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Michel Guipponi

Showing results (21-30 of 83) with videos related to

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Human Molecular Genetics|December 21, 2012
Tmprss3 loss of function impairs cochlear inner hair cell Kcnma1 channel membrane expressionLaurence Molina, Lydie Fasquelle, Régis Nouvian, et al.
BMC Genetics|September 27, 2013
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous familyNejla Belhedi, Frédérique Bena, Amel Mrabet, et al.
The American Journal of Pathology|July 11, 2007
Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing lossMichel Guipponi, Justin Tan, Ping Z F Cannon, et al.
Plos One|March 17, 2011
Chromosome conformation capture uncovers potential genome-wide interactions between human conserved non-coding sequencesDaniel Robyr, Marc Friedli, Corinne Gehrig, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 17, 2013
Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorderKatherine E Tansey, Michel Guipponi, Enrico Domenici, et al.
Haematologica|July 1, 2021
A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish familyMichel Guipponi, Frédéric Masclaux, Frédérique Sloan-Béna, et al.
Biological Psychiatry|December 15, 2012
Contribution of common genetic variants to antidepressant responseKatherine E Tansey, Michel Guipponi, Xiaolan Hu, et al.
American Journal of Medical Genetics. Part A|February 11, 2020
SCN8A heterozygous variants are associated with anoxic-epileptic seizuresEmmanuelle Ranza, Werner Z'Graggen, Mathias Lidgren, et al.
Bone|September 3, 2014
Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasiaMarie-Hélène Gannagé-Yared, Periklis Makrythanasis, Eliane Chouery, et al.
Plos One|May 9, 2015
HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES CellsAudrey Letourneau, Gilda Cobellis, Alexandre Fort, et al.
Pageof 9

Showing results (21-30 of 83) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|December 21, 2012
Tmprss3 loss of function impairs cochlear inner hair cell Kcnma1 channel membrane expressionLaurence Molina, Lydie Fasquelle, Régis Nouvian, et al.
BMC Genetics|September 27, 2013
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous familyNejla Belhedi, Frédérique Bena, Amel Mrabet, et al.
The American Journal of Pathology|July 11, 2007
Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing lossMichel Guipponi, Justin Tan, Ping Z F Cannon, et al.
Plos One|March 17, 2011
Chromosome conformation capture uncovers potential genome-wide interactions between human conserved non-coding sequencesDaniel Robyr, Marc Friedli, Corinne Gehrig, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 17, 2013
Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorderKatherine E Tansey, Michel Guipponi, Enrico Domenici, et al.
Haematologica|July 1, 2021
A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish familyMichel Guipponi, Frédéric Masclaux, Frédérique Sloan-Béna, et al.
Biological Psychiatry|December 15, 2012
Contribution of common genetic variants to antidepressant responseKatherine E Tansey, Michel Guipponi, Xiaolan Hu, et al.
American Journal of Medical Genetics. Part A|February 11, 2020
SCN8A heterozygous variants are associated with anoxic-epileptic seizuresEmmanuelle Ranza, Werner Z'Graggen, Mathias Lidgren, et al.
Bone|September 3, 2014
Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasiaMarie-Hélène Gannagé-Yared, Periklis Makrythanasis, Eliane Chouery, et al.
Plos One|May 9, 2015
HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES CellsAudrey Letourneau, Gilda Cobellis, Alexandre Fort, et al.
Pageof 9