Microarray analysis in cystic fibrosis

Author:

Galvin Paul,Clarke Luka A.,Harvey Sara,Amaral Margarida D.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference26 articles.

1. The sequence of the human genome;Venter;Science,2001

2. Genomics, gene expression and DNA arrays;Lockhart;Nature,2000

3. Arrayed primer extension on the DNA chip—method and applications;Tõnisson,2000

4. Cystic fibrosis mutation database. Hospital for Sick Children, Toronto, www.genet.sickkids.on.ca.

5. Cystic fibrosis: a worldwide analysis of CFTR mutations—correlation with incidence data and application to screening;Bobadilla;Hum. Mutat.,2002

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1. Using the genome to correct the ion transport defect in cystic fibrosis;The Journal of Physiology;2022-09-30

2. SWATH label-free proteomics for cystic fibrosis research;Journal of Cystic Fibrosis;2019-07

3. The chloride anion as a signalling effector;Biological Reviews;2019-06-23

4. Extracellular pH and lung infections in cystic fibrosis;European Journal of Cell Biology;2018-08

5. CFTR modulates RPS27 gene expression using chloride anion as signaling effector;Archives of Biochemistry and Biophysics;2017-11

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