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Impaired Ca2+ signaling due to steatosis mediates hepatic insulin resistance in Alstrom Syndrome mice that is reversed by GLP-1 analog treatment.

A Rare Case of Severe Dilated Cardiomyopathy in Early Infancy

Modeling NASH and NASH-Induced Hepatocellular Carcinoma: Faster and Better

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.

[Analysis of ALMS1 gene variants in seven patients with Alström syndrome].

Amiodarone-induced multiple organ damage in an Alström syndrome patient with end-stage renal disease and hepatic cirrhosis

The hedgehog signaling pathway is expressed in the adult mouse hypothalamus and modulated by fasting

Exocrine pancreas proteases regulate β-cell proliferation in zebrafish ciliopathy models and in murine systems

Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome.

The Hedgehog Signaling Pathway is Expressed in the Adult Mouse Hypothalamus and Modulated by Fasting

Alström syndrome with a novel mutation of ALMS1 and Graves’ hyperthyroidism: A case report and review of the literature

alms1 mutant zebrafish do not show hair cell phenotypes seen in other cilia mutants

The efficacy and safety of setmelanotide in individuals with Bardet-Biedl syndrome or Alström syndrome: Phase 3 trial design

Liver Fibrosis and Steatosis in Alström Syndrome: A Genetic Model for Metabolic Syndrome

Setmelanotide: First Approval

Neurocognitive assessment and DNA sequencing expand the phenotype and genotype spectrum of Alström syndrome

A Phase 3 Trial in Participants With Obesity Due to Bardet-Biedl Syndrome or Alström Syndrome: Efficacy and Safety of the Melanocortin 4 Receptor Agonist Setmelanotide

Anesthetic Considerations in Alström Syndrome: A Case Report

Translational readthrough of ciliopathy genes BBS2 and ALMS1 restores protein, ciliogenesis and function in patient fibroblasts

Prevalent ALMS1 Pathogenic Variants in Spanish Alström Patients

Adipose Tissue Malfunction Drives Metabolic Dysfunction in Alström Syndrome

Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity

ALMS1 Regulates TGF-β Signaling and Morphology of Primary Cilia

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

147-LB: PATAS, an Adipocyte-Targeted Peptide Approach to Treat Type 2 Diabetes and Associated Comorbidities

Alstrom syndrome: insulin resistance in young with congestive heart failure

Late diagnosis of Alstrom syndrome in a Yemenite-Jewish child

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