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Biochemical and Biophysical Research Communications|May 30, 2006
Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondriaAnne-Marie Lamhonwah, Ingrid Tein
Clinical Case Reports|March 14, 2018
Novel myophosphorylase mutation (p.Arg94Pro) with progressive exercise intoleranceMaryam Nabavi Nouri, Anne-Marie Lamhonwah, Ingrid Tein
Muscle & Nerve|October 12, 2012
The mdx mouse as a model for carnitine deficiency in the pathogenesis of Duchenne muscular dystrophyZarazuela Zolkipli, Lydia Mai, Anne-Marie Lamhonwah, et al.
Pathology, Research and Practice|February 24, 2009
Organic cation/carnitine transporter family expression patterns in adult murine heartAnne Marie Lamhonwah, Jeannie Wong, Carolyn Tam, et al.
Biochemical and Biophysical Research Communications|January 22, 2003
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5)Anne-Marie Lamhonwah, Jennifer Skaug, Stephen W Scherer, et al.
Biochemical and Biophysical Research Communications|June 6, 2003
Characterization of organic cation/carnitine transporter family in human spermWanli Xuan, Anne-Marie Lamhonwah, Clifford Librach, et al.
Clinical Case Reports|April 12, 2018
Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449)Anne-Marie Lamhonwah, Ivo Barić, Jessica Lamhonwah, et al.
Biochemical and Biophysical Research Communications|December 29, 2010
Upregulation of mammary gland OCTNs maintains carnitine homeostasis in suckling infantsAnne-Marie Lamhonwah, Lydia Mai, Cilla Chung, et al.
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