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Alan Hodgkinson

Showing results (21-30 of 29) with videos related to

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Journal of Psychiatric Research|March 9, 2016
Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophreniaNancy D Merner, Adriana Mercado, Arjun R Khanna, et al.
Nature Communications|March 8, 2018
Gene-by-environment interactions in urban populations modulate risk phenotypesMarie-Julie Favé, Fabien C Lamaze, David Soave, et al.
The Science of the Total Environment|January 16, 2025
Quantification of heavy metal exposure in a British population cohort links total mercury levels in plasma with skin tissue-specific changes in mitochondrial-related gene expressionMarcel van de Streek, Aminah Tasnim Ali, Julia S El-Sayed Moustafa, et al.
Genetics|December 1, 2017
Relaxed Selection During a Recent Human ExpansionStephan Peischl, Isabelle Dupanloup, Adrien Foucal, et al.
Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.
Genome Biology|February 15, 2022
Genetic variation at mouse and human ribosomal DNA influences associated epigenetic statesFrancisco Rodriguez-Algarra, Robert A E Seaborne, Amy F Danson, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Plos Genetics|October 3, 2013
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humansFerran Casals, Alan Hodgkinson, Julie Hussin, et al.
EMBO Reports|June 15, 2014
Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsyKristopher T Kahle, Nancy D Merner, Perrine Friedel, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of Psychiatric Research|March 9, 2016
Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophreniaNancy D Merner, Adriana Mercado, Arjun R Khanna, et al.
Nature Communications|March 8, 2018
Gene-by-environment interactions in urban populations modulate risk phenotypesMarie-Julie Favé, Fabien C Lamaze, David Soave, et al.
The Science of the Total Environment|January 16, 2025
Quantification of heavy metal exposure in a British population cohort links total mercury levels in plasma with skin tissue-specific changes in mitochondrial-related gene expressionMarcel van de Streek, Aminah Tasnim Ali, Julia S El-Sayed Moustafa, et al.
Genetics|December 1, 2017
Relaxed Selection During a Recent Human ExpansionStephan Peischl, Isabelle Dupanloup, Adrien Foucal, et al.
Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.
Genome Biology|February 15, 2022
Genetic variation at mouse and human ribosomal DNA influences associated epigenetic statesFrancisco Rodriguez-Algarra, Robert A E Seaborne, Amy F Danson, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Plos Genetics|October 3, 2013
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humansFerran Casals, Alan Hodgkinson, Julie Hussin, et al.
EMBO Reports|June 15, 2014
Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsyKristopher T Kahle, Nancy D Merner, Perrine Friedel, et al.
Pageof 3