Pages that link to "Q28588862"
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The following pages link to Alms1-disrupted mice recapitulate human Alström syndrome (Q28588862):
Displaying 50 items.
- A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence (Q21092494) (← links)
- ALMS1, centrosome and basal body associated (Q21422688) (← links)
- Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731 (Q24299855) (← links)
- Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice (Q24304229) (← links)
- The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway (Q24338220) (← links)
- Specialized Cilia in Mammalian Sensory Systems (Q26785912) (← 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)
- Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
- The nonmotile ciliopathies (Q27967648) (← links)
- Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity (Q28567235) (← links)
- NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development (Q28586324) (← links)
- When cilia go bad: cilia defects and ciliopathies (Q29547198) (← links)
- Interactions of hearing loss and diabetes mellitus in the middle age CBA/CaJ mouse model of presbycusis. (Q30480730) (← links)
- Adaptations to climate in candidate genes for common metabolic disorders (Q33320199) (← links)
- The metabolic syndrome (Q33569142) (← 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)
- ALMS1-deficient fibroblasts over-express extra-cellular matrix components, display cell cycle delay and are resistant to apoptosis (Q33889416) (← links)
- Refining genotype-phenotype correlation in Alström syndrome through study of primary human fibroblasts (Q33906983) (← links)
- Systematic identification of personal tumor-specific neoantigens in chronic lymphocytic leukemia (Q33917224) (← links)
- Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1 (Q34032963) (← links)
- Primary cilia in pancreatic development and disease (Q34421859) (← links)
- The human obesity gene map: the 2005 update (Q34567973) (← links)
- The unique combination of dermatological and ocular phenotypes in Alström syndrome: severe presentation, early onset and two novel ALMS1 mutations (Q34708889) (← links)
- Population genomic analysis of ALMS1 in humans reveals a surprisingly complex evolutionary history (Q34961094) (← links)
- Molecular basis of the obesity associated with Bardet-Biedl syndrome (Q35087636) (← links)
- An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration (Q35221034) (← links)
- Novel Alu retrotransposon insertion leading to Alström syndrome (Q35691014) (← links)
- Alström Syndrome: Mutation Spectrum of ALMS1. (Q35762928) (← links)
- Decreased body weight and hepatic steatosis with altered fatty acid ethanolamide metabolism in aged L-Fabp -/- mice (Q35839688) (← links)
- Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis (Q35865471) (← links)
- The progression from obesity to type 2 diabetes in Alström syndrome. (Q35936590) (← links)
- Rare coding variants and X-linked loci associated with age at menarche (Q35961979) (← links)
- Histopathology of the human inner ear in Alström's syndrome (Q35967803) (← links)
- Molecular approach in the study of Alström syndrome: analysis of ten Spanish families. (Q36145920) (← links)
- Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins (Q36585455) (← links)
- Differences in the clinical spectrum of two adolescent male patients with Alström syndrome (Q36749428) (← links)
- The retinal ciliopathies. (Q36951820) (← links)
- Alström syndrome is associated with short stature and reduced GH reserve. (Q37033843) (← links)
- Mouse models in male fertility research (Q37084734) (← links)
- Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy (Q37111349) (← links)
- The Oak Ridge Polycystic Kidney mouse: modeling ciliopathies of mice and men (Q37118904) (← links)
- Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndrome. (Q37120432) (← links)
- Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments (Q37307190) (← links)
- Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndrome (Q37363953) (← links)
- Modeling ciliopathies: Primary cilia in development and disease (Q37383076) (← links)
- Cilia, Alström syndrome--molecular mechanisms and therapeutic perspectives (Q37682789) (← links)
- Utilization of conditional alleles to study the role of the primary cilium in obesity (Q37723492) (← links)
- Alström syndrome: insights into the pathogenesis of metabolic disorders (Q37816944) (← links)
- The impact of intronic single nucleotide polymorphisms and ethnic diversity for studies on the obesity gene FTO. (Q38038868) (← links)