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Showing results (141-150 of 282) with videos related to

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American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneH Omran, K Häffner, A Völkel, et al.
Neurology|September 1, 1995
Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsiesT Sander, D Janz, C Ramel, et al.
The Journal of Investigative Dermatology|February 4, 2006
Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritisUlrike Hüffmeier, André Reis, Michael Steffens, et al.
American Journal of Human Genetics|September 14, 2000
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13Y A Lee, F Rüschendorf, C Windemuth, et al.
American Journal of Medical Genetics|June 28, 2001
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paragangliomaS Niemann, J Becker-Follmann, G Nürnberg, et al.
American Journal of Human Genetics|March 1, 1997
Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish familyS Bähring, T Nagai, H R Toka, et al.
Journal of Neurochemistry|November 19, 2013
Analysis of quantitative trait loci in mice suggests a role of Enoph1 in stress reactivityAlexander Barth, Andras Bilkei-Gorzo, Eva Drews, et al.
Infection|March 24, 2024
Hypercalcemia as a rare manifestation of immune reconstitution inflammatory syndrome (IRIS) in a person living with Human Immunodeficiency Virus (HIV) with disseminated nontuberculous mycobacteriosisMaximilian Webendoerfer, Margarethe Konik, Markus Zettler, et al.
American Journal of Human Genetics|March 1, 1997
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21K Saar, K H Chrzanowska, M Stumm, et al.
Archives of Iranian Medicine|October 8, 2015
Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with AtaxiaRoshanak Jazayeri, Hao Hu, Zohreh Fattahi, et al.
Pageof 29

Showing results (141-150 of 282) with videos related to

Sort By:
Pageof 29
American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneH Omran, K Häffner, A Völkel, et al.
Neurology|September 1, 1995
Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsiesT Sander, D Janz, C Ramel, et al.
The Journal of Investigative Dermatology|February 4, 2006
Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritisUlrike Hüffmeier, André Reis, Michael Steffens, et al.
American Journal of Human Genetics|September 14, 2000
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13Y A Lee, F Rüschendorf, C Windemuth, et al.
American Journal of Medical Genetics|June 28, 2001
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paragangliomaS Niemann, J Becker-Follmann, G Nürnberg, et al.
American Journal of Human Genetics|March 1, 1997
Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish familyS Bähring, T Nagai, H R Toka, et al.
Journal of Neurochemistry|November 19, 2013
Analysis of quantitative trait loci in mice suggests a role of Enoph1 in stress reactivityAlexander Barth, Andras Bilkei-Gorzo, Eva Drews, et al.
Infection|March 24, 2024
Hypercalcemia as a rare manifestation of immune reconstitution inflammatory syndrome (IRIS) in a person living with Human Immunodeficiency Virus (HIV) with disseminated nontuberculous mycobacteriosisMaximilian Webendoerfer, Margarethe Konik, Markus Zettler, et al.
American Journal of Human Genetics|March 1, 1997
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21K Saar, K H Chrzanowska, M Stumm, et al.
Archives of Iranian Medicine|October 8, 2015
Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with AtaxiaRoshanak Jazayeri, Hao Hu, Zohreh Fattahi, et al.
Pageof 29