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Development Genes and Evolution
|
June 8, 2007
The olig family: phylogenetic analysis and early gene expression in Xenopus tropicalis
O J Bronchain, N Pollet, Q Ymlahi-Ouazzani, et al.
Journal of Neuropathology and Experimental Neurology
|
February 5, 2019
Severe Neonatal RYR1 Myopathy With Pathological Features of Congenital Muscular Dystrophy
Daniel C Helbling, David Mendoza, Julie McCarrier, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
January 29, 2015
A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia
G C Geddes, D P Dimmock, D A Hehir, et al.
Psychoneuroendocrinology
|
September 23, 2014
Role of corticosteroid binding globulin in emotional reactivity sex differences in mice
A M Minni, G F de Medeiros, J C Helbling, et al.
Journal of Agricultural and Food Chemistry
|
January 7, 2009
Persistence of plant DNA sequences in the blood of dairy cows fed with genetically modified (Bt176) and conventional corn silage
Y Bertheau, J C Helbling, M N Fortabat, et al.
Journal of Inherited Metabolic Disease
|
December 28, 2020
The nucleotide prodrug CERC-913 improves mtDNA content in primary hepatocytes from DGUOK-deficient rats
Mark A Vanden Avond, Hui Meng, Margaret J Beatka, et al.
Journal of Neuropathology and Experimental Neurology
|
June 1, 2018
Sdha+/- Rats Display Minimal Muscle Pathology Without Significant Behavioral or Biochemical Abnormalities
Emily M Siebers, Melinda J Choi, Jennifer A Tinklenberg, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 8, 2025
Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risks
Stephen F Kingsmore, Gretchen Bandoli, Daniel C Helbling, et al.
American Journal of Medical Genetics. Part A
|
February 2, 2018
Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant
Daniel J Pomerantz, Sacha Ferdinandusse, Joy Cogan, et al.
Journal of Pediatric Genetics
|
May 13, 2017
Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic
David Bick, Pamela C Fraser, Michael F Gutzeit, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Development Genes and Evolution
|
June 8, 2007
The olig family: phylogenetic analysis and early gene expression in Xenopus tropicalis
O J Bronchain, N Pollet, Q Ymlahi-Ouazzani, et al.
Journal of Neuropathology and Experimental Neurology
|
February 5, 2019
Severe Neonatal RYR1 Myopathy With Pathological Features of Congenital Muscular Dystrophy
Daniel C Helbling, David Mendoza, Julie McCarrier, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
January 29, 2015
A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia
G C Geddes, D P Dimmock, D A Hehir, et al.
Psychoneuroendocrinology
|
September 23, 2014
Role of corticosteroid binding globulin in emotional reactivity sex differences in mice
A M Minni, G F de Medeiros, J C Helbling, et al.
Journal of Agricultural and Food Chemistry
|
January 7, 2009
Persistence of plant DNA sequences in the blood of dairy cows fed with genetically modified (Bt176) and conventional corn silage
Y Bertheau, J C Helbling, M N Fortabat, et al.
Journal of Inherited Metabolic Disease
|
December 28, 2020
The nucleotide prodrug CERC-913 improves mtDNA content in primary hepatocytes from DGUOK-deficient rats
Mark A Vanden Avond, Hui Meng, Margaret J Beatka, et al.
Journal of Neuropathology and Experimental Neurology
|
June 1, 2018
Sdha+/- Rats Display Minimal Muscle Pathology Without Significant Behavioral or Biochemical Abnormalities
Emily M Siebers, Melinda J Choi, Jennifer A Tinklenberg, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 8, 2025
Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risks
Stephen F Kingsmore, Gretchen Bandoli, Daniel C Helbling, et al.
American Journal of Medical Genetics. Part A
|
February 2, 2018
Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant
Daniel J Pomerantz, Sacha Ferdinandusse, Joy Cogan, et al.
Journal of Pediatric Genetics
|
May 13, 2017
Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic
David Bick, Pamela C Fraser, Michael F Gutzeit, et al.
Page
of 3