Zobrazeno 1 - 10
of 27
pro vyhledávání: '"D R, Love"'
Publikováno v:
Acta Anaesthesiologica Scandinavica. 42:527-531
Background: This study examined the influence of premedication with morphine or diazepam on the dose of eltanolone, a steroidal intravenous anaesthetic agent, required to induce anaesthesia. Methods: Two hundred and sixteen patients, aged 18 to 65 ye
Publikováno v:
Internal medicine journal. 43(4)
Phaeochromocytomas and paragangliomas are rare neuroendocrine tumours that arise from the adrenal glands or paraganglia (paragangliomas) within the abdomen, thorax and neck. Although it was originally suggested that approximately 10% of these tumours
Publikováno v:
Genetics and molecular research : GMR. 10(3)
Replacement of endogenous genes by homologous recombination is rare in plants; the majority of genetic modifications are the result of transforming DNA molecules undergoing random genomic insertion by way of non-homologous recombination. Factors that
Publikováno v:
Methods in cell biology. 105
Zebrafish have proved to be a popular species for the modeling of human disease. In this context, there is a need to move beyond chemical-based mutagenesis and develop tools that target genes that are orthologous to those that are implicated in human
Publikováno v:
Singapore medical journal. 52(7)
A five-year-old girl with global developmental delay and mild dysmorphic features was referred for karyotyping. Cytogenetic analysis identified an interstitial deletion in the approximate position of chromosome band 10q23.1. The patient's DNA was ana
Publikováno v:
Genetics and molecular research : GMR. 9(3)
Sex reversal due to duplication of the Xp21 dosage-sensitive sex reversal locus results in XY females with gonadal dysgenesis. Pure Xp disomy (without a concurrent loss of genetic material) can occur by translocation or interstitial duplication. The
Publikováno v:
Genetics and molecular research : GMR. 9(3)
We developed a mutation-screening protocol for the ASS1 gene in order to guide clinical management of neonates with elevated citrulline detected during routine newborn screening. An exon-based amplification and sequencing method was designed and succ
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 99(5)
13q deletion is a rare cause of ambiguous genitalia in the male newborn, and can be associated with mental retardation of varying degree, retinoblastoma, and malformations of the brain, eye, genitourinary and gastrointestinal tract, depending on the
Publikováno v:
Methods in cell biology. 77
Autor:
D R, Love
Publikováno v:
Clinical genetics. 65(1)