Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Judith J. Britten"'
Autor:
Mary Whittaker, Judith J. Britten
Publikováno v:
Human Heredity. 39:1-6
Four families are reported in which the E1j gene is segregating. Two E1j E1k and one E1j E1f
Autor:
Judith J. Britten, Mary Whittaker
Publikováno v:
British Journal of Anaesthesia. 53:241-244
One hundred and six individuals from 33 families with a history of malignant hyperthermia have been investigated for plasma cholinesterase variants. An increased frequency of the fluoride-resistant gene has been found. Although an adequate explanatio
Autor:
Mary Whittaker, Judith J. Britten
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 18:9-14
Five differential inhibitors of plasma cholinesterase have been compared using benzoylcholine as substrate. None of the inhibitors (dibucaine, NaF, NaBr, NaCl, or pancuronium dibutyryloxy bromide) could be used singly to resolve all the variants. Bet
Autor:
Judith J. Britten, Mary Whittaker
Publikováno v:
Human Heredity. 35:364-368
The use of RO2-0683 as differential inhibitor has shown that 13 % of 181 heterozygotes, believed to be E1uE1a, are in fact E1aE1k. The results indicate that slightly more than 1% of the British population could be homozygote E1kE1k. Analysis of 47 fa
Autor:
Judith J. Britten, Mary Whittaker
Publikováno v:
Human Heredity. 38:233-239
The first identification of the cholinesterase variants E1kE1k and E1kE1s is reported from a family study. The e
Publikováno v:
Clinica Chimica Acta. 119:107-114
Human erythrocyte acetylcholinesterase and the plasma cholinesterase variants are not only inhibited by propranolol but have been found to show stereospecificity for its isomers. The erythrocyte enzyme has a greater affinity for the l -isomer than ei
Autor:
Mary Whittaker, Judith J. Britten
Publikováno v:
Human Heredity. 37:54-58
Unusual inhibition characteristics in two unrelated suxamethonium-sensitive individuals were indicative of a new allele, E1h, segregating with the E1a gene. Family studies substantiate this hypothesis and three new genotypes are recognised.
Autor:
Mary Whittaker, P.R. Rao, Bernardo Erdtmann, C. Rahuel, Rosa Maria Corbo, Yoshiro Wada, R. Palmarino, R.J. Mitchell, Gérard Lucotte, E. Calzolari, K.B. Gopalam, M. Frain, S. Lavareda de Souza, Cécile Rahuel, D.G. Woodfield, Renato Scacchi, José M. Sala-Trepat, F. Martuzzi Veronesi, Luc Noel, G. Marogna, Ives José Sbalqueiro, Judith J. Britten, K. Sampat Narasimha Char, Kusuki Nishoka, G. Mulas, Rick Johnson, G. Cossu, C.R. Srikumari, Hisashi Yamanaka, A. Stangoni, G. Laconi, Davide Pettener, Paola Lucarelli, Néria A. Maia, J. Rajanikumari, S.A. Fabb, Iglenir J. Cavalli, G.B. Cuccuru, Tsutomu Ohtani, C.J. Lyne, Naoyuki Kamatani, P.L. Clark, M.A. Lyne, Michio Kobayashi, Margarete S. Mattevi, T. Venkateswara Rao, Kiyonobu Mikanagi
Publikováno v:
Human Heredity. 35:I-VI
Publikováno v:
Human Heredity. 38:228-232
Six individuals in three families with a history of suxamethonium sensitivity have been found to have genotype E1k1s. The biochemical data for the recogniti
Autor:
Judith J. Britten, Mary Whittaker
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 108(1)
Pancuronium bromide, a 3,17-diacetoxy-5 alpha-androstane, and three of its analogues, the 17-desoxy, the 3,17-dibutyryloxy and the 16-N-monoquaternary ammonium derivatives have been used as inhibitors of the usual and atypical plasma cholinesterase v