Zeitlin PL - Search Results

1

Patients with mutations in Gsalpha have reduced activation of a downstream target in epithelial tissues due to haploinsufficiency.

Hsu SC, Groman JD, Merlo CA, Naughton K, Zeitlin PL, Germain-Lee EL, Boyle MP, Cutting GR. Hsu SC, et al. Among authors: zeitlin pl. J Clin Endocrinol Metab. 2007 Oct;92(10):3941-8. doi: 10.1210/jc.2007-0271. Epub 2007 Jul 24. J Clin Endocrinol Metab. 2007. PMID: 17652219

2

Respiratory epithelial gene expression in patients with mild and severe cystic fibrosis lung disease.

Wright JM, Merlo CA, Reynolds JB, Zeitlin PL, Garcia JG, Guggino WB, Boyle MP. Wright JM, et al. Among authors: zeitlin pl. Am J Respir Cell Mol Biol. 2006 Sep;35(3):327-36. doi: 10.1165/rcmb.2005-0359OC. Epub 2006 Apr 13. Am J Respir Cell Mol Biol. 2006. PMID: 16614352 Free PMC article.

3

A phase I trial of intranasal Moli1901 for cystic fibrosis.

Zeitlin PL, Boyle MP, Guggino WB, Molina L. Zeitlin PL, et al. Chest. 2004 Jan;125(1):143-9. doi: 10.1378/chest.125.1.143. Chest. 2004. PMID: 14718433 Clinical Trial.

4

Variants in mannose-binding lectin and tumour necrosis factor alpha affect survival in cystic fibrosis.

Buranawuti K, Boyle MP, Cheng S, Steiner LL, McDougal K, Fallin MD, Merlo C, Zeitlin PL, Rosenstein BJ, Mogayzel PJ Jr, Wang X, Cutting GR. Buranawuti K, et al. Among authors: zeitlin pl. J Med Genet. 2007 Mar;44(3):209-14. doi: 10.1136/jmg.2006.046318. Epub 2006 Dec 11. J Med Genet. 2007. PMID: 17158822 Free PMC article.

5

Evidence of CFTR function in cystic fibrosis after systemic administration of 4-phenylbutyrate.

Zeitlin PL, Diener-West M, Rubenstein RC, Boyle MP, Lee CK, Brass-Ernst L. Zeitlin PL, et al. Mol Ther. 2002 Jul;6(1):119-26. doi: 10.1006/mthe.2002.0639. Mol Ther. 2002. PMID: 12095312 Free article. Clinical Trial.

6

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: zeitlin pl. N Engl J Med. 2002 Aug 8;347(6):401-7. doi: 10.1056/NEJMoa011899. N Engl J Med. 2002. PMID: 12167682 Free article.

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: zeitlin pl. J Clin Invest. 1991 Dec;88(6):1880-5. doi: 10.1172/JCI115510. J Clin Invest. 1991. PMID: 1721624 Free PMC article.

8

A multicenter study of the effect of solution temperature on nasal potential difference measurements.

Boyle MP, Diener-West M, Milgram L, Knowles M, Foy C, Zeitlin P, Standaert T; Cystic Fibrosis Therapeutics Development Network Nasal PD Study Group. Boyle MP, et al. Chest. 2003 Aug;124(2):482-9. doi: 10.1378/chest.124.2.482. Chest. 2003. PMID: 12907532 Clinical Trial.

9

Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosis.

Dalesio NM, Aksit MA, Ahn K, Raraigh KS, Collaco JM, McGrath-Morrow S, Zeitlin PL, An SS, Cutting GR. Dalesio NM, et al. Among authors: zeitlin pl. Int Forum Allergy Rhinol. 2020 Jun;10(6):748-754. doi: 10.1002/alr.22548. Epub 2020 Apr 13. Int Forum Allergy Rhinol. 2020. PMID: 32282124 Free PMC article.

10

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: zeitlin pl. 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.

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