MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis

Olivier Rosmorduc; Raoul Poupon; Brigitte Hermelin

doi:10.1053/gast.2001.23947

MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis

Gastroenterology ◽

10.1053/gast.2001.23947 ◽

2001 ◽

Vol 120 (6) ◽

pp. 1459-1467 ◽

Cited By ~ 208

Author(s):

Olivier Rosmorduc ◽

Raoul Poupon ◽

Brigitte Hermelin

Keyword(s):

Gene Defect ◽

Cholesterol Cholelithiasis

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Faculty Opinions recommendation of CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.3285962.3163054 ◽

2010 ◽

Author(s):

Francisco A Bonilla

Keyword(s):

Complex Formation ◽

Antibody Deficiency ◽

Gene Defect

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Faculty Opinions recommendation of CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.3285962.2971062 ◽

2010 ◽

Author(s):

Qiang Pan-Hammarström ◽

Giuseppe Cappellano

Keyword(s):

Complex Formation ◽

Antibody Deficiency ◽

Gene Defect

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Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: pathophysiology of biliary lipid secretion

The Journal of Lipid Research ◽

10.1016/s0022-2275(20)32430-5 ◽

1999 ◽

Vol 40 (11) ◽

pp. 2066-2079 ◽

Cited By ~ 12

Author(s):

David Q-H. Wang ◽

Frank Lammert ◽

Beverly Paigen ◽

Martin C. Carey

Keyword(s):

Inbred Mice ◽

Phenotypic Characterization ◽

Biliary Lipid ◽

Lipid Secretion ◽

Cholesterol Cholelithiasis

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Pigment vs cholesterol cholelithiasis

The American Journal of Digestive Diseases ◽

10.1007/bf01072459 ◽

1978 ◽

Vol 23 (10) ◽

pp. 877-882 ◽

Cited By ~ 18

Author(s):

Glenn L. Goodhart ◽

Matthew E. Levison ◽

Bruce W. Trotman ◽

Roger D. Soloway

Keyword(s):

Cholesterol Cholelithiasis

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Editorial: Is heterozygosity for a Wilson's disease gene defect an important underlying cause of infantile and childhood copper toxicosis syndromes?

The Journal of Trace Elements in Experimental Medicine ◽

10.1002/1520-670x(2000)13:3<249::aid-jtra1>3.0.co;2-l ◽

2000 ◽

Vol 13 (3) ◽

pp. 249-254 ◽

Cited By ~ 4

Author(s):

George J. Brewer

Keyword(s):

Wilson’S Disease ◽

Disease Gene ◽

Wilson's Disease ◽

Gene Defect ◽

Copper Toxicosis

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Phylogenetic approach in medical genetics. Evidence for deleterious role of ND5 gene defect in Leigh patients

Mitochondrion ◽

10.1016/j.mito.2006.08.048 ◽

2006 ◽

Vol 6 (5) ◽

pp. 19-20

Author(s):

S. Zhadanov ◽

E. Grechanina ◽

Yu. Grechanina ◽

V. Gusar ◽

N. Fedoseeva ◽

...

Keyword(s):

Medical Genetics ◽

Gene Defect ◽

Nd5 Gene

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Prevention of cholesterol cholelithiasis by dietary unsaturated fats in hormone-treated female hamsters

Lipids ◽

10.1007/bf02522888 ◽

1996 ◽

Vol 31 (7) ◽

pp. 721-727 ◽

Cited By ~ 3

Author(s):

Nariman Ayyad ◽

Bertram I. Cohen ◽

Akira Ohshima ◽

Erwin H. Mosbach

Keyword(s):

Cholesterol Cholelithiasis

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Gene defect corrected

Chemical & Engineering News ◽

10.1021/cen-v049n043.p009a ◽

1971 ◽

Vol 49 (43) ◽

pp. 9-10

Keyword(s):

Gene Defect

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Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect

Gut ◽

10.1136/gut.52.12.1752 ◽

2003 ◽

Vol 52 (12) ◽

pp. 1752-1755 ◽

Cited By ~ 93

Author(s):

W H de Vos tot Nederveen Cappel

Keyword(s):

Colorectal Cancer ◽

Surgical Treatment ◽

Decision Analysis ◽

Mismatch Repair ◽

Mismatch Repair Gene ◽

Gene Defect ◽

Repair Gene

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621. Persistent Long Term Lentiviral Correction of the CFTR Gene Defect in Cystic Fibrosis Mice

Molecular Therapy ◽

10.1016/s1525-0016(16)38062-5 ◽

2010 ◽

Vol 18 ◽

pp. S241-S242

Keyword(s):

Cystic Fibrosis ◽

Cftr Gene ◽

Gene Defect

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