نتایج جستجو برای: heterozygote

تعداد نتایج: 22757  

Journal: :Middle East journal of anaesthesiology 2015
Anis Baraka

Because the parturient should be always considered as a patient with a full stomach and a possible difficult airway, succinylcholine is considered the muscle relaxant of choice for rapid sequence induction of general anesthesia. During pregnancy, the level of plasma cholinesterase which hydrolyses succinylcholine is moderately decreased, and hence hydrolysis of succinylcholine remains within th...

Journal: :Genetics 1988
A Hastings

Equilibrium behavior of two-locus mutation-selection balance models is analyzed using perturbation techniques. The classical result of Haldane for one locus is shown to carry over to two loci, if fitnesses are replaced by marginal fitnesses. If the fitness of the double heterozygote is smaller than would be produced by a multiplicative model, as in additive or quantitative fitness models, the d...

Journal: :Medical and veterinary entomology 1999
P Solano S de La Rocque D Cuisance B Geoffroy T De Meeus G Cuny G DuVallet

Glossina palpalis gambiensis Vanderplank (Diptera: Glossinidae) from West Africa (Senegal and Burkina Faso) were analysed for microsatellite DNA polymorphisms and size of the wings. In the overall sample a strong heterozygote deficiency was found at two polymorphic microsatellite loci. It led to a highly significant value of Fis (within-sample heterozygote deficit) in the western zone of Sidera...

Journal: :Human molecular genetics 2002
David J Kwiatkowski Hongbing Zhang Jennifer L Bandura Kristina M Heiberger Michael Glogauer Nisreen el-Hashemite Hiroaki Onda

Tuberous sclerosis (TSC) is a autosomal dominant genetic disorder caused by mutations in either TSC1 or TSC2, and characterized by benign hamartoma growth. We developed a murine model of Tsc1 disease by gene targeting. Tsc1 null embryos die at mid-gestation from a failure of liver development. Tsc1 heterozygotes develop kidney cystadenomas and liver hemangiomas at high frequency, but the incide...

2008
MASOUD SHEIDAI

Acytogenetic study was performed on 66 tetraploid cotton cultivars (Gossypium hirsutum L.) and their hybrids. The cultivars studied differed significantly in their chiasma frequency and distribution as well as chromosome pairing indicating their genetic differences. Adjacent and alternate quadrivalents were formed in most of the cultivars. A-A or D-D heterozygote translocations occurred in most...

Journal: :Genetics 1975
C Wills

A reanalysis of Drosophila viability data was undertaken to determine the role of genotype-environment interactions in the maintenance of polymorphism. Between-replicate variances of viabilities in chromosomal homozygotes and heterozygotes with the same mean fitnesses were compared, with the expectation that if the heterozygote variance were on the average greater, conditional overdominance wou...

2017
Zahra Heydarifard Alijan Tabarraei Abdolvahab Moradi

Prevalence of CCR5Δ32 among blood samples of more than 400 healthy and HIV-1-infected people was investigated in Iran. Polymerase chain reaction (PCR) following DNA extraction was used. Desired frequency was analyzed by Hardy-Weinberg equilibrium (HWE) analysis and SPSS 16.0 software to harvest the results. The prevalence of CCRΔ32 heterozygote genotype was 3% in healthy people and 0.7% in HIV-...

Journal: :Prilozi 2015
Zoran Gucev Velibor Tasic

Krabbe disease (KD) (globoid cell leukodystrophy) is a degenerative, lysosomal storage disease, caused by a severe loss of galactocerebrosidase (GALC) enzymatic activity. The inheritance is autosomal recessive. KD affects the white matter of the central and peripheral nervous systems. We present a 3 year old boy in whom the disease had an 'infantile' or 'classic' presentation, with spasticity, ...

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