These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 37951511)

  • 1. Impaired digestive function of sucrase-isomaltase in a complex with the Greenlandic sucrase-isomaltase variant.
    Tannous S; Naim HY
    Biochim Biophys Acta Mol Basis Dis; 2024 Feb; 1870(2):166947. PubMed ID: 37951511
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital sucrase-isomaltase deficiency in Türkiye; a single center experience.
    Barut D; Kıran Taşcı E; Kunay B; Güven B; Aksoy B; Çağan Appak Y; Karakoyun M; Çetin F; Selimoğlu A; Onay H; Aydoğdu S
    Scand J Gastroenterol; 2024 Jun; 59(6):647-651. PubMed ID: 38459691
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe pathogenic variants of intestinal sucrase-isomaltase interact avidly with the wild type enzyme and negatively impact its function and trafficking.
    Husein DM; Rizk S; Hoter A; Wanes D; D'Amato M; Naim HY
    Biochim Biophys Acta Mol Basis Dis; 2022 Nov; 1868(11):166523. PubMed ID: 35985447
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency.
    Husein DM; Wanes D; Marten LM; Zimmer KP; Naim HY
    Nutrients; 2019 Sep; 11(10):. PubMed ID: 31557950
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The glucose-regulated protein GRP94 interacts avidly in the endoplasmic reticulum with sucrase-isomaltase isoforms that are associated with congenital sucrase-isomaltase deficiency.
    Hoter A; Naim HY
    Int J Biol Macromol; 2021 Sep; 186():237-243. PubMed ID: 34242650
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
    Husein DM; Rizk S; Naim HY
    Nutrients; 2020 Dec; 13(1):. PubMed ID: 33375084
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
    Gericke B; Amiri M; Scott CR; Naim HY
    Biochim Biophys Acta Mol Basis Dis; 2017 Mar; 1863(3):817-826. PubMed ID: 28062276
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Naturally occurring mutations in intestinal sucrase-isomaltase provide evidence for the existence of an intracellular sorting signal in the isomaltase subunit.
    Fransen JA; Hauri HP; Ginsel LA; Naim HY
    J Cell Biol; 1991 Oct; 115(1):45-57. PubMed ID: 1717481
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
    Jacob R; Zimmer KP; Schmitz J; Naim HY
    J Clin Invest; 2000 Jul; 106(2):281-7. PubMed ID: 10903344
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.
    Marcadier JL; Boland M; Scott CR; Issa K; Wu Z; McIntyre AD; Hegele RA; Geraghty MT; Lines MA
    CMAJ; 2015 Feb; 187(2):102-107. PubMed ID: 25452324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of Sucrase-Isomaltase Function Increases Acetate Levels and Improves Metabolic Health in Greenlandic Cohorts.
    Andersen MK; Skotte L; Jørsboe E; Polito R; Stæger FF; Aldiss P; Hanghøj K; Waples RK; Santander CG; Grarup N; Dahl-Petersen IK; Diaz LJ; Overvad M; Senftleber NK; Søborg B; Larsen CVL; Lemoine C; Pedersen O; Feenstra B; Bjerregaard P; Melbye M; Jørgensen ME; Færgeman NJ; Koch A; Moritz T; Gillum MP; Moltke I; Hansen T; Albrechtsen A
    Gastroenterology; 2022 Apr; 162(4):1171-1182.e3. PubMed ID: 34914943
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic Loss of Sucrase-Isomaltase Function: Mechanisms, Implications, and Future Perspectives.
    Senftleber NK; Ramne S; Moltke I; Jørgensen ME; Albrechtsen A; Hansen T; Andersen MK
    Appl Clin Genet; 2023; 16():31-39. PubMed ID: 36994449
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency.
    Smith H; Romero B; Flood E; Boney A
    Qual Life Res; 2021 Aug; 30(8):2329-2338. PubMed ID: 33772704
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.
    Ritz V; Alfalah M; Zimmer KP; Schmitz J; Jacob R; Naim HY
    Gastroenterology; 2003 Dec; 125(6):1678-85. PubMed ID: 14724820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.
    Sander P; Alfalah M; Keiser M; Korponay-Szabo I; Kovács JB; Leeb T; Naim HY
    Hum Mutat; 2006 Jan; 27(1):119. PubMed ID: 16329100
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Healthcare Burden in Greenland of Gastrointestinal Symptoms in Adults with Inherited Loss of Sucrase-Isomaltase Function.
    Andersen K; Hansen T; Jørgensen ME; Senftleber N
    Appl Clin Genet; 2024; 17():15-21. PubMed ID: 38328770
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.
    Keiser M; Alfalah M; Pröpsting MJ; Castelletti D; Naim HY
    J Biol Chem; 2006 May; 281(20):14393-9. PubMed ID: 16543230
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cloning of sucrase-isomaltase cDNA in the house musk shrew Suncus murinus and identification of a mutation responsible for isolated sucrase deficiency.
    Ito T; Hayashi Y; Ohmori S; Oda S; Seo H
    J Biol Chem; 1998 Jun; 273(26):16464-9. PubMed ID: 9632713
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 13C-Labeled-Starch Breath Test in Congenital Sucrase-isomaltase Deficiency.
    Robayo-Torres CC; Diaz-Sotomayor M; Hamaker BR; Baker SS; Chumpitazi BP; Opekun AR; Nichols BL
    J Pediatr Gastroenterol Nutr; 2018 Jun; 66 Suppl 3(Suppl 3):S61-S64. PubMed ID: 29762381
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetics of sucrose metabolism disorders in different population groups].
    Kozlov AI; Malyarchuk BA
    Vopr Pitan; 2024; 93(2):52-62. PubMed ID: 38809799
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.