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Clemer Abad

Showing results (1-10 of 27) with videos related to

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Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|March 23, 2024
Fatal septicemia in 2 South American camelids with caudal C3-pyloric-duodenal adenocarcinomaClemer Abad, Heather Fritz, Omar Gonzales-Viera
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Biology|April 28, 2017
Rai1 Haploinsufficiency Is Associated with Social Abnormalities in MiceNalini R Rao, Clemer Abad, Irene C Perez, et al.
Human Molecular Genetics|November 13, 2013
Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memoryLei Cao, Jessica Molina, Clemer Abad, et al.
Frontiers in Cell and Developmental Biology|October 5, 2020
Bromodomain Protein BRD4 Is Essential for Hair Cell Function and SurvivalAbhiraami Kannan-Sundhari, Clemer Abad, Marie E Maloof, et al.
Human Molecular Genetics|April 1, 2021
Generation and characterization of a P2rx2 V60L mouse model for DFNA41Xiaoya Chen, Clemer Abad, Zheng-Yi Chen, et al.
EMBO Molecular Medicine|July 9, 2014
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndromeVladimir Camarena, Lei Cao, Clemer Abad, et al.
Human Genetics|March 26, 2026
The involvement of TNFRSF25 in age-related hearing lossMarie Valerie Roche, Pei-Ciao Tang, Denise Yan, et al.
Translational Psychiatry|January 18, 2024
Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterningClemer Abad, Maria C Robayo, Maria Del Mar Muñiz-Moreno, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|March 23, 2024
Fatal septicemia in 2 South American camelids with caudal C3-pyloric-duodenal adenocarcinomaClemer Abad, Heather Fritz, Omar Gonzales-Viera
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Biology|April 28, 2017
Rai1 Haploinsufficiency Is Associated with Social Abnormalities in MiceNalini R Rao, Clemer Abad, Irene C Perez, et al.
Human Molecular Genetics|November 13, 2013
Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memoryLei Cao, Jessica Molina, Clemer Abad, et al.
Frontiers in Cell and Developmental Biology|October 5, 2020
Bromodomain Protein BRD4 Is Essential for Hair Cell Function and SurvivalAbhiraami Kannan-Sundhari, Clemer Abad, Marie E Maloof, et al.
Human Molecular Genetics|April 1, 2021
Generation and characterization of a P2rx2 V60L mouse model for DFNA41Xiaoya Chen, Clemer Abad, Zheng-Yi Chen, et al.
EMBO Molecular Medicine|July 9, 2014
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndromeVladimir Camarena, Lei Cao, Clemer Abad, et al.
Human Genetics|March 26, 2026
The involvement of TNFRSF25 in age-related hearing lossMarie Valerie Roche, Pei-Ciao Tang, Denise Yan, et al.
Translational Psychiatry|January 18, 2024
Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterningClemer Abad, Maria C Robayo, Maria Del Mar Muñiz-Moreno, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
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