UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 152

Sortiert nach

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

Nature genetics, 2012-10, Vol.44 (10), p.1152-1155

2012

Volltextzugriff (PDF)

Staphylococcus aureus CcpA Affects Virulence Determinant Production and Antibiotic Resistance

Antimicrobial Agents and Chemotherapy, 2006-04, Vol.50 (4), p.1183-1194

2006

Volltextzugriff (PDF)

3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals

Orphanet journal of rare diseases, 2012-05, Vol.7 (1), p.31-31, Article 31

2012

Volltextzugriff (PDF)

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

Nature genetics, 2009-02, Vol.41 (2), p.234-239

2009

Volltextzugriff (PDF)

Secondary NAD+ deficiency in the inherited defect of glutamine synthetase

Journal of inherited metabolic disease, 2015-11, Vol.38 (6), p.1075-1083

2015

Volltextzugriff (PDF)

Cryptic Exon Activation by Disruption of Exon Splice Enhancer

The Journal of biological chemistry, 2009-10, Vol.284 (42), p.28953-28957

2009

Volltextzugriff (PDF)

Virus Safety of Intravenous Immunoglobulin: Future Challenges

Clinical reviews in allergy & immunology, 2005, Vol.29 (3), p.333-344

2005

Volltextzugriff (PDF)

Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism

Human molecular genetics, 2012-03, Vol.21 (6), p.1410-1418

2012

Volltextzugriff (PDF)

Gene Identification for the cblD Defect of Vitamin B 12 Metabolism

The New England journal of medicine, 2008-04, Vol.358 (14), p.1454-1464

2008

Volltextzugriff (PDF)

Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations

Human mutation, 2009-07, Vol.30 (7), p.1072-1081

2009

Volltextzugriff (PDF)

Gene Identification for the cblD Defect of Vitamin B12 Metabolism

The New England journal of medicine, 2008-04, Vol.358 (14), p.1454-1464

2008

Volltextzugriff (PDF)

Verification of effective Zika virus reduction by production steps used in the manufacture of plasma‐derived medicinal products

Transfusion (Philadelphia, Pa.), 2017-03, Vol.57 (3), p.720-721

2017

Volltextzugriff (PDF)

Alignment Process for Glass Substrates Using Electrostatic Self-Assembly

Production at the Leading Edge of Technology, p.448-456

Volltextzugriff (PDF)

Secondary NAD^sup +^ deficiency in the inherited defect of glutamine synthetase

Journal of inherited metabolic disease, 2015-11, Vol.38 (6), p.1075

2015

Volltextzugriff (PDF)

Cryptic Exon Activation by Disruption of Exon Splice Enhancer: NOVEL MECHANISM CAUSING 3-METHYLCROTONYL-CoA CARBOXYLASE DEFICIENCY

The Journal of biological chemistry, 2009-10, Vol.284 (42), p.28953-28957

2009

Volltextzugriff (PDF)

Pathogen inactivation and removal procedures used in the production of intravenous immunoglobulins

Biologicals, 2007-03, Vol.35 (1), p.35-42

2007

Volltextzugriff (PDF)

Mutations in ABCD4 cause a new inborn error of vitamin [B.sub.12] metabolism

Nature genetics, 2012-10, Vol.44 (10), p.1152

2012

Volltextzugriff (PDF)

Characterisation of a chromatographically produced anti-D immunoglobulin product

Journal of chromatography. B, Biomedical sciences and applications, 1997-10, Vol.700 (1), p.241-248

1997

Volltextzugriff (PDF)

A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient

Journal of inherited metabolic disease, 2010-02, Vol.33 (1), p.17-24

2010

Volltextzugriff (PDF)

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

Journal of inherited metabolic disease, 2010-02, Vol.33 (1), p.17-24

2010

Volltextzugriff (PDF)

Mutations in ABCD4 cause a new inborn error of vitamin B sub(12) metabolism

Nature genetics, 2012-10, Vol.44 (10), p.1152-1155

2012

Volltextzugriff (PDF)

Mutations in ABCD4 cause a new inborn error of vitamin B^sub 12^ metabolism

Nature genetics, 2012-10, Vol.44 (10), p.1152

2012

Volltextzugriff (PDF)

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin [B.sub.12] metabolism

Nature genetics, 2009-02, Vol.41 (2), p.234

2009

Volltextzugriff (PDF)

Spectrum of mutations in MMACHC , allelic expression, and evidence for genotypeâphenotype correlations

Human mutation, 2009-07, Vol.30 (7), p.1072-1081

2009

Volltextzugriff (PDF)

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B 12 metabolism

Nature genetics, 2009-02, Vol.41 (2), p.234-239

2009

Volltextzugriff (PDF)

1 – 25 von 152

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(135)
Mit Volltextzugriff
(137)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

Staphylococcus aureus CcpA Affects Virulence Determinant Production and Antibiotic Resistance

3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals

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

Secondary NAD+ deficiency in the inherited defect of glutamine synthetase

Cryptic Exon Activation by Disruption of Exon Splice Enhancer

Virus Safety of Intravenous Immunoglobulin: Future Challenges

Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism

Gene Identification for the cblD Defect of Vitamin B 12 Metabolism

Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations

Gene Identification for the cblD Defect of Vitamin B12 Metabolism

Verification of effective Zika virus reduction by production steps used in the manufacture of plasma‐derived medicinal products

Alignment Process for Glass Substrates Using Electrostatic Self-Assembly

Secondary NAD^sup +^ deficiency in the inherited defect of glutamine synthetase

Cryptic Exon Activation by Disruption of Exon Splice Enhancer: NOVEL MECHANISM CAUSING 3-METHYLCROTONYL-CoA CARBOXYLASE DEFICIENCY

Pathogen inactivation and removal procedures used in the production of intravenous immunoglobulins

Mutations in ABCD4 cause a new inborn error of vitamin [B.sub.12] metabolism

Characterisation of a chromatographically produced anti-D immunoglobulin product

A novel mutation in LMBRD1 causes the cblF defect of vitamin B12 metabolism in a Turkish patient

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

Mutations in ABCD4 cause a new inborn error of vitamin B sub(12) metabolism

Mutations in ABCD4 cause a new inborn error of vitamin B^sub 12^ metabolism

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin [B.sub.12] metabolism

Spectrum of mutations in MMACHC , allelic expression, and evidence for genotypeâphenotype correlations

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B 12 metabolism

Suchergebnisse filtern