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Showing results (31-40 of 329) with videos related to

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Journal of the American Academy of Dermatology|July 28, 2010
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 reportSilke Redler, Roland Kruse, Sibylle Eigelshoven, et al.
Neurobiology of Disease|September 11, 2013
Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampiTanja Grimminger, Katharina Pernhorst, Rainer Surges, et al.
Journal of Neurosurgical Anesthesiology|December 2, 2020
Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical PatientsMarc Rickenbacher, Céline S Reinbold, Stefan Herms, et al.
Archives of Dermatological Research|March 21, 2007
Identification of mutations in the human hairless gene in two new families with congenital atrichiaRegina C Betz, Margarita Indelman, Jana Pforr, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|May 20, 2021
Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2Ulrike Förster-Ruhrmann, Greta Pierchalla, Christiane Stieber, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|July 21, 2021
Untersuchung genetischer Einflüsse auf Riechstörungen bei Patienten mit hereditärem Angioödem Typ 1 und 2Ulrike Förster-Ruhrmann, Greta Pierchalla, Christiane Stieber, et al.
The Journal of Allergy and Clinical Immunology. Global|March 6, 2024
Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiencyDenis Vincent, Faidra Parsopoulou, Ludovic Martin, et al.
Psychiatric Genetics|August 22, 2014
Smoking behaviour: investigation of the coaction of environmental and genetic risk factorsJens Treutlein, Jana Strohmaier, Josef Frank, et al.
Psychiatric Genetics|December 1, 2010
Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sampleChady Abboud Leon, Johannes Schumacher, Nadine Kluck, et al.
Journal of Neuropathology and Experimental Neurology|November 16, 2011
Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampiKatharina Pernhorst, Anna Raabe, Pitt Niehusmann, et al.
Pageof 33

Showing results (31-40 of 329) with videos related to

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Pageof 33
Journal of the American Academy of Dermatology|July 28, 2010
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 reportSilke Redler, Roland Kruse, Sibylle Eigelshoven, et al.
Neurobiology of Disease|September 11, 2013
Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampiTanja Grimminger, Katharina Pernhorst, Rainer Surges, et al.
Journal of Neurosurgical Anesthesiology|December 2, 2020
Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical PatientsMarc Rickenbacher, Céline S Reinbold, Stefan Herms, et al.
Archives of Dermatological Research|March 21, 2007
Identification of mutations in the human hairless gene in two new families with congenital atrichiaRegina C Betz, Margarita Indelman, Jana Pforr, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|May 20, 2021
Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2Ulrike Förster-Ruhrmann, Greta Pierchalla, Christiane Stieber, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|July 21, 2021
Untersuchung genetischer Einflüsse auf Riechstörungen bei Patienten mit hereditärem Angioödem Typ 1 und 2Ulrike Förster-Ruhrmann, Greta Pierchalla, Christiane Stieber, et al.
The Journal of Allergy and Clinical Immunology. Global|March 6, 2024
Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiencyDenis Vincent, Faidra Parsopoulou, Ludovic Martin, et al.
Psychiatric Genetics|August 22, 2014
Smoking behaviour: investigation of the coaction of environmental and genetic risk factorsJens Treutlein, Jana Strohmaier, Josef Frank, et al.
Psychiatric Genetics|December 1, 2010
Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sampleChady Abboud Leon, Johannes Schumacher, Nadine Kluck, et al.
Journal of Neuropathology and Experimental Neurology|November 16, 2011
Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampiKatharina Pernhorst, Anna Raabe, Pitt Niehusmann, et al.
Pageof 33