Pages that link to "Q24338220"
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The following pages link to The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway (Q24338220):
Displaying 41 items.
- ALMS1 centrosome and basal body associated protein (Q21109398) (← links)
- ALMS1, centrosome and basal body associated (Q21422688) (← links)
- Actinin alpha 3 (Q21491079) (← links)
- Actinin alpha 4 (Q21491080) (← links)
- Actinin, alpha 1 (Q21492714) (← links)
- Actinin alpha 2 (Q21493830) (← links)
- Alström syndrome: current perspectives (Q26801117) (← links)
- The role of primary cilia in the development and disease of the retina (Q26822720) (← links)
- GLUT4 defects in adipose tissue are early signs of metabolic alterations in Alms1GT/GT, a mouse model for obesity and insulin resistance (Q27339452) (← links)
- Basal body proteins regulate Notch signaling through endosomal trafficking (Q33687596) (← links)
- The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey (Q33768990) (← links)
- Refining genotype-phenotype correlation in Alström syndrome through study of primary human fibroblasts (Q33906983) (← links)
- Alström Syndrome: Mutation Spectrum of ALMS1. (Q35762928) (← links)
- Characteristics of cardiomyopathy in Alström syndrome: Prospective single-center data on 38 patients (Q36404674) (← links)
- Primary cilia in energy balance signaling and metabolic disorder (Q36685669) (← links)
- Glioma invasion mediated by the p75 neurotrophin receptor (p75(NTR)/CD271) requires regulated interaction with PDLIM1. (Q36707721) (← links)
- Cilia and coordination of signaling networks during heart development (Q38171918) (← links)
- The non-muscle functions of actinins: an update. (Q38195854) (← links)
- A Review of Secondary Photoreceptor Degenerations in Systemic Disease (Q38283115) (← links)
- Metabolic regulation and energy homeostasis through the primary Cilium (Q38301656) (← links)
- Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alström syndrome (Q38671656) (← links)
- An Actin Network Dispatches Ciliary GPCRs into Extracellular Vesicles to Modulate Signaling. (Q38724382) (← links)
- Ciliopathies: Genetics in Pediatric Medicine (Q38759596) (← links)
- Mutations in Alström protein impair terminal differentiation of cardiomyocytes (Q38840384) (← links)
- The BLOC-1 Subunit Pallidin Facilitates Activity-Dependent Synaptic Vesicle Recycling. (Q38895201) (← links)
- Respiratory manifestations in 38 patients with Alström syndrome (Q38913095) (← links)
- Long-term clinical follow-up and molecular testing for diagnosis of the first Tunisian family with Alström syndrome (Q38937337) (← links)
- Topical carbonic anhydrase inhibitors in macular edema associated with Alström syndrome (Q47959986) (← links)
- Ophthalmic features of cone-rod dystrophy caused by pathogenic variants in the ALMS1 gene (Q48200102) (← links)
- Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea (Q50528573) (← links)
- Oncoprotein CIP2A promotes the disassembly of primary cilia and inhibits glycolytic metabolism. (Q52680870) (← links)
- Comprehensive Endocrine-Metabolic Evaluation of Patients with Alström Syndrome Compared to BMI-Matched Controls. (Q53689125) (← links)
- ATOH1/RFX1/RFX3 transcription factors facilitate the differentiation and characterisation of inner ear hair cell-like cells from patient-specific induced pluripotent stem cells harbouring A8344G mutation of mitochondrial DNA. (Q55054804) (← links)
- Role of Alström syndrome 1 in the regulation of blood pressure and renal function (Q58617307) (← links)
- 661W Photoreceptor Cell Line as a Cell Model for Studying Retinal Ciliopathies (Q63488037) (← links)
- Auditory and otologic profile of Alström syndrome: Comprehensive single center data on 38 patients (Q88220463) (← links)
- Genes associated with inflammation and the cell cycle may serve as biomarkers for the diagnosis and prognosis of acute myocardial infarction in a Chinese population (Q88912552) (← links)
- Alström syndrome: Renal findings in correlation with obesity, insulin resistance, dyslipidemia and cardiomyopathy in 38 patients prospectively evaluated at the NIH clinical center (Q90670599) (← links)
- A case report of two siblings with Alstrom syndrome without hearing loss associated with two new ALMS1 variants (Q91763211) (← links)
- ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits (Q93021066) (← links)
- A very early diagnosis of Alstrӧm syndrome by next generation sequencing (Q99635683) (← links)