphatase regulates the mitochondria permeability transition pore and is essential for cellular survival and development

Identification of a novel PP2C-type mitochondrial phosphatase

Regulation of branched-chain alpha-ketoacid dehydrogenase complex by covalent modification

Twist-1 is a PPARdelta-inducible, negative-feedback regulator of PGC-1alpha in brown fat metabolism

Disruption of BCATm in mice leads to increased energy expenditure associated with the activation of a futile protein turnover cycle

ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease

Improved glucose tolerance in mice receiving intraperitoneal transplantation of normal fat tissue.

Disruption of BCAA metabolism in mice impairs exercise metabolism and endurance.

Liver transplantation in maple syrup urine disease.

Adipose tissue branched chain amino acid (BCAA) metabolism modulates circulating BCAA levels.

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345-353

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scholarly article

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10.1016/J.YMGME.2013.05.010

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4

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109

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2013-05-30T00:00:00Z

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242016634

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23800641

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3955948

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