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Raoul Heller

Showing results (1-10 of 45) with videos related to

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Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Uniparental disomies 7 and 14Katrin Hoffmann, Raoul Heller
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 3, 2015
The challenge of defining pathogenicity: the example of AHI1Raoul Heller, Hanno J Bolz
Blood|April 23, 2011
Heterozygous disruption of human SOX6 is insufficient to impair erythropoiesis or silencing of fetal hemoglobinVijay G Sankaran, Jan Menne, Raoul Heller
Molecular Reproduction and Development|November 7, 2002
HE6, a two-subunit heptahelical receptor associated with apical membranes of efferent and epididymal duct epitheliaHeike Obermann, Annemarie Samalecos, Caroline Osterhoff, et al.
Frontiers in Genetics|October 12, 2017
Recurrent and Prolonged Infections in a Child with a Homozygous <i>IFIH1</i> Nonsense MutationMaha Zaki, Michaela Thoenes, Amit Kawalia, et al.
Neuropediatrics|May 24, 2016
Novel Mutations in the Nonselective Sodium Leak Channel (NALCN) Lead to Distal Arthrogryposis with Increased Muscle ToneMert Karakaya, Raoul Heller, Volkmar Kunde, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Maximum bite force in patients with spinal muscular atrophy during the first year of nusinersen therapy - A pilot studyTeresa Kruse, Raoul Heller, Brunhilde Wirth, et al.
Anticancer Research|April 12, 2003
Biological and molecular characterization of a new human ampullary cancer cell lineMatthias Peiper, Ingo Alldinger, Raoul Heller, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findingsAnja Hagen, Arndt Bigl, Dorothea Wand, et al.
Brain : a Journal of Neurology|October 4, 2017
PRUNE1: a disease-causing gene for secondary microcephalyMert Karakaya, Sanem Yilmaz, Markus Storbeck, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Uniparental disomies 7 and 14Katrin Hoffmann, Raoul Heller
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 3, 2015
The challenge of defining pathogenicity: the example of AHI1Raoul Heller, Hanno J Bolz
Blood|April 23, 2011
Heterozygous disruption of human SOX6 is insufficient to impair erythropoiesis or silencing of fetal hemoglobinVijay G Sankaran, Jan Menne, Raoul Heller
Molecular Reproduction and Development|November 7, 2002
HE6, a two-subunit heptahelical receptor associated with apical membranes of efferent and epididymal duct epitheliaHeike Obermann, Annemarie Samalecos, Caroline Osterhoff, et al.
Frontiers in Genetics|October 12, 2017
Recurrent and Prolonged Infections in a Child with a Homozygous <i>IFIH1</i> Nonsense MutationMaha Zaki, Michaela Thoenes, Amit Kawalia, et al.
Neuropediatrics|May 24, 2016
Novel Mutations in the Nonselective Sodium Leak Channel (NALCN) Lead to Distal Arthrogryposis with Increased Muscle ToneMert Karakaya, Raoul Heller, Volkmar Kunde, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Maximum bite force in patients with spinal muscular atrophy during the first year of nusinersen therapy - A pilot studyTeresa Kruse, Raoul Heller, Brunhilde Wirth, et al.
Anticancer Research|April 12, 2003
Biological and molecular characterization of a new human ampullary cancer cell lineMatthias Peiper, Ingo Alldinger, Raoul Heller, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findingsAnja Hagen, Arndt Bigl, Dorothea Wand, et al.
Brain : a Journal of Neurology|October 4, 2017
PRUNE1: a disease-causing gene for secondary microcephalyMert Karakaya, Sanem Yilmaz, Markus Storbeck, et al.
Pageof 5