(Q36724262)

15 August 2017

title

Probing the basic defect in cystic fibrosis (English)

1 reference

15 August 2017

0 references

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

9 November 2022

author name string

L. C. Tsui

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1726721

9 November 2022

publication date

1 June 1991

1 reference

15 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1726721

https://api.elsevier.com/content/article/PII:0959437X9180032H?httpAccept=text/xml

9 November 2022

work available at URL

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

https://api.elsevier.com/content/article/PII:0959437X9180032H?httpAccept=text/plain

9 November 2022

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Current Opinion in Genetics & Development

9 November 2022

published in

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15 August 2017

volume

1

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15 August 2017

issue

1

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15 August 2017

page(s)

4-10

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publication type of scholarly work

15 August 2017

review article

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Identification of the cystic fibrosis gene: chromosome walking and jumping

cites work

2

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

9 November 2022

3

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Identification of the cystic fibrosis gene: genetic analysis

9 November 2022

4

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Cystic fibrosis: a disease in electrolyte transport.

9 November 2022

5

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Abnormal regulation of ion channels in cystic fibrosis epithelia

9 November 2022

6

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Chloride and potassium channels in cystic fibrosis airway epithelia

9 November 2022

7

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Altered regulation of airway epithelial cell chloride channels in cystic fibrosis

9 November 2022

8

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase

9 November 2022

9

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Regulation of chloride channels by protein kinase C in normal and cystic fibrosis airway epithelia

9 November 2022

10

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Two types of chloride channel on duct cells cultured from human fetal pancreas

9 November 2022

11

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Low-conductance chloride channel activated by cAMP in the epithelial cell line T84

9 November 2022

13

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

9 November 2022

14

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Cystic Fibrosis Transmembrane Conductance Regulator: Nucleotide Binding to a Synthetic Peptide

9 November 2022

15

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

9 November 2022

A transport problem?

16

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

9 November 2022

18

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Benign missense variations in the cystic fibrosis gene

9 November 2022

19

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

9 November 2022

21

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

9 November 2022

22

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease

9 November 2022

23

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

A frame-shift mutation in the cystic fibrosis gene

9 November 2022

25

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Familial concordance of pancreatic function in cystic fibrosis

9 November 2022

26

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program

9 November 2022

27

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresis

9 November 2022

28

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

9 November 2022

29

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

9 November 2022

30

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

9 November 2022

31

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

9 November 2022

32

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

9 November 2022

33

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

9 November 2022

34

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

9 November 2022

35

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation

9 November 2022

36

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Increased sulfation of glycoconjugates by cultured nasal epithelial cells from patients with cystic fibrosis

9 November 2022

37

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

9 November 2022

39

1 reference

https://api.crossref.org/works/10.1016/0959-437X(91)80032-H

9 November 2022

Identifiers

1 reference

15 August 2017

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