Literature DB >> 9708232

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

D J Davidson1, D J Porteous.   

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Year:  1998        PMID: 9708232      PMCID: PMC1745224          DOI: 10.1136/thx.53.5.389

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


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  38 in total

1.  Pathology of cystic fibrosis review of the literature and comparison with 146 autopsied cases.

Authors:  E H Oppenheimer; J R Esterly
Journal:  Perspect Pediatr Pathol       Date:  1975

2.  Mucociliary transport in trachea of patients with cystic fibrosis.

Authors:  D B Yeates; J M Sturgess; S R Kahn; H Levison; N Aspin
Journal:  Arch Dis Child       Date:  1976-01       Impact factor: 3.791

3.  A peptide antibiotic from human skin.

Authors:  J Harder; J Bartels; E Christophers; J M Schröder
Journal:  Nature       Date:  1997-06-26       Impact factor: 49.962

4.  A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction.

Authors:  J R Dorin; R Farley; S Webb; S N Smith; E Farini; S J Delaney; B J Wainwright; E W Alton; D J Porteous
Journal:  Gene Ther       Date:  1996-09       Impact factor: 5.250

Review 5.  New pharmaceutical approaches to the treatment of cystic fibrosis.

Authors:  S J Delaney; B J Wainwright
Journal:  Nat Med       Date:  1996-04       Impact factor: 53.440

Review 6.  Towards an ovine model of cystic fibrosis.

Authors:  A Harris
Journal:  Hum Mol Genet       Date:  1997-12       Impact factor: 6.150

7.  Defective acidification of intracellular organelles in cystic fibrosis.

Authors:  J Barasch; B Kiss; A Prince; L Saiman; D Gruenert; Q al-Awqati
Journal:  Nature       Date:  1991-07-04       Impact factor: 49.962

8.  Early alterations in airway mucociliary clearance and inflammation of the lamina propria in CF mice.

Authors:  J M Zahm; D Gaillard; F Dupuit; J Hinnrasky; D Porteous; J R Dorin; E Puchelle
Journal:  Am J Physiol       Date:  1997-03

9.  Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis.

Authors:  C S Chu; B C Trapnell; S M Curristin; G R Cutting; R G Crystal
Journal:  J Clin Invest       Date:  1992-09       Impact factor: 14.808

10.  Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator.

Authors:  T P Carroll; M M Morales; S B Fulmer; S S Allen; T R Flotte; G R Cutting; W B Guggino
Journal:  J Biol Chem       Date:  1995-05-19       Impact factor: 5.157

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  7 in total

Review 1.  Genetics and pulmonary medicine 8: asthma.

Authors:  I P Hall
Journal:  Thorax       Date:  1999-01       Impact factor: 9.139

Review 2.  Cystic Fibrosis and Pseudomonas aeruginosa: the Host-Microbe Interface.

Authors:  Sankalp Malhotra; Don Hayes; Daniel J Wozniak
Journal:  Clin Microbiol Rev       Date:  2019-05-29       Impact factor: 26.132

Review 3.  Prospects for the prevention and control of pseudomonal infection in children with cystic fibrosis.

Authors:  N Høiby
Journal:  Paediatr Drugs       Date:  2000 Nov-Dec       Impact factor: 3.022

Review 4.  What's new in cystic fibrosis? From treating symptoms to correction of the basic defect.

Authors:  Marijke Proesmans; François Vermeulen; Kris De Boeck
Journal:  Eur J Pediatr       Date:  2008-04-04       Impact factor: 3.183

5.  Multidisciplinary approach to patients with manifestations and pulmonary complications of cystic fibrosis.

Authors:  Viorel Biciuşcă; Ileana Octavia Petrescu; Cristina Elena Singer; Anca Gabriela Oancea; Ana Maria Petrescu; Ionelia Sorina Stan; Patricia Durand; Citto Iulian Taisescu; Daniela Dumitrescu; Mihaela Amelia Dobrescu; Ion Udriştoiu; Diana Rodica Tudoraşcu; Florin Petrescu
Journal:  Rom J Morphol Embryol       Date:  2020 Apr-Jun       Impact factor: 1.033

6.  Bone Mineral Density in Cystic Fibrosis Patients with the CFTR I1234V Mutation in a Large Kindred Family Is Associated with Pancreatic Sufficiency.

Authors:  Atqah Abdul Wahab; M Hammoudeh; Mona Allangawi; Fawziya Al-Khalaf; Prem Chandra
Journal:  Int J Rheumatol       Date:  2014-06-30

7.  Pseudomonas aeruginosa polysaccharide Psl supports airway microbial community development.

Authors:  Sara N Stoner; Joshua J Baty; Jessica A Scoffield
Journal:  ISME J       Date:  2022-03-25       Impact factor: 11.217

  7 in total

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