(Q38356758)

2 September 2017

Glycerol metabolism and the determination of triglycerides--clinical, biochemical and molecular findings in six subjects (English)

1 reference

2 September 2017

1 reference

Christina Hellerud

1

1 reference

2 September 2017

Alberto Burlina

2

1 reference

2 September 2017

Carlo Gabelli

3

1 reference

2 September 2017

James R Ellis

4

1 reference

2 September 2017

Per-Georg Nyholm

5

1 reference

2 September 2017

Sven Lindstedt

6

1 reference

2 September 2017

1 January 2003

1 reference

Clinical Chemistry and Laboratory Medicine

2 September 2017

1 reference

2 September 2017

41

1 reference

2 September 2017

1

1 reference

2 September 2017

46-55

1 reference

Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III)

2 September 2017

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

The binding of glycerol kinase to the outer membrane of rat liver mitochondria: Its importance in metabolic regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Structural organization and mapping of the human mitochondrial glycerol phosphate dehydrogenase-encoding gene and pseudogene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Human glycerol kinase deficiency: An inborn error of compartmental metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Isolated and contiguous glycerol kinase gene disorders: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Glycerol kinase deficiency: evidence for complexity in a single gene disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Familial hyperglycerolemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Concordance of X-linked glycerol kinase deficiency with X-linked congenital adrenal hypoplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Complex glycerol kinase deficiency: molecular-genetic, cytogenetic, and clinical studies of five Japanese patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

The glycerol kinase gene family: structure of the Xp gene, and related intronless retroposons

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Clinical and biochemical observations on three cases of fructose-1,6-diphosphatase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Sites of inhibition of mitochondrial electron transport in macrophage-injured neoplastic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Isolation of the human Xp21 glycerol kinase gene by positional cloning

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Glycerol as a correlate of impaired glucose tolerance: dissection of a complex system by use of a simple genetic trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Nomenclature for the description of human sequence variations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Structure of the regulatory complex of Escherichia coli IIIGlc with glycerol kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Glycerol kinase from Escherichia coli and an Ala65-->Thr mutant: the crystal structures reveal conformational changes with implications for allosteric regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Information content of individual genetic sequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Sequence walkers: a graphical method to display how binding proteins interact with DNA or RNA sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Glyceroluria in healthy adults, mentally ill adults and children selected for metabolic screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GIS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.009

21 January 2018

Identifiers

DOI

10.1515/CCLM.2003.009

1 reference

2 September 2017

1 reference