Pages that link to "Q28507443"
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The following pages link to A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling (Q28507443):
Displaying 50 items.
- MKS transition zone complex subunit 1 (Q21436455) (← links)
- Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways (Q24302034) (← links)
- The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis (Q24303418) (← links)
- Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos (Q24304173) (← links)
- Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome (Q24622660) (← links)
- Identification of novel families and classification of the C2 domain superfamily elucidate the origin and evolution of membrane targeting activities in eukaryotes (Q24623162) (← links)
- The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization (Q26825968) (← links)
- Cilia in vertebrate development and disease (Q26829114) (← links)
- Lower urinary tract development and disease (Q27000375) (← links)
- Genetic, epigenetic, and environmental contributions to neural tube closure (Q27015138) (← links)
- Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeleton (Q27316402) (← links)
- Renal cystic disease proteins play critical roles in the organization of the olfactory epithelium (Q27342510) (← links)
- Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
- A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition (Q28000057) (← links)
- A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain (Q28000085) (← links)
- Disruption of a ciliary B9 protein complex causes Meckel syndrome (Q28114969) (← links)
- ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis (Q28507428) (← links)
- Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis (Q28509507) (← links)
- Forward genetics uncovers Transmembrane protein 107 as a novel factor required for ciliogenesis and Sonic hedgehog signaling (Q28510279) (← links)
- Complex interactions between genes controlling trafficking in primary cilia (Q28512423) (← links)
- Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies (Q28585520) (← links)
- Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndrome (Q28591420) (← links)
- Generation of mice with functional inactivation of talpid3, a gene first identified in chicken (Q28592864) (← links)
- Centrosomal protein CP110 controls maturation of the mother centriole during cilia biogenesis (Q28594586) (← links)
- The primary cilium: a signalling centre during vertebrate development (Q29547197) (← links)
- The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity. (Q30540974) (← links)
- The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data (Q31039716) (← links)
- The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate (Q33654636) (← links)
- Ciliopathies: the trafficking connection (Q34207085) (← links)
- B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis (Q35030818) (← links)
- The emerging face of primary cilia (Q35054504) (← links)
- TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone. (Q35394882) (← links)
- The transition zone protein Rpgrip1l regulates proteasomal activity at the primary cilium (Q35826045) (← links)
- The ciliary transition zone: from morphology and molecules to medicine (Q35902400) (← links)
- Using the avian mutant talpid2 as a disease model for understanding the oral-facial phenotypes of oral-facial-digital syndrome (Q35923482) (← links)
- SDCCAG8 Interacts with RAB Effector Proteins RABEP2 and ERC1 and Is Required for Hedgehog Signaling (Q36029226) (← links)
- Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins (Q36111257) (← links)
- The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling (Q36307485) (← links)
- Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins (Q36585455) (← links)
- The relationship between sonic Hedgehog signaling, cilia, and neural tube defects (Q36792187) (← links)
- Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms (Q36806446) (← links)
- Utilizing the chicken as an animal model for human craniofacial ciliopathies. (Q36829130) (← links)
- Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish (Q37079612) (← links)
- Drosophila sensory cilia lacking MKS proteins exhibit striking defects in development but only subtle defects in adults (Q37381267) (← links)
- Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms (Q37530115) (← links)
- The Ptch1(DL) mouse: a new model to study lambdoid craniosynostosis and basal cell nevus syndrome-associated skeletal defects (Q37571967) (← links)
- Open Sesame: How Transition Fibers and the Transition Zone Control Ciliary Composition. (Q37618918) (← links)
- The molecular regulation of vertebrate limb patterning (Q37778486) (← links)
- Molecular genetics and pathogenic mechanisms for the severe ciliopathies: insights into neurodevelopment and pathogenesis of neural tube defects (Q37812586) (← links)
- Development of the bile ducts: essentials for the clinical hepatologist (Q37975904) (← links)