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Literature DB >> 10764694

The molecular and genetic base of congenital transport defects.

J F Desjeux¹.

Abstract

Entities: Disease

Mesh：

Year: 2000 PMID： 10764694 PMCID： PMC1727911 DOI： 10.1136/gut.46.5.585

Source DB: PubMed Journal: Gut ISSN： 0017-5749 Impact factor: 23.059

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22 in total

Review 1. Intestinal physiology and pathology in gene-targeted mouse models of cystic fibrosis.

Authors: B R Grubb; S E Gabriel
Journal: Am J Physiol Date: 1997-08

2. The human gene mutation database.

Authors: M Krawczak; D N Cooper
Journal: Trends Genet Date: 1997-03 Impact factor: 11.639

Review 3. Glucose transporters in the regulation of intestinal, renal, and liver glucose fluxes.

Authors: B Thorens
Journal: Am J Physiol Date: 1996-04

4. Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea.

Authors: P Höglund; S Haila; J Socha; L Tomaszewski; U Saarialho-Kere; M L Karjalainen-Lindsberg; K Airola; C Holmberg; A de la Chapelle; J Kere
Journal: Nat Genet Date: 1996-11 Impact factor: 38.330

5. Gene expression profile of aging and its retardation by caloric restriction.

Authors: C K Lee; R G Klopp; R Weindruch; T A Prolla
Journal: Science Date: 1999-08-27 Impact factor: 47.728

6. Molecular analysis of the fructose transporter gene (GLUT5) in isolated fructose malabsorption.

Authors: D Wasserman; J H Hoekstra; V Tolia; C J Taylor; B S Kirschner; J Takeda; G I Bell; R Taub; E B Rand
Journal: J Clin Invest Date: 1996-11-15 Impact factor: 14.808

7. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome.

Authors: J H Hansson; C Nelson-Williams; H Suzuki; L Schild; R Shimkets; Y Lu; C Canessa; T Iwasaki; B Rossier; R P Lifton
Journal: Nat Genet Date: 1995-09 Impact factor: 38.330

8. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Authors: D B Simon; C Nelson-Williams; M J Bia; D Ellison; F E Karet; A M Molina; I Vaara; F Iwata; H M Cushner; M Koolen; F J Gainza; H J Gitleman; R P Lifton
Journal: Nat Genet Date: 1996-01 Impact factor: 38.330

The molecular and genetic base of congenital transport defects.

Review 1. Intestinal physiology and pathology in gene-targeted mouse models of cystic fibrosis.

2. The human gene mutation database.

Review 3. Glucose transporters in the regulation of intestinal, renal, and liver glucose fluxes.

4. Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea.

5. Gene expression profile of aging and its retardation by caloric restriction.

6. Molecular analysis of the fructose transporter gene (GLUT5) in isolated fructose malabsorption.

7. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome.

8. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

9. Cystinuria: reduced lysine permeability at the brush border of intestinal membrane cells.

10. Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.

1. Prion proteins and the gut: une liaison dangereuse?

2. A 2-month-old with persistent diarrhea.

3. A computer model simulating human glucose absorption and metabolism in health and metabolic disease states.

4. Effect of genotype on duodenal expression of nutrient transporter genes in dairy cows.