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R D Milner

Showing results (181-190 of 193) with videos related to

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Archives of Disease in Childhood|October 1, 1970
Neonatal hypoglycaemia in infants of diabetic mothers given sulphonylurea drugs in pregnancyM L Kemball, C McIver, R D Milner, et al.
The Journal of Endocrinology|March 1, 1983
Increased thymidine incorporation into fetal rat cartilage in vitro in the presence of human somatomedin, epidermal growth factor and other growth factorsD J Hill, A T Holder, J Seid, et al.
Journal of Molecular Endocrinology|January 1, 1989
Immunological distribution of one form of insulin-like growth factor (IGF)-binding protein and IGF peptides in human fetal tissuesD J Hill, D R Clemmons, S Wilson, et al.
British Journal of Diseases of the Chest|January 1, 1984
Factors affecting the peak expiratory flow rate in childrenR A Primhak, J D Biggins, J N Tsanakas, et al.
Endocrinology|November 1, 1985
Fetal rat myoblasts release both rat somatomedin-C (SM-C)/insulin-like growth factor I (IGF I) and multiplication-stimulating activity in vitro: partial characterization and biological activity of myoblast-derived SM-C/IGF ID J Hill, C J Crace, S P Nissley, et al.
The Journal of Endocrinology|August 1, 1977
Neonatal islet cell transplantation in the diabetic rat: effect on hepatic enzyme activity and glucose homeostasisY Mangnall, A Smythe, D N Slater, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 1998
Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiencyF Pernasetti, R D Milner, A A al Ashwal, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 1, 1994
Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patientM A Berg, R Peoples, L Pérez-Jurado, et al.
Pediatric Research|November 1, 1984
Reduced plasma somatomedin activity and costal cartilage sulfate incorporation activity during experimental growth retardation in the fetal ratF A De Prins, D J Hill, M Fekete, et al.
Journal of Medical Genetics|November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia familiesR A Gibson, D Ford, S Jansen, et al.
Pageof 20

Showing results (181-190 of 193) with videos related to

Sort By:
Pageof 20
Archives of Disease in Childhood|October 1, 1970
Neonatal hypoglycaemia in infants of diabetic mothers given sulphonylurea drugs in pregnancyM L Kemball, C McIver, R D Milner, et al.
The Journal of Endocrinology|March 1, 1983
Increased thymidine incorporation into fetal rat cartilage in vitro in the presence of human somatomedin, epidermal growth factor and other growth factorsD J Hill, A T Holder, J Seid, et al.
Journal of Molecular Endocrinology|January 1, 1989
Immunological distribution of one form of insulin-like growth factor (IGF)-binding protein and IGF peptides in human fetal tissuesD J Hill, D R Clemmons, S Wilson, et al.
British Journal of Diseases of the Chest|January 1, 1984
Factors affecting the peak expiratory flow rate in childrenR A Primhak, J D Biggins, J N Tsanakas, et al.
Endocrinology|November 1, 1985
Fetal rat myoblasts release both rat somatomedin-C (SM-C)/insulin-like growth factor I (IGF I) and multiplication-stimulating activity in vitro: partial characterization and biological activity of myoblast-derived SM-C/IGF ID J Hill, C J Crace, S P Nissley, et al.
The Journal of Endocrinology|August 1, 1977
Neonatal islet cell transplantation in the diabetic rat: effect on hepatic enzyme activity and glucose homeostasisY Mangnall, A Smythe, D N Slater, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 1998
Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiencyF Pernasetti, R D Milner, A A al Ashwal, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 1, 1994
Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patientM A Berg, R Peoples, L Pérez-Jurado, et al.
Pediatric Research|November 1, 1984
Reduced plasma somatomedin activity and costal cartilage sulfate incorporation activity during experimental growth retardation in the fetal ratF A De Prins, D J Hill, M Fekete, et al.
Journal of Medical Genetics|November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia familiesR A Gibson, D Ford, S Jansen, et al.
Pageof 20