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L Ashmarina

Showing results (1-10 of 6) with videos related to

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Human Molecular Genetics|November 18, 1998
3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient miceS P Wang, J D Marth, L L Oligny, et al.
Biochemical Society Transactions|July 3, 1998
Inborn errors of ketogenesisG A Mitchell, S P Wang, L Ashmarina, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|June 1, 1995
Medical aspects of ketone body metabolismG A Mitchell, S Kassovska-Bratinova, Y Boukaftane, et al.
Cell Death and Differentiation|August 5, 2006
Altered gene expression in cells from patients with lysosomal storage disorders suggests impairment of the ubiquitin pathwayP Bifsha, K Landry, L Ashmarina, et al.
American Journal of Human Genetics|April 16, 1998
HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41QG A Mitchell, P T Ozand, M F Robert, et al.
Pediatric Research|March 3, 2001
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patientsL Bouchard, M F Robert, D Vinarov, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|November 18, 1998
3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient miceS P Wang, J D Marth, L L Oligny, et al.
Biochemical Society Transactions|July 3, 1998
Inborn errors of ketogenesisG A Mitchell, S P Wang, L Ashmarina, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|June 1, 1995
Medical aspects of ketone body metabolismG A Mitchell, S Kassovska-Bratinova, Y Boukaftane, et al.
Cell Death and Differentiation|August 5, 2006
Altered gene expression in cells from patients with lysosomal storage disorders suggests impairment of the ubiquitin pathwayP Bifsha, K Landry, L Ashmarina, et al.
American Journal of Human Genetics|April 16, 1998
HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41QG A Mitchell, P T Ozand, M F Robert, et al.
Pediatric Research|March 3, 2001
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patientsL Bouchard, M F Robert, D Vinarov, et al.
Pageof 1