Literature DB >> 10923221

The geographic distribution of cystic fibrosis mutations gives clues about population origins.

K P Dawson1, P M Frossard.   

Abstract

UNLABELLED: Information regarding three of the more common cystic fibrosis mutations is presented (delta F508, G542X, N13031K) to support the concept of a geography associated with cystic fibrosis mutations. We present the hypothesis that a knowledge of the geography of cystic fibrosis mutations is important for an understanding of genotype-phenotype correlations, gene flow, historical population migration and cystic fibrosis screening.
CONCLUSION: A new method of study of mankind's cultural spread is being revealed and the survival of the various mutations supports the concept that they may provide a selective advantage to the carrier.

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Year:  2000        PMID: 10923221     DOI: 10.1007/s004310051317

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  7 in total

1.  A haplotype framework for cystic fibrosis mutations in Iran.

Authors:  Elahe Elahi; Ahmad Khodadad; Ilya Kupershmidt; Fereshteh Ghasemi; Babak Alinasab; Ramin Naghizadeh; Robert G Eason; Mahshid Amini; Mehran Esmaili; Mohammad R Esmaeili Dooki; Mohammad H Sanati; Ronald W Davis; Mostafa Ronaghi; Yvonne R Thorstenson
Journal:  J Mol Diagn       Date:  2006-02       Impact factor: 5.568

2.  Detecting Common CFTR Mutations by Reverse Dot Blot Hybridization Method in Cystic Fibrosis First Report from Northern Iran.

Authors:  Mohammad-Reza Esmaeili Dooki; Haleh Akhavan-Niaki; Ali Ghabeli Juibary
Journal:  Iran J Pediatr       Date:  2011-03       Impact factor: 0.364

3.  CFTR Mutation Analysis in Western Iran: Identification of Two Novel Mutations.

Authors:  Nasibeh Karimi; Reza Alibakhshi; Shekoufeh Almasi
Journal:  J Reprod Infertil       Date:  2018 Jan-Mar

4.  Liver Failure in a Chinese Cystic Fibrosis Child With Homozygous R553X Mutation.

Authors:  Haiyan Li; Li Lin; Xiaoguang Hu; Changchong Li; Hailin Zhang
Journal:  Front Pediatr       Date:  2019-02-20       Impact factor: 3.418

5.  Reappraisal of Frequency of Common Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Iranian Cystic Fibrosis Patients.

Authors:  Soheila Khalilzadeh; Maryam Hassanzad; Mihan PourAbdollah Toutkaboni; Sabereh Tashayoie Nejad; Fatemeh-Maryam Sheikholeslami; Ali Akbar Velayati
Journal:  Tanaffos       Date:  2018-02

6.  Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran.

Authors:  Atieh Mehdizadeh Hakkak; Mohammad Keramatipour; Saeid Talebi; Azam Brook; Jalil Tavakol Afshari; Amin Raazi; Hamid Reza Kianifar
Journal:  Iran J Basic Med Sci       Date:  2013-08       Impact factor: 2.699

7.  Mutation Analysis of Exons 10 and 17a of CFTR Gene in Patients with Cystic Fibrosis in Kermanshah Province, Western Iran.

Authors:  Abbas Sahami; Reza Alibakhshi; Keyghobad Ghadiri; Hamid Sadeghi
Journal:  J Reprod Infertil       Date:  2014-01
  7 in total

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