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Georgia Lahr

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Endocrine Pathology|July 1, 1995
Expression of the Neural Cell Adhesion Molecule NCAM by Peptide- and Steroid-Producing Endocrine Cells and Tumors: Alternatively Spliced Forms and PolysialylationGeorgia Lahr, Artur Mayerhofer
Methods in Enzymology|November 7, 2002
Analysis of specific gene expressionGeorgia Lahr, Anna Starzinski-Powitz, Anette Mayer
Methods in Enzymology|November 7, 2002
Going in vivo with laser microdissectionAnette Mayer, Monika Stich, Dieter Brocksch, et al.
Journal of Medical Case Reports|January 11, 2013
A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: a case seriesBan Mousa Rashid, Nawshirwan Gafoor Rashid, Ansgar Schulz, et al.
Haematologica|September 5, 2007
Codon 104(-G), a dominant beta0-thalassemia-like phenotype in a German Caucasian family is associated with mild chronic hemolytic anemia but influenced in severity by co-inherited genetic factorsGeorgia Lahr, Joaquin Brintrup, Stefan Over, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemiaOzlem Engiz, Semra Kara, Denizhan Bagrul, et al.
Pediatric Research|October 25, 2008
Residual CD95-pathway function in children with autoimmune lymphoproliferative syndrome is independent from clinical state and genotype of CD95 mutationHans Fuchs, Carsten Posovszky, Georgia Lahr, et al.
Molecular and Cellular Pediatrics|November 15, 2015
Monogenic forms of childhood obesity due to mutations in the leptin geneJan-Bernd Funcke, Julia von Schnurbein, Belinda Lennerz, et al.
The Journal of Pediatrics|November 18, 2005
Identical phenotype in patients with somatic and germline CD95 mutations requires a new diagnostic approach to autoimmune lymphoproliferative syndromeJochen Rössler, Anselm Enders, Georgia Lahr, et al.
BMC Gastroenterology|May 3, 2013
Age-of-onset-dependent influence of NOD2 gene variants on disease behaviour and treatment in Crohn's diseaseCarsten Posovszky, Veronika Pfalzer, Georgia Lahr, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Endocrine Pathology|July 1, 1995
Expression of the Neural Cell Adhesion Molecule NCAM by Peptide- and Steroid-Producing Endocrine Cells and Tumors: Alternatively Spliced Forms and PolysialylationGeorgia Lahr, Artur Mayerhofer
Methods in Enzymology|November 7, 2002
Analysis of specific gene expressionGeorgia Lahr, Anna Starzinski-Powitz, Anette Mayer
Methods in Enzymology|November 7, 2002
Going in vivo with laser microdissectionAnette Mayer, Monika Stich, Dieter Brocksch, et al.
Journal of Medical Case Reports|January 11, 2013
A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: a case seriesBan Mousa Rashid, Nawshirwan Gafoor Rashid, Ansgar Schulz, et al.
Haematologica|September 5, 2007
Codon 104(-G), a dominant beta0-thalassemia-like phenotype in a German Caucasian family is associated with mild chronic hemolytic anemia but influenced in severity by co-inherited genetic factorsGeorgia Lahr, Joaquin Brintrup, Stefan Over, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemiaOzlem Engiz, Semra Kara, Denizhan Bagrul, et al.
Pediatric Research|October 25, 2008
Residual CD95-pathway function in children with autoimmune lymphoproliferative syndrome is independent from clinical state and genotype of CD95 mutationHans Fuchs, Carsten Posovszky, Georgia Lahr, et al.
Molecular and Cellular Pediatrics|November 15, 2015
Monogenic forms of childhood obesity due to mutations in the leptin geneJan-Bernd Funcke, Julia von Schnurbein, Belinda Lennerz, et al.
The Journal of Pediatrics|November 18, 2005
Identical phenotype in patients with somatic and germline CD95 mutations requires a new diagnostic approach to autoimmune lymphoproliferative syndromeJochen Rössler, Anselm Enders, Georgia Lahr, et al.
BMC Gastroenterology|May 3, 2013
Age-of-onset-dependent influence of NOD2 gene variants on disease behaviour and treatment in Crohn's diseaseCarsten Posovszky, Veronika Pfalzer, Georgia Lahr, et al.
Pageof 2