UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 166

Sortiert nach

Agm1/Pgm3-Mediated Sugar Nucleotide Synthesis Is Essential for Hematopoiesis and Development

Molecular and Cellular Biology, 2007-08, Vol.27 (16), p.5849-5859

2007

Link zum Volltext

Verfügbarkeit prüfen

A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)

The Journal of clinical investigation, 2001-12, Vol.108 (11), p.1613-1619

2001

Link zum Volltext

Verfügbarkeit prüfen

Hypoglycosylation due to dolichol metabolism defects

Biochimica et biophysica acta, 2009-09, Vol.1792 (9), p.888-895

2009

Link zum Volltext

Verfügbarkeit prüfen

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

Current protocols in molecular biology (Print), 2010-01, Vol.89 (1), p.17.13A.1-17.13A.25

2010

Link zum Volltext

Verfügbarkeit prüfen

cycloSaligenyl-mannose-1-monophosphates as a New Strategy in CDG-Ia Therapy: Hydrolysis, Mechanistic Insights and Biological Activity

European journal of organic chemistry, 2004-03, Vol.2004 (6), p.1228-1235

2004

Link zum Volltext

Verfügbarkeit prüfen

Evolution on SoC Integration : GSM Baseband-Radio in 0.13 μm CMOS Extended by Fully Integrated Power Management Unit

IEEE journal of solid-state circuits, 2008, Vol.43 (1), p.236-245

2008

Link zum Volltext

Verfügbarkeit prüfen

A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy

American journal of human genetics, 2007-03, Vol.80 (3), p.433-440

2007

Link zum Volltext

Verfügbarkeit prüfen

COG8 deficiency causes new congenital disorder of glycosylation type IIh

Human molecular genetics, 2007-04, Vol.16 (7), p.731-741

2007

Link zum Volltext

Verfügbarkeit prüfen

A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS

Human mutation, 2006-06, Vol.27 (6), p.524-531

2006

Link zum Volltext

Verfügbarkeit prüfen

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

Current Protocols in Protein Science, 2010-11, Vol.62 (1), p.12.4.1-12.4.25

2010

Link zum Volltext

Verfügbarkeit prüfen

Congenital Disorder of Glycosylation Type Ik (CDG-Ik): A Defect of Mannosyltransferase I

American journal of human genetics, 2004-03, Vol.74 (3), p.545-551

2004

Link zum Volltext

Verfügbarkeit prüfen

Expanding spectrum of congenital disorder of glycosylation Ig (CDG‐Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality

American journal of medical genetics. Part A, 2007-06, Vol.143A (12), p.1371-1378

2007

Link zum Volltext

Verfügbarkeit prüfen

An activated 5′ cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id)

Human mutation, 2004-05, Vol.23 (5), p.477-486

2004

Link zum Volltext

Verfügbarkeit prüfen

Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS)

Glycoconjugate journal, 2008-05, Vol.25 (4), p.375-382

2008

Link zum Volltext

Verfügbarkeit prüfen

Congenital disorder of glycosylation type Id : Clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins

Pediatric research, 2005-08, Vol.58 (2), p.248-253

2005

Link zum Volltext

Verfügbarkeit prüfen

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

Current Protocols in Immunology, 2010-04, Vol.89 (1), p.8.15.1-8.15.25

2010

Link zum Volltext

Verfügbarkeit prüfen

Membrane-Permeant derivatives of mannose-1-phosphate

Bioorganic & medicinal chemistry, 2002-12, Vol.10 (12), p.4043-4049

2002

Link zum Volltext

Verfügbarkeit prüfen

Evolution on SoC Integration: GSM Baseband-Radio in 0.13 \mu} CMOS Extended by Fully Integrated Power Management Unit

IEEE journal of solid-state circuits, 2008-01, Vol.43 (1), p.236-245

2008

Link zum Volltext
IEEE_Xplore

Molecular and clinical characterization of a Moroccan Cog7 deficient patient

Molecular genetics and metabolism, 2007-06, Vol.91 (2), p.201-204

2007

Link zum Volltext

Verfügbarkeit prüfen

CDG-Id in two siblings with partially different phenotypes

American journal of medical genetics. Part A, 2007-07, Vol.143A (13), p.1414-1420

2007

Link zum Volltext

Verfügbarkeit prüfen

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

Current Protocols in Immunology, 2008-11, Vol.83 (1), p.8.15.1-8.15.26

2008

Link zum Volltext

Verfügbarkeit prüfen

cyclo Saligenyl‐mannose‐1‐monophosphates as a New Strategy in CDG‐Ia Therapy: Hydrolysis, Mechanistic Insights and Biological Activity

European journal of organic chemistry, 2004-03, Vol.2004 (6), p.1228-1235

2004

Link zum Volltext

Verfügbarkeit prüfen

Endoglycosidase and Glycoamidase Release of N‐Linked Oligosaccharides

Current Protocols in Protein Science, 2006-09, Vol.45 (1), p.12.4.1-12.4.26

2006

Link zum Volltext

Verfügbarkeit prüfen

COG8 deficiency causes new congenital disorder of glycosylation type IIlh

Human molecular genetics, 2007, Vol.16 (7), p.731-741

2007

Link zum Volltext

Verfügbarkeit prüfen

A GSM Baseband Radio in 0.13μm CMOS with Fully Integrated Power-Management

2007 IEEE International Solid-State Circuits Conference. Digest of Technical Papers, 2007, p.264-602

2007

Link zum Volltext
IEEE_Xplore

1 – 25 von 166

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(136)
Mit Volltextzugriff
(155)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(156)
Japanisch
(18)
Deutsch
(10)
Norwegisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(102)
Life Sciences & Biomedicine
(87)
Humans
(76)
Male
(57)
Female
(52)
Adult
(39)
Neurosciences & Neurology
(26)
Biological And Medical Sciences
(23)
Neurosciences
(23)
Young Adult
(23)
Magnetic Resonance Imaging
(21)
Glycosylation
(16)
Medical Sciences
(16)
Animals
(15)
Middle Aged
(15)
Radiology, Nuclear Medicine & Medical Imaging
(13)
Brain Mapping
(12)
Neuroimaging
(12)
Aged
(11)
Adolescent
(10)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Agm1/Pgm3-Mediated Sugar Nucleotide Synthesis Is Essential for Hematopoiesis and Development

A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)

Hypoglycosylation due to dolichol metabolism defects

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

cycloSaligenyl-mannose-1-monophosphates as a New Strategy in CDG-Ia Therapy: Hydrolysis, Mechanistic Insights and Biological Activity

Evolution on SoC Integration : GSM Baseband-Radio in 0.13 μm CMOS Extended by Fully Integrated Power Management Unit

A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy

COG8 deficiency causes new congenital disorder of glycosylation type IIh

A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

Congenital Disorder of Glycosylation Type Ik (CDG-Ik): A Defect of Mannosyltransferase I

Expanding spectrum of congenital disorder of glycosylation Ig (CDG‐Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality

An activated 5′ cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id)

Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS)

Congenital disorder of glycosylation type Id : Clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

Membrane-Permeant derivatives of mannose-1-phosphate

Evolution on SoC Integration: GSM Baseband-Radio in 0.13 \mu} CMOS Extended by Fully Integrated Power Management Unit

Molecular and clinical characterization of a Moroccan Cog7 deficient patient

CDG-Id in two siblings with partially different phenotypes

Endoglycosidase and Glycoamidase Release of N‐Linked Glycans

cyclo Saligenyl‐mannose‐1‐monophosphates as a New Strategy in CDG‐Ia Therapy: Hydrolysis, Mechanistic Insights and Biological Activity

Endoglycosidase and Glycoamidase Release of N‐Linked Oligosaccharides

COG8 deficiency causes new congenital disorder of glycosylation type IIlh

A GSM Baseband Radio in 0.13μm CMOS with Fully Integrated Power-Management

Suchergebnisse filtern