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Sabine Strahl

Name	Sabine Strahl
Ort	Heidelberg (Wirkungsort) Deutschland
Geschlecht	weiblich
Akademischer Grad bzw. Titel	Prof. Dr.
Variante	Sabine Stahl (falsche Namensform) Sabine Strahl-Bolsinger Sabine Strahl- Bolsinger
Beziehung	Universität Heidelberg. Centre for Organismal Studies
Weitere Angaben	Arbeitsgebiet: Zellchemie
Datensatztyp	Person
GND-Nummer	1034793055
Datensatz-ID	1034793055
Beteiligt an alle anzeigen Biallelische Varianten in GZF1 und VPS45 verbinden das Larsen-Syndrom mit den `Congenital Disorders of Glycosylation´ (CDG) Study of protein O-mannosylation in the context of endoplasmic reticulum protein homeostasis Corrigendum: Induction of Antibodies Directed Against Branched Core O ‐Mannosyl Glycopeptides—Selectivity Complimentary to the ConA Lectin Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG Induction of Antibodies Directed Against Branched Core O ‐Mannosyl Glycopeptides—Selectivity Complimentary to the ConA Lectin Klinische, molekularbiologische und biochemische Charakterisierung eines neuen Patientendefekts im „ATPase H+-transporting accessory protein 1“ (ATP6AP1)-Gen Identifizierung und Charakterisierung fukosylierter Proteine sowie Untersuchungen zur Fukosetherapie in einem Mausmodell zu der humanen Erberkrankung SLC35C1-CDG The genetic interaction network of CCW12, a Saccharomyces cerevisiae gene required for cell wall integrity during budding and formation of mating projections Protein Glycosylation, Conserved from Yeast to Man: A Model Organism Helps Elucidate Congenital Human Diseases Protein Glycosylation, Conserved from Yeast to Man: A Model Organism Helps Elucidate Congenital Human Diseases O ‐Mannosylation precedes and potentially controls the N ‐glycosylation of a yeast cell wall glycoprotein

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Katalog der Deutschen Nationalbibliothek

Sabine Strahl

Biallelische Varianten in GZF1 und VPS45 verbinden das Larsen-Syndrom mit den `Congenital Disorders of Glycosylation´ (CDG)

Study of protein O-mannosylation in the context of endoplasmic reticulum protein homeostasis

Corrigendum: Induction of Antibodies Directed Against Branched Core O ‐Mannosyl Glycopeptides—Selectivity Complimentary to the ConA Lectin

Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG

Induction of Antibodies Directed Against Branched Core O ‐Mannosyl Glycopeptides—Selectivity Complimentary to the ConA Lectin

Klinische, molekularbiologische und biochemische Charakterisierung eines neuen Patientendefekts im „ATPase H+-transporting accessory protein 1“ (ATP6AP1)-Gen

Identifizierung und Charakterisierung fukosylierter Proteine sowie Untersuchungen zur Fukosetherapie in einem Mausmodell zu der humanen Erberkrankung SLC35C1-CDG

The genetic interaction network of CCW12, a Saccharomyces cerevisiae gene required for cell wall integrity during budding and formation of mating projections

Protein Glycosylation, Conserved from Yeast to Man: A Model Organism Helps Elucidate Congenital Human Diseases

Protein Glycosylation, Conserved from Yeast to Man: A Model Organism Helps Elucidate Congenital Human Diseases

O ‐Mannosylation precedes and potentially controls the N ‐glycosylation of a yeast cell wall glycoprotein