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Wienker

Showing results (191-200 of 282) with videos related to

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Hypertension (Dallas, Tex. : 1979)|December 1, 1996
Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertensionH Schuster, T F Wienker, H R Toka, et al.
Tissue Antigens|March 11, 2011
Caspase recruitment domain 15 gene haplotypes in sarcoidosisS Pabst, M Golebiewski, S Herms, et al.
Journal of the American Academy of Dermatology|March 21, 2006
Familial aggregation of alopecia areataBettina Blaumeiser, Ineke van der Goot, Rolf Fimmers, et al.
Scientific Reports|April 24, 2024
Elexacaftor/tezacaftor/ivacaftor influences body composition in adults with cystic fibrosis: a fully automated CT-based analysisDirk Westhölter, Johannes Haubold, Matthias Welsner, et al.
Nature Genetics|December 2, 2000
A major susceptibility locus for atopic dermatitis maps to chromosome 3q21Y A Lee, U Wahn, R Kehrt, et al.
Epilepsy Research|April 1, 1996
Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5T Sander, T Hildmann, D Janz, et al.
Human Mutation|February 26, 2017
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disabilityLuciana Musante, Lucia Püttmann, Kimia Kahrizi, et al.
Elife|August 7, 2016
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentationBianca Hartmann, Timothy Wai, Hao Hu, et al.
Human Heredity|April 2, 2010
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction testsMichael Steffens, Tim Becker, Thomas Sander, et al.
The International Journal of Neuropsychopharmacology|August 16, 2005
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorderJobst Meyer, Kirsten Johannssen, Christine M Freitag, et al.
Pageof 29

Showing results (191-200 of 282) with videos related to

Sort By:
Pageof 29
Hypertension (Dallas, Tex. : 1979)|December 1, 1996
Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertensionH Schuster, T F Wienker, H R Toka, et al.
Tissue Antigens|March 11, 2011
Caspase recruitment domain 15 gene haplotypes in sarcoidosisS Pabst, M Golebiewski, S Herms, et al.
Journal of the American Academy of Dermatology|March 21, 2006
Familial aggregation of alopecia areataBettina Blaumeiser, Ineke van der Goot, Rolf Fimmers, et al.
Scientific Reports|April 24, 2024
Elexacaftor/tezacaftor/ivacaftor influences body composition in adults with cystic fibrosis: a fully automated CT-based analysisDirk Westhölter, Johannes Haubold, Matthias Welsner, et al.
Nature Genetics|December 2, 2000
A major susceptibility locus for atopic dermatitis maps to chromosome 3q21Y A Lee, U Wahn, R Kehrt, et al.
Epilepsy Research|April 1, 1996
Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5T Sander, T Hildmann, D Janz, et al.
Human Mutation|February 26, 2017
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disabilityLuciana Musante, Lucia Püttmann, Kimia Kahrizi, et al.
Elife|August 7, 2016
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentationBianca Hartmann, Timothy Wai, Hao Hu, et al.
Human Heredity|April 2, 2010
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction testsMichael Steffens, Tim Becker, Thomas Sander, et al.
The International Journal of Neuropsychopharmacology|August 16, 2005
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorderJobst Meyer, Kirsten Johannssen, Christine M Freitag, et al.
Pageof 29