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H Sherr

Showing results (191-200 of 290) with videos related to

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JCI Insight|November 9, 2023
TMTC4 is a hair cell-specific human deafness geneJiang Li, Byung Yoon Choi, Yasmin Eltawil, et al.
AIDS (London, England)|December 22, 2009
Quality of HIV care provided by non-physician clinicians and physicians in Mozambique: a retrospective cohort studyKenneth H Sherr, Mark A Micek, Sarah O Gimbel, et al.
Human Mutation|November 19, 2011
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humansAnne M Slavotinek, Ryan Chao, Tomas Vacik, et al.
Cell Reports|October 13, 2016
Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus CallosumIlan Gobius, Laura Morcom, Rodrigo Suárez, et al.
Neurology|March 26, 2003
Periventricular heterotopia associated with chromosome 5p anomaliesV L Sheen, J W Wheless, A Bodell, et al.
Neuroimage. Clinical|September 29, 2015
Abnormal auditory and language pathways in children with 16p11.2 deletionJeffrey I Berman, Darina Chudnovskaya, Lisa Blaskey, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 31, 2012
Children with autism show reduced somatosensory response: an MEG studyElysa J Marco, Kasra Khatibi, Susanna S Hill, et al.
Breast Cancer Research and Treatment|November 30, 2000
Expression of the aryl hydrocarbon receptor/transcription factor (AhR) and AhR-regulated CYP1 gene transcripts in a rat model of mammary tumorigenesisA F Trombino, R I Near, R A Matulka, et al.
Journal of Medical Genetics|January 12, 2020
De novo variants in <i>SUPT16H</i> cause neurodevelopmental disorders associated with corpus callosum abnormalitiesRoya Bina, Dena Matalon, Brieana Fregeau, et al.
Brain Connectivity|September 26, 2013
Resting-state networks and the functional connectome of the human brain in agenesis of the corpus callosumJulia P Owen, Yi-Ou Li, Fanpei G Yang, et al.
Pageof 29

Showing results (191-200 of 290) with videos related to

Sort By:
Pageof 29
JCI Insight|November 9, 2023
TMTC4 is a hair cell-specific human deafness geneJiang Li, Byung Yoon Choi, Yasmin Eltawil, et al.
AIDS (London, England)|December 22, 2009
Quality of HIV care provided by non-physician clinicians and physicians in Mozambique: a retrospective cohort studyKenneth H Sherr, Mark A Micek, Sarah O Gimbel, et al.
Human Mutation|November 19, 2011
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humansAnne M Slavotinek, Ryan Chao, Tomas Vacik, et al.
Cell Reports|October 13, 2016
Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus CallosumIlan Gobius, Laura Morcom, Rodrigo Suárez, et al.
Neurology|March 26, 2003
Periventricular heterotopia associated with chromosome 5p anomaliesV L Sheen, J W Wheless, A Bodell, et al.
Neuroimage. Clinical|September 29, 2015
Abnormal auditory and language pathways in children with 16p11.2 deletionJeffrey I Berman, Darina Chudnovskaya, Lisa Blaskey, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 31, 2012
Children with autism show reduced somatosensory response: an MEG studyElysa J Marco, Kasra Khatibi, Susanna S Hill, et al.
Breast Cancer Research and Treatment|November 30, 2000
Expression of the aryl hydrocarbon receptor/transcription factor (AhR) and AhR-regulated CYP1 gene transcripts in a rat model of mammary tumorigenesisA F Trombino, R I Near, R A Matulka, et al.
Journal of Medical Genetics|January 12, 2020
De novo variants in <i>SUPT16H</i> cause neurodevelopmental disorders associated with corpus callosum abnormalitiesRoya Bina, Dena Matalon, Brieana Fregeau, et al.
Brain Connectivity|September 26, 2013
Resting-state networks and the functional connectome of the human brain in agenesis of the corpus callosumJulia P Owen, Yi-Ou Li, Fanpei G Yang, et al.
Pageof 29