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Donna M Martin

Showing results (31-40 of 104) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 1, 2014
CHD7 mutations and CHARGE syndrome in semicircular canal dysplasiaGlenn E Green, Farhan S Huq, Sarah B Emery, et al.
Developmental Biology|November 28, 2002
Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepitheliumDonna M Martin, Jennifer M Skidmore, Sharon E Fox, et al.
Pediatric Neurology|January 8, 2013
Leigh syndrome in a girl with a novel DLD mutation causing E3 deficiencyShane C Quinonez, Steven M Leber, Donna M Martin, et al.
Pediatric Neurology|January 25, 2005
Brain glutamine by MRS in a patient with urea cycle disorder and comaJasna Kojic, Patricia L Robertson, Douglas J Quint, et al.
Genesis (New York, N.Y. : 2000)|July 11, 2006
Nestin-Cre mediated deletion of Pitx2 in the mouseAnthony M Sclafani, Jennifer M Skidmore, Hemanth Ramaprakash, et al.
Developmental Cognitive Neuroscience|January 16, 2017
The influence of 5-HTTLPR transporter genotype on amygdala-subgenual anterior cingulate cortex connectivity in autism spectrum disorderFrancisco Velasquez, Jillian Lee Wiggins, Whitney I Mattson, et al.
Stem Cell Research|January 15, 2026
Generation of induced pluripotent stem cells from a patient with CHARGE syndrome with athymia, harboring a heterozygous mutation in CHD7Jin Zhao, Rong Hu, Kuan Chen Lai, et al.
American Journal of Medical Genetics. Part A|April 11, 2014
Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletionAndrea H Seeley, Mark A Durham, Mark A Micale, et al.
Human Brain Mapping|November 6, 2012
Age-related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescenceJillian Lee Wiggins, Jirair K Bedoyan, Melisa Carrasco, et al.
Frontiers in Genetics|November 22, 2018
Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the <i>Chd7</i> Mutant Mouse EarRobert Durruthy-Durruthy, Ethan D Sperry, Margot E Bowen, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 1, 2014
CHD7 mutations and CHARGE syndrome in semicircular canal dysplasiaGlenn E Green, Farhan S Huq, Sarah B Emery, et al.
Developmental Biology|November 28, 2002
Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepitheliumDonna M Martin, Jennifer M Skidmore, Sharon E Fox, et al.
Pediatric Neurology|January 8, 2013
Leigh syndrome in a girl with a novel DLD mutation causing E3 deficiencyShane C Quinonez, Steven M Leber, Donna M Martin, et al.
Pediatric Neurology|January 25, 2005
Brain glutamine by MRS in a patient with urea cycle disorder and comaJasna Kojic, Patricia L Robertson, Douglas J Quint, et al.
Genesis (New York, N.Y. : 2000)|July 11, 2006
Nestin-Cre mediated deletion of Pitx2 in the mouseAnthony M Sclafani, Jennifer M Skidmore, Hemanth Ramaprakash, et al.
Developmental Cognitive Neuroscience|January 16, 2017
The influence of 5-HTTLPR transporter genotype on amygdala-subgenual anterior cingulate cortex connectivity in autism spectrum disorderFrancisco Velasquez, Jillian Lee Wiggins, Whitney I Mattson, et al.
Stem Cell Research|January 15, 2026
Generation of induced pluripotent stem cells from a patient with CHARGE syndrome with athymia, harboring a heterozygous mutation in CHD7Jin Zhao, Rong Hu, Kuan Chen Lai, et al.
American Journal of Medical Genetics. Part A|April 11, 2014
Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletionAndrea H Seeley, Mark A Durham, Mark A Micale, et al.
Human Brain Mapping|November 6, 2012
Age-related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescenceJillian Lee Wiggins, Jirair K Bedoyan, Melisa Carrasco, et al.
Frontiers in Genetics|November 22, 2018
Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the <i>Chd7</i> Mutant Mouse EarRobert Durruthy-Durruthy, Ethan D Sperry, Margot E Bowen, et al.
Pageof 11