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Journal of Sleep Research|January 26, 2000
Scalp topography of the auditory evoked K-complex in stage 2 and slow wave sleepK A Cote, D R de Lugt, S D Langley, et al.
The Journal of Biological Chemistry|June 25, 1983
A genetic variant of beta-glucuronidase in Drosophila melanogasterS D Langley, S D Wilson, A S Gross, et al.
Human Mutation|February 5, 1998
Duarte allele impairs biostability of galactose-1-phosphate uridyltransferase in human lymphoblastsK Lai, S D Langley, P P Dembure, et al.
The Journal of Biological Chemistry|June 25, 1992
Activation of insulin receptor signaling by a single amino acid substitution in the transmembrane domainN Longo, R C Shuster, L D Griffin, et al.
American Journal of Human Genetics|February 1, 1997
Molecular basis for Duarte and Los Angeles variant galactosemiaS D Langley, K Lai, P P Dembure, et al.
Glycobiology|March 11, 2003
GALT deficiency causes UDP-hexose deficit in human galactosemic cellsK Lai, S D Langley, F W Khwaja, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1994
Impaired growth in Rabson-Mendenhall syndrome: lack of effect of growth hormone and insulin-like growth factor-IN Longo, R Singh, L D Griffin, et al.
The Journal of Pediatrics|January 1, 1996
A prevalent mutation for galactosemia among black AmericansK Lai, S D Langley, R H Singh, et al.
Transactions of the Association of American Physicians|January 1, 1990
Human fibroblasts express the insulin-responsive glucose transporter (GLUT4)N Longo, G I Bell, R C Shuster, et al.
American Journal of Human Genetics|March 1, 1995
Identification and functional analysis of three distinct mutations in the human galactose-1-phosphate uridyltransferase gene associated with galactosemia in a single familyJ L Fridovich-Keil, S D Langley, L A Mazur, et al.
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