Pages that link to "Q28512332"
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The following pages link to Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis (Q28512332):
Displaying 50 items.
- A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence (Q21092494) (← links)
- Kinesin family member 3A (Q21495177) (← links)
- Dynein, axonemal, heavy chain 2 (Q21981058) (← links)
- Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome) (Q24290886) (← links)
- Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry (Q24292162) (← links)
- The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly (Q24293516) (← links)
- Role of the kinesin-2 family protein, KIF3, during mitosis (Q24296374) (← links)
- Protein phosphatase Dusp26 associates with KIF3 motor and promotes N-cadherin-mediated cell-cell adhesion (Q24319686) (← links)
- The two motor domains of KIF3A/B coordinate for processive motility and move at different speeds. (Q24537856) (← links)
- All kinesin superfamily protein, KIF, genes in mouse and human (Q24632779) (← links)
- Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia (Q24633410) (← links)
- Left-right determination: involvement of molecular motor KIF3, cilia, and nodal flow (Q24656688) (← links)
- CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders (Q24676633) (← links)
- Microscale imaging of cilia-driven fluid flow (Q26826635) (← links)
- A unified model for left-right asymmetry? Comparison and synthesis of molecular models of embryonic laterality (Q27008303) (← links)
- Tbx6 regulates left/right patterning in mouse embryos through effects on nodal cilia and perinodal signaling (Q27301024) (← links)
- Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome (Q27319191) (← links)
- High-resolution crystal structure and in vivo function of a kinesin-2 homologue in Giardia intestinalis (Q27650567) (← links)
- Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
- Protein particles in Chlamydomonas flagella undergo a transport cycle consisting of four phases (Q27919603) (← links)
- Intraflagellar transport (IFT) role in ciliary assembly, resorption and signalling. (Q27967638) (← links)
- Trafficking in and to the primary cilium (Q28000124) (← links)
- Disruption of a ciliary B9 protein complex causes Meckel syndrome (Q28114969) (← links)
- Kif3a interacts with Dynactin subunit p150 Glued to organize centriole subdistal appendages (Q28117905) (← links)
- A human laterality disorder caused by a homozygous deleterious mutation in MMP21 (Q28118429) (← links)
- A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function (Q28118538) (← links)
- Intraflagellar transport (Q28131775) (← links)
- IFT20 links kinesin II with a mammalian intraflagellar transport complex that is conserved in motile flagella and sensory cilia (Q28181491) (← links)
- Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta (Q28199148) (← links)
- Biochemical and molecular characterization of diseases linked to motor proteins (Q28209818) (← links)
- Establishment of vertebrate left-right asymmetry (Q28218181) (← links)
- The flagellum of trypanosomes (Q28271824) (← links)
- Cilia and developmental signaling (Q28302606) (← links)
- Kif3a deficiency reverses the skeletal abnormalities in Pkd1 deficient mice by restoring the balance between osteogenesis and adipogenesis (Q28476413) (← links)
- The KIF3 motor transports N-cadherin and organizes the developing neuroepithelium (Q28504719) (← links)
- Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice (Q28505979) (← links)
- Hippi is essential for node cilia assembly and Sonic hedgehog signaling (Q28506946) (← links)
- Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries (Q28507104) (← links)
- Intact lysosome transport and phagosome function despite kinectin deficiency (Q28507426) (← links)
- The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiation (Q28507794) (← links)
- Monocilia in the embryonic mouse heart suggest a direct role for cilia in cardiac morphogenesis (Q28508699) (← links)
- Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice (Q28511679) (← links)
- Regulation of microtubule dynamics and myogenic differentiation by MURF, a striated muscle RING-finger protein (Q28513866) (← links)
- Targeting of beta-arrestin2 to the centrosome and primary cilium: role in cell proliferation control (Q28571736) (← links)
- The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development (Q28584722) (← links)
- Molecular motor KIF1C is not essential for mouse survival and motor-dependent retrograde Golgi apparatus-to-endoplasmic reticulum transport (Q28585112) (← links)
- Association of the testis-specific TRIM/RBCC protein RNF33/TRIM60 with the cytoplasmic motor proteins KIF3A and KIF3B (Q28585568) (← links)
- Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4 (Q28586893) (← links)
- Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking (Q28588535) (← links)
- Cluap1 localizes preferentially to the base and tip of cilia and is required for ciliogenesis in the mouse embryo (Q28588539) (← links)