Chen JM - Search Results

1

A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis.

Fjeld K, Weiss FU, Lasher D, Rosendahl J, Chen JM, Johansson BB, Kirsten H, Ruffert C, Masson E, Steine SJ, Bugert P, Cnop M, Grützmann R, Mayerle J, Mössner J, Ringdal M, Schulz HU, Sendler M, Simon P, Sztromwasser P, Torsvik J, Scholz M, Tjora E, Férec C, Witt H, Lerch MM, Njølstad PR, Johansson S, Molven A. Fjeld K, et al. Among authors: chen jm. Nat Genet. 2015 May;47(5):518-522. doi: 10.1038/ng.3249. Epub 2015 Mar 16. Nat Genet. 2015. PMID: 25774637 Free PMC article.

2

Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis.

Chen JM, Mercier B, Ferec C. Chen JM, et al. Gut. 1999 Dec;45(6):916. doi: 10.1136/gut.45.6.916. Gut. 1999. PMID: 10644199 Free PMC article. No abstract available.

3

Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis.

Chen JM, Mercier B, Audrezet MP, Ferec C. Chen JM, et al. J Med Genet. 2000 Jan;37(1):67-9. doi: 10.1136/jmg.37.1.67. J Med Genet. 2000. PMID: 10691414 Free PMC article. No abstract available.

4

Genes, cloned cDNAs, and proteins of human trypsinogens and pancreatitis-associated cationic trypsinogen mutations.

Chen JM, Ferec C. Chen JM, et al. Pancreas. 2000 Jul;21(1):57-62. doi: 10.1097/00006676-200007000-00052. Pancreas. 2000. PMID: 10881933

5

Molecular basis of hereditary pancreatitis.

Chen JM, Ferec C. Chen JM, et al. Eur J Hum Genet. 2000 Jul;8(7):473-9. doi: 10.1038/sj.ejhg.5200492. Eur J Hum Genet. 2000. PMID: 10909845 Review.

6

Wanted: a consensus nomenclature for cationic trypsinogen mutations.

Chen JM, Ferec C. Chen JM, et al. Gastroenterology. 2000 Jul;119(1):277. doi: 10.1016/s0016-5085(00)70073-4. Gastroenterology. 2000. PMID: 10928834 No abstract available.

7

Origin and implication of the hereditary pancreatitis-associated N21I mutation in the cationic trypsinogen gene.

Chen JM, Ferec C. Chen JM, et al. Hum Genet. 2000 Jan;106(1):125-6. doi: 10.1007/s004390051019. Hum Genet. 2000. PMID: 10982192

8

Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulator.

Chen JM, Scotet V, Ferec C. Chen JM, et al. Mol Genet Metab. 2000 Sep-Oct;71(1-2):245-9. doi: 10.1006/mgme.2000.3041. Mol Genet Metab. 2000. PMID: 11001817 Review.

9

A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis.

Chen JM, Raguenes O, Ferec C, Deprez PH, Verellen-Dumoulin C. Chen JM, et al. J Med Genet. 2000 Nov;37(11):E36. doi: 10.1136/jmg.37.11.e36. J Med Genet. 2000. PMID: 11073545 Free PMC article. No abstract available.

10

Gene conversion-like missense mutations in the human cationic trypsinogen gene and insights into the molecular evolution of the human trypsinogen family.

Chen JM, Ferec C. Chen JM, et al. Mol Genet Metab. 2000 Nov;71(3):463-9. doi: 10.1006/mgme.2000.3086. Mol Genet Metab. 2000. PMID: 11073713 Review.

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