Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis

Por Rivera, Alicia, Kam, Siok Yuen, Ho, Mengfatt, Romero, Jose R., Lee, Soohee
Publicado em 2012

Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis

Por Bejaoui, Khemissa, Uchida, Yoshikazu, Yasuda, Satoshi, Ho, Mengfatt, Nishijima, Masahiro, Brown, Robert H., Holleran, Walter M., Hanada, Kentaro
Publicado em 2002

Giant Axon Formation in Mice Lacking Kell, XK, or Kell and XK: Animal Models of McLeod Neuroacanthocytosis Syndrome

Por Zhu, Xiang, Cho, Eun-Sook, Sha, Quan, Peng, Jianbin, Oksov, Yelena, Kam, Siok Yuen, Ho, Mengfatt, Walker, Ruth H., Lee, Soohee
Publicado em 2014