Literature DB >> 23209180

The influence of genetics on cystic fibrosis phenotypes.

Michael R Knowles1, Mitchell Drumm.   

Abstract

Technological advances in genetics have made feasible and affordable large studies to identify genetic variants that cause or modify a trait. Genetic studies have been carried out to assess variants in candidate genes, as well as polymorphisms throughout the genome, for their associations with heritable clinical outcomes of cystic fibrosis (CF), such as lung disease, meconium ileus, and CF-related diabetes. The candidate gene approach has identified some predicted relationships, while genome-wide surveys have identified several genes that would not have been obvious disease-modifying candidates, such as a methionine sulfoxide transferase gene that influences intestinal obstruction, or a region on chromosome 11 proximate to genes encoding a transcription factor and an apoptosis controller that associates with lung function. These unforeseen associations thus provide novel insight into disease pathophysiology, as well as suggesting new therapeutic strategies for CF.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 23209180      PMCID: PMC3543075          DOI: 10.1101/cshperspect.a009548

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Med        ISSN: 2157-1422            Impact factor:   6.915


  55 in total

1.  Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study.

Authors:  M Gabolde; M Guilloud-Bataille; J Feingold; C Besmond
Journal:  BMJ       Date:  1999-10-30

2.  Liver expression in cystic fibrosis could be modulated by genetic factors different from the cystic fibrosis transmembrane regulator genotype.

Authors:  G Castaldo; A Fuccio; D Salvatore; V Raia; T Santostasi; S Leonardi; N Lizzi; M La Rosa; N Rigillo; F Salvatore
Journal:  Am J Med Genet       Date:  2001-02-01

Review 3.  Genotype-phenotype relationships in cystic fibrosis.

Authors:  J E Mickle; G R Cutting
Journal:  Med Clin North Am       Date:  2000-05       Impact factor: 5.456

4.  Heritability of respiratory infection with Pseudomonas aeruginosa in cystic fibrosis.

Authors:  Deanna M Green; J Michael Collaco; Kathryn E McDougal; Kathleen M Naughton; Scott M Blackman; Garry R Cutting
Journal:  J Pediatr       Date:  2012-02-23       Impact factor: 4.406

Review 5.  Modifier genes in Mendelian disorders: the example of cystic fibrosis.

Authors:  Garry R Cutting
Journal:  Ann N Y Acad Sci       Date:  2010-12       Impact factor: 5.691

6.  EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity.

Authors:  Rebecca Darrah; Edward McKone; Clare O'Connor; Christine Rodgers; Alan Genatossio; Sharon McNamara; Ronald Gibson; J Stuart Elborn; Madeleine Ennis; Charles G Gallagher; Noor Kalsheker; Moira Aitken; Dawn Wiese; John Dunn; Paul Smith; Rhonda Pace; Douglas Londono; Katrina A B Goddard; Michael R Knowles; Mitchell L Drumm
Journal:  Physiol Genomics       Date:  2009-12-22       Impact factor: 3.107

7.  Cytokine-mediated Bax deficiency and consequent delayed neutrophil apoptosis: a general mechanism to accumulate effector cells in inflammation.

Authors:  B Dibbert; M Weber; W H Nikolaizik; P Vogt; M H Schöni; K Blaser; H U Simon
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-09       Impact factor: 11.205

8.  TGF-beta(1) genotype and accelerated decline in lung function of patients with cystic fibrosis.

Authors:  P D Arkwright; S Laurie; M Super; V Pravica; M J Schwarz; A K Webb; I V Hutchinson
Journal:  Thorax       Date:  2000-06       Impact factor: 9.139

9.  Modulation of cystic fibrosis lung disease by variants in interleukin-8.

Authors:  A D Hillian; D Londono; J M Dunn; K A B Goddard; R G Pace; M R Knowles; M L Drumm
Journal:  Genes Immun       Date:  2008-06-19       Impact factor: 2.676

10.  Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia.

Authors:  Frauke Stanke; Tim Becker; Vinod Kumar; Silke Hedtfeld; Christian Becker; Harry Cuppens; Stephanie Tamm; Jennifer Yarden; Ulrike Laabs; Benny Siebert; Luis Fernandez; Milan Macek; Dragica Radojkovic; Manfred Ballmann; Joachim Greipel; Jean-Jacques Cassiman; Thomas F Wienker; Burkhard Tümmler
Journal:  J Med Genet       Date:  2010-09-12       Impact factor: 6.318

View more
  34 in total

1.  TNF-alpha polymorphisms as a potential modifier gene in the cystic fibrosis.

Authors:  Cyntia Aac Coutinho; Fernando Al Marson; Aline Rb Marcelino; Luciana C Bonadia; Marcelo P Carlin; Antonio F Ribeiro; Jose D Ribeiro; Carmen S Bertuzzo
Journal:  Int J Mol Epidemiol Genet       Date:  2014-05-29

2.  The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR Mutations.

Authors:  Pankaj B Agrawal; Ruobing Wang; Hongmei Lisa Li; Klaus Schmitz-Abe; Chantelle Simone-Roach; Jingxin Chen; Jiahai Shi; Tin Louie; Shaohu Sheng; Meghan C Towne; Christine F Brainson; Michael A Matthay; Carla F Kim; Michael Bamshad; Mary J Emond; Norma P Gerard; Thomas R Kleyman; Craig Gerard
Journal:  Am J Respir Cell Mol Biol       Date:  2017-12       Impact factor: 6.914

Review 3.  Cystic fibrosis genetics: from molecular understanding to clinical application.

Authors:  Garry R Cutting
Journal:  Nat Rev Genet       Date:  2014-11-18       Impact factor: 53.242

Review 4.  Cystic fibrosis: a clinical view.

Authors:  Carlo Castellani; Baroukh M Assael
Journal:  Cell Mol Life Sci       Date:  2016-10-05       Impact factor: 9.261

5.  Strong toll-like receptor responses in cystic fibrosis patients are associated with higher lung function.

Authors:  Susanna Kosamo; Katherine B Hisert; Victoria Dmyterko; Catherine Nguyen; R Anthony Black; Tarah D Holden; Frank Radella; Pauline A Cotten; Christopher H Goss; Moira L Aitken; Mark M Wurfel
Journal:  J Cyst Fibros       Date:  2019-12-05       Impact factor: 5.482

6.  Meconium ileus in cystic fibrosis is not linked to central repetitive region length variation in MUC1, MUC2, and MUC5AC.

Authors:  XueLiang Guo; Rhonda G Pace; Jaclyn R Stonebraker; Wanda K O'Neal; Michael R Knowles
Journal:  J Cyst Fibros       Date:  2014-06-08       Impact factor: 5.482

7.  Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable Expressivity.

Authors:  Karen S Raraigh; Sangwoo T Han; Emily Davis; Taylor A Evans; Matthew J Pellicore; Allison F McCague; Anya T Joynt; Zhongzhou Lu; Melis Atalar; Neeraj Sharma; Molly B Sheridan; Patrick R Sosnay; Garry R Cutting
Journal:  Am J Hum Genet       Date:  2018-05-24       Impact factor: 11.025

Review 8.  The Evolution of Cystic Fibrosis Care.

Authors:  Jessica E Pittman; Thomas W Ferkol
Journal:  Chest       Date:  2015-08       Impact factor: 9.410

9.  Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A.

Authors:  Thomas von Kanel; Frauke Stanke; Melanie Weber; Andre Schaller; Julien Racine; Richard Kraemer; Marc Chanson; Burkhard Tümmler; Sabina Gallati
Journal:  Eur J Hum Genet       Date:  2013-04-10       Impact factor: 4.246

Review 10.  The cystic fibrosis intestine.

Authors:  Robert C De Lisle; Drucy Borowitz
Journal:  Cold Spring Harb Perspect Med       Date:  2013-09-01       Impact factor: 6.915

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.