Cutting GR - Search Results

1

Characterizing mucociliary clearance in young children with cystic fibrosis.

Laube BL, Carson KA, Evans CM, Aksit MA, Collaco JM, Richardson VL, Sharpless G, Zeitlin PL, Cutting GR, Mogayzel PJ. Laube BL, et al. Among authors: cutting gr. Pediatr Res. 2022 Feb;91(3):612-620. doi: 10.1038/s41390-021-01453-2. Epub 2021 Mar 22. Pediatr Res. 2022. PMID: 33753897 Free PMC article.

2

CFTR protein expression in primary and cultured epithelia.

Zeitlin PL, Crawford I, Lu L, Woel S, Cohen ME, Donowitz M, Montrose MH, Hamosh A, Cutting GR, Gruenert D, et al. Zeitlin PL, et al. Among authors: cutting gr. Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):344-7. doi: 10.1073/pnas.89.1.344. Proc Natl Acad Sci U S A. 1992. PMID: 1370353 Free PMC article.

3

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.

4

A cystic fibrosis bronchial epithelial cell line: immortalization by adeno-12-SV40 infection.

Zeitlin PL, Lu L, Rhim J, Cutting G, Stetten G, Kieffer KA, Craig R, Guggino WB. Zeitlin PL, et al. Am J Respir Cell Mol Biol. 1991 Apr;4(4):313-9. doi: 10.1165/ajrcmb/4.4.313. Am J Respir Cell Mol Biol. 1991. PMID: 1849726

5

Spectrum of mutations in cystic fibrosis.

Cutting GR. Cutting GR. J Bioenerg Biomembr. 1993 Feb;25(1):7-10. doi: 10.1007/BF00768062. J Bioenerg Biomembr. 1993. PMID: 7680032 Review.

6

Comparison of the clinical manifestations of cystic fibrosis in black and white patients.

Hamosh A, FitzSimmons SC, Macek M Jr, Knowles MR, Rosenstein BJ, Cutting GR. Hamosh A, et al. Among authors: cutting gr. J Pediatr. 1998 Feb;132(2):255-9. doi: 10.1016/s0022-3476(98)70441-x. J Pediatr. 1998. PMID: 9506637 Free article.

7

Analysis of ClC-2 channels as an alternative pathway for chloride conduction in cystic fibrosis airway cells.

Schwiebert EM, Cid-Soto LP, Stafford D, Carter M, Blaisdell CJ, Zeitlin PL, Guggino WB, Cutting GR. Schwiebert EM, et al. Among authors: cutting gr. Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3879-84. doi: 10.1073/pnas.95.7.3879. Proc Natl Acad Sci U S A. 1998. PMID: 9520461 Free PMC article.

8

Clinical implications of cystic fibrosis transmembrane conductance regulator mutations.

Mickle JE, Cutting GR. Mickle JE, et al. Among authors: cutting gr. Clin Chest Med. 1998 Sep;19(3):443-58, v. doi: 10.1016/s0272-5231(05)70092-7. Clin Chest Med. 1998. PMID: 9759548 Free article. Review.

9

Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population.

Wang X, Moylan B, Leopold DA, Kim J, Rubenstein RC, Togias A, Proud D, Zeitlin PL, Cutting GR. Wang X, et al. Among authors: cutting gr. JAMA. 2000 Oct 11;284(14):1814-9. doi: 10.1001/jama.284.14.1814. JAMA. 2000. PMID: 11025834

10

Variant cystic fibrosis phenotypes in the absence of CFTR mutations.

Groman JD, Meyer ME, Wilmott RW, Zeitlin PL, Cutting GR. Groman JD, et al. Among authors: cutting gr. N Engl J Med. 2002 Aug 8;347(6):401-7. doi: 10.1056/NEJMoa011899. N Engl J Med. 2002. PMID: 12167682 Free article.

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