Why is "ALMS1" trending?

Search Interest Perspective

• Phosphoproteomic profiling highlights CDC42 and CDK2 as key players in the regulation of the TGF-β pathway in ALMS1 and BBS1 knockout models - Nature
• Depletion of ALMS1 affects TGF-β signalling pathway and downstream processes such as cell migration and adhesion capacity - Frontiers
• Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family - Wiley Online Library
• Alstrom Syndrome Research - News-Medical
• A New Therapeutic Target for Type 2 Diabetes Discovered Thanks to a Rare Disease - Salle de presse de l'Inserm
• A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient - Nature
• Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome - Frontiers
• Alström Syndrome: A Challenging Case Study of a Female Saudi Patient With Type 2 Diabetes Mellitus and Complete Vision Loss - Cureus
• Alström Diagnosis Pinpointed Early With Genetic Testing, Case Study Says - geneticobesitynews.com
• A child resides within a young adult: The first reported case of Alström syndrome in Bangladesh - Wiley Online Library
• Alström syndrome—wide clinical variability within the same variant: a case report and literature review - Frontiers
• Mutations in Alström protein impair terminal differentiation of cardiomyocytes - Nature
• Advanced Chronic Kidney Disease (CKD) in a Patient With Alstrom Syndrome - Cureus
• Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome - Nature
• Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome - Frontiers
• The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey - Nature
• Knockdown of the Alström syndrome-associated gene Alms1 in 3T3-L1 preadipocytes impairs adipogenesis but has no effect on cell-autonomous insulin action - Nature
• Mutation of ALMS1 , a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome - Nature
• Clinical utility gene card for: Alström syndrome - European Journal of Human Genetics - Nature
• Identification of ACBP as a potential target in ciliopathic obesity through multi-omics network analysis - Nature
• Adult-Onset Diabetes and Liver Fibrosis as Diagnostic Clues to Alström Syndrome: A Case Report - Cureus
• A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström Syndrome - Cureus
• Novel Peptide Could Create Pathway Against Insulin Resistance in Type 2 Diabetes - BioSpace
• Identification of novel genetic variants associated with feline cardiomyopathy using targeted next-generation sequencing - Nature
• New Drug Class in Development for Type 2 Diabetes - Technology Networks
• Towards a New Drug Class in the Treatment of Type 2 Diabetes - Monash University
• Innovative drug could improve type 2 diabetes treatment - Monash University