(Q35150488)

6 August 2017

1 reference

title

The spectrum of cystic fibrosis mutations (English)

1 reference

6 August 2017

0 references

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

20 November 2023

author name string

L. C. Tsui

1

1 reference

PubMed ID

1279852

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1279852

8 September 2022

language of work or name

1 reference

1 November 1992

1 reference

PubMed ID

1279852

full work available at URL

6 August 2017

https://api.elsevier.com/content/article/PII:016895259290301J?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

https://api.elsevier.com/content/article/PII:016895259290301J?httpAccept=text/plain

20 November 2023

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

20 November 2023

1 reference

6 August 2017

8

1 reference

6 August 2017

392-398

1 reference

6 August 2017

11

1 reference

Identification of the cystic fibrosis gene: chromosome walking and jumping

6 August 2017

3

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

4

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Identification of the cystic fibrosis gene: genetic analysis

20 November 2023

5

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

20 November 2023

6

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

20 November 2023

7

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Cystic fibrosis: molecular biology and therapeutic implications

20 November 2023

8

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

9

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

10

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics

20 November 2023

14

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephew

20 November 2023

16

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Nucleoside triphosphates are required to open the CFTR chloride channel.

20 November 2023

19

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

20

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences.

20 November 2023

21

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

20 November 2023

22

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

20 November 2023

23

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

24

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

20 November 2023

25

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

20 November 2023

26

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

20 November 2023

27

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Familial concordance of pancreatic function in cystic fibrosis

20 November 2023

28

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

30

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

31

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens

20 November 2023

32

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis

20 November 2023

33

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels

20 November 2023

34

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

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

20 November 2023

35

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

20 November 2023

37

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosis

20 November 2023

38

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A----G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene

20 November 2023

39

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation

20 November 2023

40

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

An animal model for cystic fibrosis made by gene targeting

20 November 2023

41

1 reference

https://api.crossref.org/works/10.1016/0168-9525(92)90301-J

20 November 2023

Identifiers

1 reference

6 August 2017

1 reference

PubMed ID

1279852