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Items: 10

1.

A simple, fast and inexpensive method for mutation scanning of CFTR gene.

Figueredo Lago JE, Armas Cayarga A, González González YJ, Collazo Mesa T.

BMC Med Genet. 2017 May 25;18(1):58. doi: 10.1186/s12881-017-0420-9.

2.

Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator.

Bartoszewski R, Króliczewski J, Piotrowski A, Jasiecka AJ, Bartoszewska S, Vecchio-Pagan B, Fu L, Sobolewska A, Matalon S, Cutting GR, Rowe SM, Collawn JF.

Cell Mol Biol Lett. 2016 Oct 19;21:23. doi: 10.1186/s11658-016-0025-x. eCollection 2016. Review.

3.

CFTR-mediated anion secretion across intestinal epithelium-like Caco-2 monolayer under PTH stimulation is dependent on intermediate conductance K+ channels.

Jantarajit W, Lertsuwan K, Teerapornpuntakit J, Krishnamra N, Charoenphandhu N.

Am J Physiol Cell Physiol. 2017 Jul 1;313(1):C118-C129. doi: 10.1152/ajpcell.00010.2017. Epub 2017 May 10.

PMID:
28490422
4.

ABC gene expression profiles have clinical importance and possibly form a new hallmark of cancer.

Dvorak P, Pesta M, Soucek P.

Tumour Biol. 2017 May;39(5):1010428317699800. doi: 10.1177/1010428317699800.

PMID:
28468577
5.

Pancreatitis Overview.

LaRusch J, Solomon S, Whitcomb DC.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2014 Mar 13.

6.

Cystic Fibrosis and Congenital Absence of the Vas Deferens.

Ong T, Marshall SG, Karczeski BA, Sternen DL, Cheng E, Cutting GR.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2001 Mar 26 [updated 2017 Feb 2].

7.

A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene.

Lissens W, Bonduelle M, Malfroot A, Dab I, Liebaers I.

Hum Mol Genet. 1992 Sep;1(6):441-2. No abstract available.

PMID:
1284530
8.

Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP.

Shackleton S, Beards F, Harris A.

Hum Mol Genet. 1992 Sep;1(6):439-40. No abstract available.

PMID:
1284529
9.

A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene.

Cheadle JP, Meredith AL, al-Jader LN.

Hum Mol Genet. 1992 May;1(2):123-5. No abstract available.

PMID:
1284468
10.

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

Jones CT, McIntosh I, Keston M, Ferguson A, Brock DJ.

Hum Mol Genet. 1992 Apr;1(1):11-7.

PMID:
1284466

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