S. Langley

发表

Impaired growth in Rabson-Mendenhall syndrome: lack of effect of growth hormone and insulin-like growth factor-I.

L. Elsas, J. Parks, N. Longo, 1994, The Journal of clinical endocrinology and metabolism.

Molecular genetics of severe insulin resistance.

L. Elsas, N. Longo, L. Griffin, 1989, The Yale journal of biology and medicine.

Urine and plasma galactitol in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia.

S. Wehrli, L. Elsas, R. Singh, 1999, Metabolism: clinical and experimental.

Streptococcus mutans adherence: presumptive evidence for protein-mediated attachment followed by glucan-dependent cellular accumulation.

S. Langley, R. Doyle, R. H. Staat, 1980, Infection and immunity.

Role of arginine 86 of the insulin receptor in insulin binding and activation of glucose transport.

N. Longo, S. Langley, M. Still, 1998, Biochimica et biophysica acta.

Increased glucose transport by human fibroblasts with a heritable defect in insulin binding.

L. Elsas, N. Longo, L. Griffin, 1989, Metabolism: clinical and experimental.

Reduced mRNA and a nonsense mutation in the insulin-receptor gene produce heritable severe insulin resistance.

L. Elsas, N. Longo, L. Griffin, 1992, American journal of human genetics.

Galactosemia: a strategy to identify new biochemical phenotypes and molecular genotypes.

P. Fernhoff, J. Fridovich-Keil, L. Elsas, 1995, American journal of human genetics.

A common mutation associated with the Duarte galactosemia allele.

J. Fridovich-Keil, L. Elsas, S. Langley, 1994, American journal of human genetics.

Genotype-phenotype correlation in inherited severe insulin resistance.

L. Dimeglio, N. Longo, S. Langley, 2002, Human molecular genetics.

Human fibroblasts express the insulin-responsive glucose transporter (GLUT4).

L. Elsas, G. Bell, N. Longo, 1990, Transactions of the Association of American Physicians.

Activation of insulin receptor signaling by a single amino acid substitution in the transmembrane domain.

L. Elsas, N. Longo, L. Griffin, 1992, The Journal of biological chemistry.

Molybdoenzymes in Drosophila. IV. Further characterization of the cinnamon phenotype

S. Langley, V. Finnerty, C. Warner, 1988, Molecular and General Genetics MGG.

GALT deficiency causes UDP-hexose deficit in human galactosemic cells.

L. Elsas, S. Langley, K Lai, 2003, Glycobiology.

A molecular approach to galactosemia

L. Elsas, S. Langley, P. Dembure, 2005, European Journal of Pediatrics.

Characterization of a carbohydrate response element regulating the gene for human galactose-1-phosphate uridyltransferase.

L. Elsas, S. Langley, A. L. Webb, 2002, Molecular genetics and metabolism.

Functional analysis of the human galactose-1-phosphate uridyltransferase promoter in Duarte and LA variant galactosemia.

Carol J. Saunders, C. Saunders, L. Elsas, 2001, Molecular genetics and metabolism.

The Duarte allele impairs biostability of galactose‐1‐phosphate uridyltransferase in human lymphoblasts

L. Elsas, S. Langley, P. Dembure, 1998, Human mutation.

Molecular basis for Duarte and Los Angeles variant galactosemia.

S. Langley, P. Dembure, K. Lai, 1997, American journal of human genetics.

A prevalent mutation for galactosemia among black Americans.

L. Elsas, S. Langley, K. Lai, 1996, The Journal of pediatrics.

Identification and functional analysis of three distinct mutations in the human galactose-1-phosphate uridyltransferase gene associated with galactosemia in a single family.

J. Elsas, J. Fridovich-Keil, S. Langley, 1995, American journal of human genetics.

Two mutations in the insulin receptor gene of a patient with leprechaunism: application to prenatal diagnosis.

L. Elsas, N. Longo, L. Griffin, 1995, The Journal of clinical endocrinology and metabolism.

Prenatal analysis of the insulin receptor gene in a family with leprechaunism

L. Elsas, N. Longo, S. Langley, 1995, Prenatal diagnosis.

Activation of glucose transport by a natural mutation in the human insulin receptor.

L. Elsas, N. Longo, L. Griffin, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Restriction fragment length polymorphisms of the insulin receptor gene in families with insulin resistance and leprechaunism.

L. Elsas, N. Longo, S. Langley, 1989, American Journal of the Medical Sciences.

Glucose transport by cultured human fibroblasts: regulation by phorbol esters and insulin.

L. Elsas, N. Longo, L. Griffin, 1992, Biochimica et biophysica acta.

Mutations in the insulin receptor and their effect on glucose transport.

L. Elsas, N. Longo, L. Griffin, 1992, Transactions of the Association of American Physicians.