نتایج جستجو برای: heterozygotes

تعداد نتایج: 4125  

Journal: :Proteomics. Clinical applications 2014
Stefan Ljunggren Johannes H M Levels Maria V Turkina Sofie Sundberg Andrea E Bochem Kees Hovingh Adriaan G Holleboom Mats Lindahl Jan Albert Kuivenhoven Helen Karlsson

PURPOSE Mutations in apolipoprotein A-I (apoA-I) may affect plasma high-density lipoprotein (HDL) cholesterol levels and the risk for cardiovascular disease but little is known about the presence and effects of circulating apoA-I variants. This study investigates whether the apoA-I mutations, apoA-I(L202P) and apoA-I(K131del) , are present on plasma HDL particles derived from heterozygote carri...

Journal: :American journal of hematology 1989
M Lakomek H Winkler S Linne W Schröter

The goal of the present study was to search for criteria that allow one to distinguish between normal individuals and heterozygotes as well as compound heterozygotes for pyruvate kinase (PK) deficiency. As the residual activity of PK with heterozygotes was between 35% and 110% of the normal activity, it was necessary to find other methods to prove heterozygosity. The PK in the hemolysates of 23...

Journal: :The Journal of clinical investigation 2000
S M Clee J J Kastelein M van Dam M Marcil K Roomp K Y Zwarts J A Collins R Roelants N Tamasawa T Stulc T Suda R Ceska B Boucher C Rondeau C DeSouich A Brooks-Wilson H O Molhuizen J Frohlich J Genest M R Hayden

We and others have recently identified mutations in the ABCA1 gene as the underlying cause of Tangier disease (TD) and of a dominantly inherited form of familial hypoalphalipoproteinemia (FHA) associated with reduced cholesterol efflux. We have now identified 13 ABCA1 mutations in 11 families (five TD, six FHA) and have examined the phenotypes of 77 individuals heterozygous for mutations in the...

2009
Gudlaug Tórsdóttir Grétar Gudmundsson Jakob Kristinsson Jón Snaedal Torkell Jóhannesson

At the time of this study, there were five known patients with Wilson disease (WD) in Iceland. The mutation, a 7-bp deletion in exon 7 on chromosome 13 for WD, is only known in Iceland. In twenty healthy Icelandic heterozygotes for WD and their age- and gender-matched controls, copper concentration in plasma, ceruloplasmin (CP) concentration, CP oxidative activity and CP-specific oxidative acti...

2005
William K. Dahlberg John B. Little

We examined the cytotoxic effects of radiation delivered in daily fractions at clinically relevant doses in plateau phase cultures of skin fibroblast cell strains derived from ataxia telangiectasia (AT) heterozygotes, patients with unusually sensitive responses to radiotherapy, apparently normal patients, and cell bank controls. A gradual linear reduction in surviving fraction versus total dose...

Journal: :The European respiratory journal 2012
M Thomsen B G Nordestgaard A A Sethi A Tybjærg-Hansen M Dahl

The β(2)-adrenergic receptor (ADRB2) is an important regulator of airway smooth muscle tone. We tested the hypothesis that three functional polymorphisms in the ADRB2 gene (Thr164Ile, Gly16Arg and Gln27Glu) are associated with reduced lung function, asthma or chronic obstructive pulmonary disease (COPD). We first genotyped 8,971 individuals from the Copenhagen City Heart Study for all three pol...

Journal: :The Malaysian journal of pathology 2012
Alauddin Hafiza Mohd Yusoff Malisa R D Aidifitrina Khirotdin Ithnin Azlin Zahratul Azma Matthew Chong Kwok Thong Irwan Mohamad Ali Zi-Ning Yeoh Lailyvia Mohd Ishak Nur Rabiatuladawiah Mohd Radzi Noor Hamidah Hussin

OBJECTIVE The capillary electrophoresis (CE) is a new system that utilizes the principle of electrokinetic separation of molecules in eight electrolyte buffer-filled silica capillaries. In this study, we established the normal ranges of haemoglobin A2 (HbA2) and haemoglobin F (HbF) levels for normal individuals using this system and also the HbA2 level in beta thalassaemia and haemoglobin E (Hb...

2010
David J. Speca Daisuke Chihara Amir M. Ashique M. Scott Bowers Jonathan T. Pierce-Shimomura Jungsoo Lee Nusrat Rabbee Terence P. Speed Rodrigo J. Gularte James Chitwood Juan F. Medrano Mark Liao James M. Sonner Edmond I. Eger Andrew S. Peterson Steven L. McIntire

The mechanisms by which ethanol and inhaled anesthetics influence the nervous system are poorly understood. Here we describe the positional cloning and characterization of a new mouse mutation isolated in an N-ethyl-N-nitrosourea (ENU) forward mutagenesis screen for animals with enhanced locomotor activity. This allele, Lightweight (Lwt), disrupts the homolog of the Caenorhabditis elegans (C. e...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1995
W K DahlBerg J B Little

We examined the cytotoxic effects of radiation delivered in daily fractions at clinically relevant doses in plateau phase cultures of skin fibroblast cell strains derived from ataxia telangiectasia (AT) heterozygotes, patients with unusually sensitive responses to radiotherapy, apparently normal patients, and cell bank controls. A gradual linear reduction in surviving fraction versus total dose...

Journal: :Clinical chemistry 2001
E Rossi M K Bulsara J K Olynyk D J Cullen L Summerville L W Powell

BACKGROUND Heterozygotes for the C282Y mutation of the HFE gene may have altered hematology indices and higher iron stores than wild-type subjects. METHODS We performed a cross-sectional analysis of 1488 females and 1522 males 20-79 years of age drawn from the Busselton (Australia) population study to assess the effects of HFE genotype, age, gender, and lifestyle on serum iron and hematology ...

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