Pages that link to "Q28513461"
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The following pages link to A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity (Q28513461):
Displaying 50 items.
- Bardet-Biedl syndrome 4 (human) (Q21418942) (← links)
- Bardet-Biedl syndrome 2 (human) (Q21418946) (← links)
- McKusick-Kaufman syndrome (Q21496604) (← links)
- A complex of BBS1 and NPHP7 is required for cilia motility in zebrafish (Q21558497) (← links)
- BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly (Q24295491) (← links)
- Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes (Q24298940) (← links)
- BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes (Q24301377) (← links)
- Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome (Q24313282) (← links)
- The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation (Q24316483) (← links)
- Motile cilia of human airway epithelia are chemosensory (Q24317210) (← links)
- BBS mutations modify phenotypic expression of CEP290-related ciliopathies (Q24317466) (← links)
- Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling (Q24317488) (← links)
- Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia (Q24317556) (← links)
- A BBSome subunit links ciliogenesis, microtubule stability, and acetylation (Q24336047) (← links)
- Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3 (Q24337720) (← links)
- The blind leading the obese: the molecular pathophysiology of a human obesity syndrome (Q24595694) (← links)
- Cellular Mechanisms of Ciliary Length Control (Q26769756) (← links)
- The role of primary cilia in the development and disease of the retina (Q26822720) (← links)
- Cilia in vertebrate development and disease (Q26829114) (← links)
- Update on the genetics of bardet-biedl syndrome (Q27026747) (← links)
- Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility. (Q27301367) (← links)
- Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling (Q27310130) (← links)
- Adult type 3 adenylyl cyclase-deficient mice are obese (Q27342322) (← links)
- Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform (Q27347938) (← links)
- Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
- The nonmotile ciliopathies (Q27967648) (← links)
- Ciliogenesis: building the cell's antenna (Q28000047) (← links)
- The BBSome controls IFT assembly and turnaround in cilia (Q28000109) (← links)
- CP110 and its network of partners coordinately regulate cilia assembly (Q28000138) (← links)
- Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant mice (Q28504740) (← links)
- Gene therapy prevents photoreceptor death and preserves retinal function in a Bardet-Biedl syndrome mouse model. (Q28507533) (← links)
- Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model (Q28511697) (← links)
- Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly (Q28512704) (← links)
- Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome (Q28577857) (← links)
- NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development (Q28586324) (← links)
- Pharmacological modulation of the retinal unfolded protein response in Bardet-Biedl syndrome reduces apoptosis and preserves light detection ability (Q28591411) (← links)
- Loss of Bardet-Biedl syndrome protein-8 (BBS8) perturbs olfactory function, protein localization, and axon targeting (Q28591892) (← links)
- Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse model (Q28594986) (← links)
- Contrasting vascular effects caused by loss of Bardet-Biedl syndrome genes (Q29347284) (← links)
- Bardet-Biedl syndrome 1 (human) (Q29530063) (← links)
- The primary cilium as a complex signaling center (Q29615254) (← links)
- Genomics of mature and immature olfactory sensory neurons (Q33623319) (← links)
- Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome (Q33934745) (← links)
- Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS) (Q33973018) (← links)
- Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning (Q33979104) (← links)
- Hippocampal and cortical primary cilia are required for aversive memory in mice (Q34128750) (← links)
- Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia (Q34158925) (← links)
- Ciliopathies: the trafficking connection (Q34207085) (← links)
- Identification and characterization of a novel allele of Caenorhabditis elegans bbs-7. (Q34653584) (← links)
- Functional analysis of BBS3 A89V that results in non-syndromic retinal degeneration (Q34718121) (← links)