Cutting GR - Search Results

1

Sources of Variation in Sweat Chloride Measurements in Cystic Fibrosis.

Collaco JM, Blackman SM, Raraigh KS, Corvol H, Rommens JM, Pace RG, Boelle PY, McGready J, Sosnay PR, Strug LJ, Knowles MR, Cutting GR. Collaco JM, et al. Among authors: cutting gr. Am J Respir Crit Care Med. 2016 Dec 1;194(11):1375-1382. doi: 10.1164/rccm.201603-0459OC. Am J Respir Crit Care Med. 2016. PMID: 27258095 Free PMC article.

2

Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians.

Cutting GR, Curristin SM, Nash E, Rosenstein BJ, Lerer I, Abeliovich D, Hill A, Graham C. Cutting GR, et al. Am J Hum Genet. 1992 Jun;50(6):1185-94. Am J Hum Genet. 1992. PMID: 1376017 Free PMC article.

3

Cystic fibrosis transmembrane conductance regulator and the etiology and pathogenesis of cystic fibrosis.

McIntosh I, Cutting GR. McIntosh I, et al. Among authors: cutting gr. FASEB J. 1992 Jul;6(10):2775-82. doi: 10.1096/fasebj.6.10.1378801. FASEB J. 1992. PMID: 1378801 Review.

4

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.

Chu CS, Trapnell BC, Curristin SM, Cutting GR, Crystal RG. Chu CS, et al. Among authors: cutting gr. J Clin Invest. 1992 Sep;90(3):785-90. doi: 10.1172/JCI115952. J Clin Invest. 1992. PMID: 1381723 Free PMC article.

5

Regulation of cystic fibrosis transmembrane conductance regulator (CFTR) gene transcription and alternative RNA splicing in a model of developing intestinal epithelium.

Montrose-Rafizadeh C, Blackmon DL, Hamosh A, Oliva MM, Hawkins AL, Curristin SM, Griffin CA, Yang VW, Guggino WB, Cutting GR, et al. Montrose-Rafizadeh C, et al. Among authors: cutting gr. J Biol Chem. 1992 Sep 25;267(27):19299-305. J Biol Chem. 1992. PMID: 1382071 Free article.

6

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

Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui LC, Antonarakis SE, Kazazian HH Jr. Cutting GR, et al. Nature. 1990 Jul 26;346(6282):366-9. doi: 10.1038/346366a0. Nature. 1990. PMID: 1695717

7

Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.

Hamosh A, Trapnell BC, Zeitlin PL, Montrose-Rafizadeh C, Rosenstein BJ, Crystal RG, Cutting GR. Hamosh A, et al. Among authors: cutting gr. J Clin Invest. 1991 Dec;88(6):1880-5. doi: 10.1172/JCI115510. J Clin Invest. 1991. PMID: 1721624 Free PMC article.

8

Both CFTR and outwardly rectifying chloride channels contribute to cAMP-stimulated whole cell chloride currents.

Schwiebert EM, Flotte T, Cutting GR, Guggino WB. Schwiebert EM, et al. Among authors: cutting gr. Am J Physiol. 1994 May;266(5 Pt 1):C1464-77. doi: 10.1152/ajpcell.1994.266.5.C1464. Am J Physiol. 1994. PMID: 7515570

9

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

Carroll TP, Morales MM, Fulmer SB, Allen SS, Flotte TR, Cutting GR, Guggino WB. Carroll TP, et al. Among authors: cutting gr. J Biol Chem. 1995 May 19;270(20):11941-6. doi: 10.1074/jbc.270.20.11941. J Biol Chem. 1995. PMID: 7538127 Free article.

10

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP.

Schwiebert EM, Egan ME, Hwang TH, Fulmer SB, Allen SS, Cutting GR, Guggino WB. Schwiebert EM, et al. Among authors: cutting gr. Cell. 1995 Jun 30;81(7):1063-73. doi: 10.1016/s0092-8674(05)80011-x. Cell. 1995. PMID: 7541313 Free article.

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