Laila Begum

The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

Keiko Kobayashi, David S. Sinasac, Mikio Iijima et al. · Nature Genetics · 1999 · 409 citations

Mitochondrial Biogenesis, Mitochondrial Function, Genetic Disorder +9

Reduced N-Acetylaspartate Levels in Mice Lacking Aralar, a Brain- and Muscle-type Mitochondrial Aspartate-glutamate Carrier

Md. Abdul Jalil, Laila Begum, Laura Contreras et al. · Journal of Biological Chemistry · 2005 · 164 citations · Full text

Cellular Physiology, Social Sciences, Oxidative Stress +22

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients

Hong‐Zhi Gao, Keiko Kobayashi, Ayako Tabata et al. · Human Mutation · 2003 · 83 citations

Argininosuccinate Synthetase Gene, Classical Citrullinemia Patients, Genetic Disorder +15

<i>Slc25a13</i>-Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia

David S. Sinasac, Mitsuaki Moriyama, Md. Abdul Jalil et al. · Molecular and Cellular Biology · 2003 · 80 citations · Full text

Metabolic Disorder, Genetics, Immunology +22

Disease‐Modifying Osteoarthritis Treatment With Interleukin‐1 Receptor Antagonist Gene Therapy in Small and Large Animal Models

Alan J. Nixon, Matthew W. Grol, Hayley M. Lang et al. · Arthritis & Rheumatology · 2018 · 72 citations