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John Dean

Showing results (121-130 of 143) with videos related to

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Orphanet Journal of Rare Diseases|July 21, 2019
Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual DisabilityJill Clayton-Smith, Rebecca Bromley, John Dean, et al.
Nature Neuroscience|January 22, 2019
Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projectionWenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
Nature Neuroscience|June 22, 2019
Author Correction: Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projectionWenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
The Journal of Sexual Medicine|November 6, 2010
International Society for Sexual Medicine's guidelines for the diagnosis and treatment of premature ejaculationStanley E Althof, Carmita H N Abdo, John Dean, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|October 30, 2014
Canadian hereditary angioedema guidelineStephen Betschel, Jacquie Badiou, Karen Binkley, et al.
Nature Genetics|March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndromeLouise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics|October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apneaJanina Sörmann, Marcus Schewe, Peter Proks, et al.
American Journal of Human Genetics|February 1, 2020
Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial MetabolismAdam C Gunning, Klaudia Strucinska, Mikel Muñoz Oreja, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2024
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorderFrançois Lecoquierre, A Mattijs Punt, Frédéric Ebstein, et al.
The Journal of Allergy and Clinical Immunology|September 10, 2004
Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary AngioedemaTom Bowen, Marco Cicardi, Henriette Farkas, et al.
Pageof 15

Showing results (121-130 of 143) with videos related to

Sort By:
Pageof 15
Orphanet Journal of Rare Diseases|July 21, 2019
Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual DisabilityJill Clayton-Smith, Rebecca Bromley, John Dean, et al.
Nature Neuroscience|January 22, 2019
Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projectionWenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
Nature Neuroscience|June 22, 2019
Author Correction: Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projectionWenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
The Journal of Sexual Medicine|November 6, 2010
International Society for Sexual Medicine's guidelines for the diagnosis and treatment of premature ejaculationStanley E Althof, Carmita H N Abdo, John Dean, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|October 30, 2014
Canadian hereditary angioedema guidelineStephen Betschel, Jacquie Badiou, Karen Binkley, et al.
Nature Genetics|March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndromeLouise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics|October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apneaJanina Sörmann, Marcus Schewe, Peter Proks, et al.
American Journal of Human Genetics|February 1, 2020
Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial MetabolismAdam C Gunning, Klaudia Strucinska, Mikel Muñoz Oreja, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2024
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorderFrançois Lecoquierre, A Mattijs Punt, Frédéric Ebstein, et al.
The Journal of Allergy and Clinical Immunology|September 10, 2004
Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary AngioedemaTom Bowen, Marco Cicardi, Henriette Farkas, et al.
Pageof 15