نتایج جستجو برای: heterozygote

تعداد نتایج: 22757  

2014
Min Lin Ji-Wei Jiao Xiu-Hui Zhan Xiao-Fen Zhan Mei-Chen Pan Jun-Li Wang Chun-Fang Wang Tian-Yu Zhong Qin Zhang Xia Yu Jiao-Ren Wu Hui-Tian Yang Fen Lin Xin Tong Hui Yang Guang-Cai Zha Qian Wang Lei Zheng Ying-Fang Wen Li-Ye Yang

β-thalassemia is a common inherited disorder worldwide including southern China, and at least 45 distinct β-thalassemia mutations have been identified in China. High-resolution melting (HRM) assay was recently introduced as a rapid, inexpensive and effective method for genotyping. However, there was no systemic study on the diagnostic capability of HRM to identify β-thalassemia. Here, we used a...

2003
S Campbell H J Dargie P R Mills

Objectives: Excess iron stores have been postulated to enhance the risk of ischaemic heart disease. This study aims to determine whether the two major mutations of the haemochromatosis (HFE) gene (C282Y and H63D) are associated with ischaemic heart disease (IHD) or myocardial infarction (MI). Design: Cross sectional case–control study. Setting: The geographical area studied by the MONICA (monit...

Journal: :Heart 2003
S Campbell D K George S D Robb R Spooner T A McDonagh H J Dargie P R Mills

OBJECTIVES Excess iron stores have been postulated to enhance the risk of ischaemic heart disease. This study aims to determine whether the two major mutations of the haemochromatosis (HFE) gene (C282Y and H63D) are associated with ischaemic heart disease (IHD) or myocardial infarction (MI). DESIGN Cross sectional case-control study. SETTING The geographical area studied by the MONICA (moni...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005
Mobin M Siddique Chowbay Balram Lucja Fiszer-Maliszewska Amit Aggarwal Angie Tan Patrick Tan Khee C Soo Kanaga Sabapathy

Polymorphism at codon 72 of p53 results in either the arginine or proline form of p53, whose functional significance in carcinogenesis is controversial. We have investigated if the expression of these p53 polymorphs is selectively regulated, using mRNA from peripheral blood of healthy Asian (Chinese) and the Caucasian (Polish) arginine/proline (arg/pro) heterozygote subjects. Asians were found ...

Journal: :Clinical science 1988
C J Danpure P R Jennings

1. The activity of alanine:glyoxylate aminotransferase (AGT; EC 2.6.1.44) has been measured in the unfractionated livers of 20 patients with primary hyperoxaluria type 1 (PH1), three patients with other forms of primary hyperoxaluria and one PH1 heterozygote. The subcellular distribution of AGT activity was examined in four of the PH1 livers and in the liver of the PH1 heterozygote. 2. The mean...

Journal: :Genetics 1992
D B Goldstein

The life cycle of eukaryotic, sexual species is divided into haploid and diploid phases. In multicellular animals and seed plants, the diploid phase is dominant, and the haploid phase is reduced to one, or a very few cells, which are dependent on the diploid form. In other eukaryotic species, however, the haploid phase may dominate or the phases may be equally developed. Even though an alternat...

2005
LUDOVIC SAY FAVEL NAULTY ANTOINETTE FENNELL THOMAS JOSEPH HAYDEN T. J. Hayden

Effects of inbreeding on individual fitness are of long-standing interest in evolutionary biology and conservation studies. Since estimation of the inbreeding coefficient of a given individual is often impossible in wild populations, some authors have attempted to demonstrate inbreeding depression in such populations by correlating the multi-locus marker heterozygosity of individuals with a tra...

2012
Gary Mockli

In 1887, Bernard Sachs reported on the clinical features diagnostic signs and symptoms and pathology of a patient with a condition that would someday bear his name(l). It was several decades later before it was discovered that these patients suffered from a recessive genetic trait resulting in the accumulation of a specific ganglioside, GM2, due to the deficiency of the lysosomal enzyme hexosam...

Journal: :Journal of Medical Genetics 1971

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