Welsh MJ[au] - Search Results

Year	Number of Results
1963	1
1965	1
1975	1
1976	1
1977	2
1978	4
1979	1
1980	7
1981	3
1982	4
1983	11
1984	4
1985	6
1986	14
1987	6
1988	8
1989	9
1990	20
1991	17
1992	21
1993	22
1994	19
1995	25
1996	19
1997	16
1998	21
1999	23
2000	18
2001	19
2002	11
2003	15
2004	18
2005	12
2006	7
2007	9
2008	12
2009	11
2010	9
2011	9
2012	13
2013	8
2014	14
2015	8
2016	12
2017	5
2018	6
2019	4
2020	6
2021	4

1

Origins of cystic fibrosis lung disease.

Stoltz DA, Meyerholz DK, Welsh MJ. Stoltz DA, et al. Among authors: welsh mj. N Engl J Med. 2015 Jan 22;372(4):351-62. doi: 10.1056/NEJMra1300109. N Engl J Med. 2015. PMID: 25607428 Free PMC article. Review. No abstract available.

2

Enhancing glycolysis attenuates Parkinson's disease progression in models and clinical databases.

Cai R, Zhang Y, Simmering JE, Schultz JL, Li Y, Fernandez-Carasa I, Consiglio A, Raya A, Polgreen PM, Narayanan NS, Yuan Y, Chen Z, Su W, Han Y, Zhao C, Gao L, Ji X, Welsh MJ, Liu L. Cai R, et al. Among authors: welsh mj. J Clin Invest. 2019 Oct 1;129(10):4539-4549. doi: 10.1172/JCI129987. J Clin Invest. 2019. PMID: 31524631 Free PMC article.

3

Cystic fibrosis carriers are at increased risk for a wide range of cystic fibrosis-related conditions.

Miller AC, Comellas AP, Hornick DB, Stoltz DA, Cavanaugh JE, Gerke AK, Welsh MJ, Zabner J, Polgreen PM. Miller AC, et al. Among authors: welsh mj. Proc Natl Acad Sci U S A. 2020 Jan 21;117(3):1621-1627. doi: 10.1073/pnas.1914912117. Epub 2019 Dec 27. Proc Natl Acad Sci U S A. 2020. PMID: 31882447 Free PMC article.

4

Structure and function of the CFTR chloride channel.

Sheppard DN, Welsh MJ. Sheppard DN, et al. Among authors: welsh mj. Physiol Rev. 1999 Jan;79(1 Suppl):S23-45. doi: 10.1152/physrev.1999.79.1.S23. Physiol Rev. 1999. PMID: 9922375 Free article. Review.

5

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis.

Welsh MJ, Smith AE. Welsh MJ, et al. Cell. 1993 Jul 2;73(7):1251-4. doi: 10.1016/0092-8674(93)90353-r. Cell. 1993. PMID: 7686820 Review. No abstract available.

6

Small-molecule ion channels increase host defences in cystic fibrosis airway epithelia.

Muraglia KA, Chorghade RS, Kim BR, Tang XX, Shah VS, Grillo AS, Daniels PN, Cioffi AG, Karp PH, Zhu L, Welsh MJ, Burke MD. Muraglia KA, et al. Among authors: welsh mj. Nature. 2019 Mar;567(7748):405-408. doi: 10.1038/s41586-019-1018-5. Epub 2019 Mar 13. Nature. 2019. PMID: 30867598 Free PMC article.

7

Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis Mucus.

Xie Y, Lu L, Tang XX, Moninger TO, Huang TJ, Stoltz DA, Welsh MJ. Xie Y, et al. Among authors: welsh mj. Dev Cell. 2020 Aug 24;54(4):488-500.e5. doi: 10.1016/j.devcel.2020.07.002. Epub 2020 Jul 29. Dev Cell. 2020. PMID: 32730755

8

Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung.

Pezzulo AA, Tang XX, Hoegger MJ, Abou Alaiwa MH, Ramachandran S, Moninger TO, Karp PH, Wohlford-Lenane CL, Haagsman HP, van Eijk M, Bánfi B, Horswill AR, Stoltz DA, McCray PB Jr, Welsh MJ, Zabner J. Pezzulo AA, et al. Among authors: welsh mj. Nature. 2012 Jul 4;487(7405):109-13. doi: 10.1038/nature11130. Nature. 2012. PMID: 22763554 Free PMC article.

9

Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections.

Hisert KB, Heltshe SL, Pope C, Jorth P, Wu X, Edwards RM, Radey M, Accurso FJ, Wolter DJ, Cooke G, Adam RJ, Carter S, Grogan B, Launspach JL, Donnelly SC, Gallagher CG, Bruce JE, Stoltz DA, Welsh MJ, Hoffman LR, McKone EF, Singh PK. Hisert KB, et al. Among authors: welsh mj. Am J Respir Crit Care Med. 2017 Jun 15;195(12):1617-1628. doi: 10.1164/rccm.201609-1954OC. Am J Respir Crit Care Med. 2017. PMID: 28222269 Free PMC article.

10

An in vitro model of differentiated human airway epithelia. Methods for establishing primary cultures.

Karp PH, Moninger TO, Weber SP, Nesselhauf TS, Launspach JL, Zabner J, Welsh MJ. Karp PH, et al. Among authors: welsh mj. Methods Mol Biol. 2002;188:115-37. doi: 10.1385/1-59259-185-X:115. Methods Mol Biol. 2002. PMID: 11987537 No abstract available.

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