Xue Yang

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency

Xue Yang, Yoko Aoki, Xue Li et al. · Human Genetics · 2001 · 64 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Fatal Propionic Acidemia in Mice Lacking Propionyl-CoA Carboxylase and Its Rescue by Postnatal, Liver-specific Supplementation via a Transgene

Toru Miyazaki, Toshihiro Ohura, Makio Kobayashi et al. · Journal of Biological Chemistry · 2001 · 61 citations · Full text

Linkage and association of childhood asthma with the chromosome 12 genes

Chenchen Shao, Yoichi Suzuki, Fumiaki Kamada et al. · Journal of Human Genetics · 2004 · 46 citations · Full text

Asthma, Allergy, Childhood Asthma +8

Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia

Xue Yang, Osamu Sakamoto, Yoichi Matsubara et al. · Molecular Genetics and Metabolism · 2004 · 35 citations

Propionic Acidemia, Genetics, Inherited Metabolic Disease +7

Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B12-responsive methylmalonic acidemia: identification of a prevalent MMAA mutation

Xue Yang, Osamu Sakamoto, Yoichi Matsubara et al. · Molecular Genetics and Metabolism · 2004 · 33 citations

Genetic Disorder, Medicine, Genetics +8