Zobrazeno 1 - 10
of 40
pro vyhledávání: '"S H, Black"'
Autor:
M. L. Forister, S. H. Black, C. S. Elphick, E. M. Grames, C. A. Halsch, C. B. Schultz, D. L. Wagner
Publikováno v:
Conservation Letters, Vol 16, Iss 3, Pp n/a-n/a (2023)
Abstract The fate of insects in the Anthropocene has been widely discussed in the scientific literature, the popular media, and in policy circles. This recent attention is justified because reductions in insect abundance and diversity have the potent
Externí odkaz:
https://doaj.org/article/f95086e5a15b4a458063aa0cc2dee741
Publikováno v:
Journal of Medical Virology. 36:21-27
Using a double polymerase chain reaction a method was devised for detecting and subtyping hepatitis B virus DNA in serum samples. Primers from the S-gene were selected from the sequence analyses of five HBV HBsAg subtypes, to amplify HBV DNA and subt
Publikováno v:
Journal of assisted reproduction and genetics. 18(10)
The purpose was to determine whether the number of embryos available for transfer following IVF in women over age 39 predicted a successful pregnancy outcome.Retrospective analysis of 455 consecutive IVF cycles in womenor = 40 years of age.Few cycles
Publikováno v:
Obstetrics and gynecology. 97(2)
To evaluate the clinical outcome of in vitro fertilization (IVF) treatment cycles from individual oocyte donors who underwent multiple sequential donations.We reviewed clinical outcome data from sequential anonymous oocyte donation cycles using donor
Publikováno v:
Prenatal diagnosis. 20(5)
We report three false negative prenatal diagnostic results, using direct measurement of glycine cleavage enzyme activity in uncultured chorionic villus tissue from 290 pregnancies at risk for non-ketotic hyperglycinaemia (NKH). Testing was done by tw
Autor:
W C, Spence, S H, Black, L, Fallon, A, Maddalena, E, Cummings, G, Menapace-Drew, D P, Bick, G, Levinson, J D, Schulman, P N, Howard-Peebles
Publikováno v:
American journal of medical genetics. 64(1)
In December, 1993, we initiated a pilot project in which DNA fragile X (fraX) testing was offered during routine prenatal or genetic counseling to all pregnant women seen at the GeneticsIVF Institute, most of whom were referred for the indication of
Autor:
S L, Christian, A C, Smith, M, Macha, S H, Black, F F, Elder, J M, Johnson, R G, Resta, U, Surti, L, Suslak, M S, Verp, D H, Ledbetter
Publikováno v:
Prenatal diagnosis. 16(4)
Maternal uniparental disomy 15 (UPD15), responsible for approximately 25 per cent of Prader-Willi syndrome cases, is usually caused by maternal meiosis I non-disjunction associated with advanced maternal age. These cases may initially be detected as
Autor:
J. P. Bonnefont, J. D. Schulman, R. J M Gardner, T. L. Kelson, J. M. Saudubray, D. A. Craft, S. H. Black, M. Dirocco, K. Tabsh, William B. Rizzo
Publikováno v:
Prenatal diagnosis. 14(7)
Sjogren—Larsson syndrome (SLS) is an autosomal recessive disorder characterized by the presence of congenital ichthyosis, mental retardation, and spasticity. The primary biochemical defect in SLS has recently been identified to be a deficiency of f
Publikováno v:
Journal of Clinical Pathology. 36:577-580
During each of the four-year periods 1971-1975 and 1975-1979, the annual incidence of hepatitis B infection has been assessed in 56 patients with haemophilia A by measuring plasma HBsAg, anti-HBs and anti-HBc levels. Infection rates of 7% and 9.5% pe
Publikováno v:
Journal of Medical Virology. 3:19-26
HBsAg and anti-HBs can be detected by double-antibody radioimmunoassay in a reliable routine overnight assay of sensitivity approaching that of solid-phase immunoradiometric assay. The test requires careful standardisation and regular preparation of