Zobrazeno 1 - 10
of 201
pro vyhledávání: '"N.D. Carter"'
Autor:
H. Moattar, G. Foteinos, K. Mandel, B. Zal, A. Weerasinghe, S. Fredricks, M. Jahangiri, N.D. Carter, A. Afzal
Publikováno v:
Artery Research, Vol 1, Iss 1 (2007)
Externí odkaz:
https://doaj.org/article/c3bf897bb1b64ced94bdb3bc59085b0d
Carbonic anhydrase (CA) is a seemingly ubiquitous enzyme of profound physiological importance, which plays essential roles in respiration, acid-base homeostasis, bone resorption, calcification, photosynthesis, several biosynthetic pathways and a vari
As we approach the twenty-first century the problems of industrialization are evident: we find there is a greenhouse effect, the ozone layer is being depleted, the rain is acidified, and there is a terrible problem of increasing C0 concentrations in
Publikováno v:
Medical and Pediatric Oncology. 36:142-146
Background Endothelins and their receptors, Et-A and Et-B, play an essential role in differentiation and migration of neural crest cells. Expression of endothelin receptors has been examined in neuroblastoma and Ewing sarcoma cell lines. Procedure RN
Publikováno v:
Journal of neuroendocrinology. 2(4)
The possibility that steroids exert their effects on luteinizing hormone (LH) and prolactin release and female sexual behaviour via altering gamma-aminobutyric acid (GABA) synthesis within the hypothalamus was investigated. Ovariectomized rats were t
Autor:
M. Jahangiri, G. Foteinos, H. Moattar, N.D. Carter, S. Fredricks, K. Mandel, B. Zal, A. Weerasinghe, A. Afzal
Publikováno v:
Artery Research, Vol 1, Iss 1 (2007)
Autor:
R. G. Huntsman, D.J. Aidley, N.D. Carter, R.B. Powell, C.W. Parr, B.J. Culliford, G.C. Jenkins, J.V. Barry, S.G. Welch
Publikováno v:
Human Heredity. 25:346-353
161 inhabitants of the Seychelle Islands have been examined for blood group, serum protein, and red cell enzyme polymorphisms. The gene frequency data obtained from this survey supports the anthropological view that the present-day Creole-speaking in
Publikováno v:
Human Heredity. 25:13-17
Electrophoresis of haemolysates from a population in London resulted in the detection of a variant of haemoglobin-A2. Purification and characterisation of the variant globin revealed that t
Publikováno v:
Human Heredity. 26:4-7
An electrophoretic survey of variant red cell enzyme phenotypes in an isolated community in Newfoundland gave gene frequencies in marked contrast to those found in the capital, St. John's. In particular, a variant of red cell superoxide dismutase (SO
Autor:
A. Warlow, M. Lahav, H. Sørensen, N.D. Carter, G. Tusnady, J. Dissing, C. Ropartz, L.C. Legueult, I. Persson, K. Ohkura, L. Rivat, G. Beckman, K. Berg, H. Gershowitz, M.S. Adams, T.M. Allan, N. Myrberg, A. Pellicer, D.P. Agarwal, V. Bhalla, James J. Nora, S. Singh, J. Lund, G. Berlin, H.R. Maricq, K. Kølendorf, Anil K. Sinha, L. Beckman, Luan Eng Lie-Injo, Liliane Rivat, S.S. Magnússon, S. Ashbel, L. Kølendorf, L.R. Weitkamp, P.H. Alsbirk, A.W. Eriksson, P.T. Rowley, E. Monn, M.S. Schanfield, B. Sela, B. Bonné, Benkmann Hg, H. Walter, A. Szeinberg, H.-G. Benkmann, K.E. Alsbirk, Q.B. Welch, A. Czeizel, A.R. Coward, L. Hirth, Sen Pathak, Hazel Camoens, A.E. Mourant, C.J. Brackenridge, T. Pellicer, T.E.B. Leakey, P.Y. Rousseau, H. Arvilommi, R. Ananthakrishnan, M. Stahn, H.W. Goedde, L. Tsacheva
Publikováno v:
Human Heredity. 22:I-VIII