Chen JM - Search Results

1

No Association Between CEL-HYB Hybrid Allele and Chronic Pancreatitis in Asian Populations.

Zou WB, Boulling A, Masamune A, Issarapu P, Masson E, Wu H, Sun XT, Hu LH, Zhou DZ, He L, Fichou Y, Nakano E, Hamada S, Kakuta Y, Kume K, Isayama H, Paliwal S, Mani KR, Bhaskar S, Cooper DN, Férec C, Shimosegawa T, Chandak GR, Chen JM, Li ZS, Liao Z. Zou WB, et al. Among authors: chen jm. Gastroenterology. 2016 Jun;150(7):1558-1560.e5. doi: 10.1053/j.gastro.2016.02.071. Epub 2016 Mar 3. Gastroenterology. 2016. PMID: 26946345 Free PMC article.

2

Exclusion of anionic trypsinogen and mesotrypsinogen involvement in hereditary pancreatitis without cationic trypsinogen gene mutations.

Chen JM, Audrezet MP, Mercier B, Quere I, Ferec C. Chen JM, et al. Scand J Gastroenterol. 1999 Aug;34(8):831-2. doi: 10.1080/003655299750025796. Scand J Gastroenterol. 1999. PMID: 10499487 No abstract available.

3

The A16V signal peptide cleavage site mutation in the cationic trypsinogen gene and chronic pancreatitis.

Chen JM, Raguenes O, Ferec C, Deprez PH, Verellen-Dumoulin C, Andriulli A. Chen JM, et al. Gastroenterology. 1999 Dec;117(6):1508-9. doi: 10.1016/s0016-5085(99)70313-6. Gastroenterology. 1999. PMID: 10610343 No abstract available.

4

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.

5

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

6

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.

7

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.

8

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

9

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.

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,953 results

Search Page