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Showing results (461-470 of 551) with videos related to

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Human Molecular Genetics|June 22, 2014
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani familyMuzammil A Khan, Verena M Rupp, Meritxell Orpinell, et al.
Psychiatry Research|July 19, 2022
Epigenetic age dysregulation in individuals with bipolar disorder and schizophreniaRichie Jeremian, Alexandra Malinowski, Zanib Chaudhary, et al.
Addictive Behaviors|July 24, 2017
Perceived academic benefit is associated with nonmedical prescription stimulant use among college studentsAmelia M Arria, Irene M Geisner, M Dolores Cimini, et al.
Journal of Genetics|August 13, 2025
Genetic analysis in a consanguineous MCPH family revealed a refinement of the MCPH12 locus and a founder effect of the recurrent <i>CDK6</i> variant [c.589G>A, p.(Ala197Thr)] in the Pakistani populationMuzammil Ahmad Khan, Jasmin Blatterer, Markus Kuster, et al.
Lupus|October 11, 2018
Urinary B-cell-activating factor of the tumour necrosis factor family (BAFF) in systemic lupus erythematosusF B Vincent, R Kandane-Rathnayake, A Y Hoi, et al.
American Journal of Human Genetics|March 11, 2000
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locusJ B Vincent, M L Neves-Pereira, A D Paterson, et al.
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
Bulletin Du Cancer|August 29, 2006
Challenges in the stratification of breast tumors for tailored therapiesJ-P Thiery, X Sastre-Garau, B Vincent-Salomon, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2006
Sequence variants within exon 1 of MECP2 occur in females with mental retardationChris G Harvey, Sailesh D Menon, Beata Stachowiak, et al.
Plos Neglected Tropical Diseases|May 1, 2018
Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcerQuentin B Vincent, Aziz Belkadi, Cindy Fayard, et al.
Pageof 56

Showing results (461-470 of 551) with videos related to

Sort By:
Pageof 56
Human Molecular Genetics|June 22, 2014
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani familyMuzammil A Khan, Verena M Rupp, Meritxell Orpinell, et al.
Psychiatry Research|July 19, 2022
Epigenetic age dysregulation in individuals with bipolar disorder and schizophreniaRichie Jeremian, Alexandra Malinowski, Zanib Chaudhary, et al.
Addictive Behaviors|July 24, 2017
Perceived academic benefit is associated with nonmedical prescription stimulant use among college studentsAmelia M Arria, Irene M Geisner, M Dolores Cimini, et al.
Journal of Genetics|August 13, 2025
Genetic analysis in a consanguineous MCPH family revealed a refinement of the MCPH12 locus and a founder effect of the recurrent <i>CDK6</i> variant [c.589G>A, p.(Ala197Thr)] in the Pakistani populationMuzammil Ahmad Khan, Jasmin Blatterer, Markus Kuster, et al.
Lupus|October 11, 2018
Urinary B-cell-activating factor of the tumour necrosis factor family (BAFF) in systemic lupus erythematosusF B Vincent, R Kandane-Rathnayake, A Y Hoi, et al.
American Journal of Human Genetics|March 11, 2000
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locusJ B Vincent, M L Neves-Pereira, A D Paterson, et al.
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
Bulletin Du Cancer|August 29, 2006
Challenges in the stratification of breast tumors for tailored therapiesJ-P Thiery, X Sastre-Garau, B Vincent-Salomon, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2006
Sequence variants within exon 1 of MECP2 occur in females with mental retardationChris G Harvey, Sailesh D Menon, Beata Stachowiak, et al.
Plos Neglected Tropical Diseases|May 1, 2018
Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcerQuentin B Vincent, Aziz Belkadi, Cindy Fayard, et al.
Pageof 56