(Q37743327)

22 August 2017

1 reference

title

LMBRD1: the gene for the cblF defect of vitamin B₁₂ metabolism (English)

1 reference

methylmalonic aciduria and homocystinuria type cblF

22 August 2017

0 references

0 references

1 reference

1

Frank Rutsch

1 reference

22 August 2017

Susann Gailus

2

1 reference

22 August 2017

Terttu Suormala

series ordinal

3

1 reference

22 August 2017

Brian Fowler

series ordinal

4

1 reference

22 August 2017

publication date

6 May 2010

1 reference

Journal of Inherited Metabolic Disease

22 August 2017

published in

1 reference

22 August 2017

volume

34

1 reference

22 August 2017

issue

1

1 reference

22 August 2017

page(s)

121-126

1 reference

Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers

22 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Gene identification for the cblD defect of vitamin B12 metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Beta-lactoglobulin binds retinol and protoporphyrin IX at two different binding sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

The lipocalin protein family: structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Lipocalin-interacting-membrane-receptor (LIMR) mediates cellular internalization of beta-lactoglobulin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

The protein and the gene encoding the receptor for the cellular uptake of transcobalamin-bound cobalamin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Molecular physiology and pathophysiology of lysosomal membrane transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Lysosomal cobalamin accumulation in fibroblasts from a patient with an inborn error of cobalamin metabolism (cblF complementation group): visualization by electron microscope radioautography

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Novel nuclear export signal-interacting protein, NESI, critical for the assembly of hepatitis delta virus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Molecular cloning of a novel lipocalin-1 interacting human cell membrane receptor using phage display

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Antisense down-regulation of lipocalin-interacting membrane receptor expression inhibits cellular internalization of lipocalin-1 in human NT2 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Construction and characterization of a highly stable human:rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9083-9

Vitamin B12 transport by rat liver lysosomal membrane vesicles

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20446115

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[The enhancement of development at nursery school age].

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20446115

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10545-010-9083-9

1 reference

22 August 2017

1 reference