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Human genetics

Showing results (271-280 of 11,262) with videos related to

Pageof 1,127
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Human Genetics|October 1, 1986
Regional localisation of X chromosome short arm probesK Paulsen, S Forrest, G Scherer, et al.
Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S Malcolm
Human Genetics|October 1, 1986
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1C Turleau, F Taillard, M Doussau de Bazignan, et al.
Human Genetics|December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.
Human Genetics|January 28, 2022
Heat increases full-length SMN splicing: promise for splice-augmenting therapies for SMACatherine E Dominguez, David Cunningham, Akila S Venkataramany, et al.
Human Genetics|January 31, 2022
Evaluating the relevance of sequence conservation in the prediction of pathogenic missense variantsEmidio Capriotti, Piero Fariselli
Human Genetics|November 1, 1986
Chromosome changes in human monocytic cell lines with in vitro spontaneous malignant transformationL Romitti, R P Revoltella, E Vigneti, et al.
Human Genetics|November 1, 1986
Effect of the esterase-D phenotype on its in vitro enzyme activityJ K Cowell, P Rutland, M Jay, et al.
Human Genetics|October 2, 2021
Clinical implementation of drug metabolizing gene-based therapeutic interventions worldwideEvangelia Eirini Tsermpini, Zeina N Al-Mahayri, Bassam R Ali, et al.
Human Genetics|February 19, 2022
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylationEline Blommaert, Natalia A Cherepanova, Frederik Staels, et al.
Pageof 1,127

Showing results (271-280 of 11,262) with videos related to

Sort By:
Pageof 1,127
Human Genetics|October 1, 1986
Regional localisation of X chromosome short arm probesK Paulsen, S Forrest, G Scherer, et al.
Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S Malcolm
Human Genetics|October 1, 1986
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1C Turleau, F Taillard, M Doussau de Bazignan, et al.
Human Genetics|December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.
Human Genetics|January 28, 2022
Heat increases full-length SMN splicing: promise for splice-augmenting therapies for SMACatherine E Dominguez, David Cunningham, Akila S Venkataramany, et al.
Human Genetics|January 31, 2022
Evaluating the relevance of sequence conservation in the prediction of pathogenic missense variantsEmidio Capriotti, Piero Fariselli
Human Genetics|November 1, 1986
Chromosome changes in human monocytic cell lines with in vitro spontaneous malignant transformationL Romitti, R P Revoltella, E Vigneti, et al.
Human Genetics|November 1, 1986
Effect of the esterase-D phenotype on its in vitro enzyme activityJ K Cowell, P Rutland, M Jay, et al.
Human Genetics|October 2, 2021
Clinical implementation of drug metabolizing gene-based therapeutic interventions worldwideEvangelia Eirini Tsermpini, Zeina N Al-Mahayri, Bassam R Ali, et al.
Human Genetics|February 19, 2022
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylationEline Blommaert, Natalia A Cherepanova, Frederik Staels, et al.
Pageof 1,127