L. A. Clarke

发表

Alternative splicing of the prolactin receptor gene generates a 1.7 kb RNA transcript that is linked to prolactin function in the red deer testis.

P. Kelly, M. Edery, H. Jabbour, 1998, Journal of molecular endocrinology.

Expression and localization of prolactin receptor messenger ribonucleic acid in red deer ovary during the estrous cycle and pregnancy.

H. Jabbour, D. Wathes, L. A. Clarke, 1997, Biology of reproduction.

Cloning, sequencing and functional analysis of a truncated cDNA encoding red deer prolactin receptor: an alternative tyrosine residue mediates β-casein promoter activation

P. Kelly, M. Edery, H. Jabbour, 1996, Molecular and Cellular Endocrinology.

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

E. Haan, R. Markowitz, A. Guttmacher, 1997, American journal of human genetics.

T cell activation profiles in Kawasaki syndrome

N. Klein, P. Brogan, V. Shah, 2007, Clinical and experimental immunology.

Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome.

W. Seltzer, D. Cole, S. Salisbury, 1994, Clinical chemistry.

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

E. Zackai, M. Muenke, G. Bellus, 1996, Nature Genetics.

Is prolactin a gonadotrophic hormone in red deer (Cervus elaphus)? Pattern of expression of the prolactin receptor gene in the testis and epididymis.

P. Kelly, M. Edery, H. Jabbour, 1998, Journal of molecular endocrinology.

Expression of the prolactin receptor gene during the breeding and non-breeding seasons in red deer (Cervus elaphus): evidence for the expression of two forms in the testis.

A. Loudon, P. Kelly, M. Edery, 1995, The Journal of endocrinology.

Associative learning, short-term memory, and colour preference during first feeding by juvenile Atlantic salmon

A. Sutterlin, L. A. Clarke, 1985 .

Isolated mitochondria from frozen muscle have limited value in diagnostics

D. Applegarth, H. Scholte, J. Trijbels, 2005, European Journal of Pediatrics.

Molecular genetics of muccpolysaccharidosis type I: Diagnostic, clinical, and biological implications

H. Scott, J. Hopwood, A. Gal, 1995 .

Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

C. P. Morris, H. Scott, J. Hopwood, 1995, Human mutation.

A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians.

M. Hayden, P. Julien, J. Brunzell, 1991, The New England journal of medicine.

Murine MPS I: insights into the pathogenesis of Hurler syndrome

K. Ng, L. Clarke, G. Hendson, 1998, Clinical genetics.

Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity.

E. Zackai, J. Allanson, N. Robin, 1994, Human molecular genetics.

Stability of frozen muscle used for mitochondrial enzyme assays

D. Applegarth, T. Tong, L. A. Clarke, 1994, European Journal of Pediatrics.