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7. Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity. Dassie F; Favaretto F; Bettini S; Parolin M; Valenti M; Reschke F; Danne T; Vettor R; Milan G; Maffei P Endocrine; 2021 Mar; 71(3):618-625. PubMed ID: 33566311 [TBL] [Abstract][Full Text] [Related]
8. ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits. Hearn T J Mol Med (Berl); 2019 Jan; 97(1):1-17. PubMed ID: 30421101 [TBL] [Abstract][Full Text] [Related]
9. Diagnosis, treatment and genetic analysis of a case of Alstrom syndrome caused by compoud heterozygous mutation of Yang HJ; Li D; Bai HL; Zhang M; Huang J; Yuan XQ Yi Chuan; 2022 Dec; 44(12):1148-1157. PubMed ID: 36927560 [TBL] [Abstract][Full Text] [Related]
10. Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes. Nesmith JE; Hostelley TL; Leitch CC; Matern MS; Sethna S; McFarland R; Lodh S; Westlake CJ; Hertzano R; Ahmed ZM; Zaghloul NA Hum Mol Genet; 2019 Jul; 28(13):2212-2223. PubMed ID: 31220269 [TBL] [Abstract][Full Text] [Related]
11. Diabetes in the young - a case of Alström syndrome with myopathy. Bronson SC; Anand Moses CR; Periyandavar I; Dharmarajan P; Suresh E; Shanmugam A; Vasuki R; Venkatesh D; Amudha J J R Coll Physicians Edinb; 2015 Mar; 45(1):33-7. PubMed ID: 25874828 [TBL] [Abstract][Full Text] [Related]
12. A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient. Sanyoura M; Woudstra C; Halaby G; Baz P; Senée V; Guillausseau PJ; Zalloua P; Julier C Eur J Hum Genet; 2014 Jan; 22(1):140-3. PubMed ID: 23652376 [TBL] [Abstract][Full Text] [Related]
13. Female Alms1-deficient mice develop echocardiographic features of adult but not infantile Alström syndrome cardiomyopathy. McKay EJ; Luijten I; Broadway-Stringer S; Thomson A; Weng X; Gehmlich K; Gray GA; Semple RK Dis Model Mech; 2024 Jun; 17(6):. PubMed ID: 38756069 [TBL] [Abstract][Full Text] [Related]
14. Characterisation of infantile cardiomyopathy in Alström syndrome using ALMS1 knockout induced pluripotent stem cell derived cardiomyocyte model. Patel L; Roy A; Barlow J; O'Shea C; Nieves D; Azad AJ; Hall C; Davies B; Rath P; Pavlovic D; Chikermane A; Geberhiwot T; Steeds RP; Gehmlich K Mol Genet Metab; 2024; 143(1-2):108575. PubMed ID: 39243575 [TBL] [Abstract][Full Text] [Related]
15. The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey. Ozantürk A; Marshall JD; Collin GB; Düzenli S; Marshall RP; Candan Ş; Tos T; Esen İ; Taşkesen M; Çayır A; Öztürk Ş; Üstün İ; Ataman E; Karaca E; Özdemir TR; Erol İ; Eroğlu FK; Torun D; Parıltay E; Yılmaz-Güleç E; Karaca E; Atabek ME; Elçioğlu N; Satman İ; Möller C; Muller J; Naggert JK; Özgül RK J Hum Genet; 2015 Jan; 60(1):1-9. PubMed ID: 25296579 [TBL] [Abstract][Full Text] [Related]
16. Knockdown of the Alström syndrome-associated gene Alms1 in 3T3-L1 preadipocytes impairs adipogenesis but has no effect on cell-autonomous insulin action. Huang-Doran I; Semple RK Int J Obes (Lond); 2010 Oct; 34(10):1554-8. PubMed ID: 20514046 [TBL] [Abstract][Full Text] [Related]
17. Alström syndrome: insights into the pathogenesis of metabolic disorders. Girard D; Petrovsky N Nat Rev Endocrinol; 2011 Feb; 7(2):77-88. PubMed ID: 21135875 [TBL] [Abstract][Full Text] [Related]
18. GLUT4 defects in adipose tissue are early signs of metabolic alterations in Alms1GT/GT, a mouse model for obesity and insulin resistance. Favaretto F; Milan G; Collin GB; Marshall JD; Stasi F; Maffei P; Vettor R; Naggert JK PLoS One; 2014; 9(10):e109540. PubMed ID: 25299671 [TBL] [Abstract][Full Text] [Related]
19. Mesenchymal-specific Alms1 knockout in mice recapitulates metabolic features of Alström syndrome. McKay EJ; Luijten I; Weng X; Martinez de Morentin PB; De Frutos González E; Gao Z; Kolonin MG; Heisler LK; Semple RK Mol Metab; 2024 Jun; 84():101933. PubMed ID: 38583571 [TBL] [Abstract][Full Text] [Related]
20. Coronary artery disease in Alström syndrome. Jatti K; Paisey R; More R Eur J Hum Genet; 2012 Jan; 20(1):117-8. PubMed ID: 21897446 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]