Pages that link to "Q35491643"
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The following pages link to Structural analysis of muscle development: transverse tubules, sarcoplasmic reticulum, and the triad (Q35491643):
Displaying 50 items.
- Characterization of human junctophilin subtype genes (Q22254593) (← links)
- New molecular components supporting ryanodine receptor-mediated Ca(2+) release: roles of junctophilin and TRIC channel in embryonic cardiomyocytes (Q24309139) (← links)
- Obscurin is a ligand for small ankyrin 1 in skeletal muscle (Q24554297) (← links)
- Regulation of Bin1 SH3 domain binding by phosphoinositides (Q24561373) (← links)
- 3D Structure of the Dihydropyridine Receptor of Skeletal Muscle (Q26766447) (← links)
- Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy (Q28300361) (← links)
- Abnormal junctional membrane structures in cardiac myocytes expressing ectopic junctophilin type 1 (Q28507665) (← links)
- Caveolin-3 associates with developing T-tubules during muscle differentiation (Q28511690) (← links)
- Junctophilin-mediated channel crosstalk essential for cerebellar synaptic plasticity. (Q28511849) (← links)
- Vesicle budding from endoplasmic reticulum is involved in calsequestrin routing to sarcoplasmic reticulum of skeletal muscles (Q28513853) (← links)
- Embryonic lethality and abnormal cardiac myocytes in mice lacking ryanodine receptor type 2. (Q28584945) (← links)
- Caveolin-1(-/-)- and caveolin-2(-/-)-deficient mice both display numerous skeletal muscle abnormalities, with tubular aggregate formation (Q28590340) (← links)
- Functional uncoupling between Ca2+ release and afterhyperpolarization in mutant hippocampal neurons lacking junctophilins (Q28591751) (← links)
- Junctophilins (Q29391444) (← links)
- Amphiphysins: Raising the BAR for Synaptic Vesicle Recycling and Membrane Dynamics (Q30039689) (← links)
- Minimization of extracellular space as a driving force in prokaryote association and the origin of eukaryotes (Q30421052) (← links)
- The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies (Q30499359) (← links)
- Cytochemical localization of calcium in prefusion myoblasts from the chick embryo myotome (Q30759558) (← links)
- Developmental regulation of myotonic dystrophy protein kinase in human muscle cells in vitro (Q32062314) (← links)
- Plasticity of the transverse tubules following denervation and subsequent reinnervation in rat slow and fast muscle fibres (Q33195978) (← links)
- Physiological and ultrastructural features of human induced pluripotent and embryonic stem cell-derived skeletal myocytes in vitro (Q33730362) (← links)
- Reversible vacuolation of T-tubules in skeletal muscle: mechanisms and implications for cell biology (Q34075728) (← links)
- The hydrophilic domain of small ankyrin-1 interacts with the two N-terminal immunoglobulin domains of titin (Q34160104) (← links)
- STIM proteins and the endoplasmic reticulum-plasma membrane junctions (Q34183176) (← links)
- Endoplasmic reticulum of animal cells and its organization into structural and functional domains (Q34240633) (← links)
- Abnormal junctions between surface membrane and sarcoplasmic reticulum in skeletal muscle with a mutation targeted to the ryanodine receptor (Q34439884) (← links)
- Molecular organization of transverse tubule/sarcoplasmic reticulum junctions during development of excitation-contraction coupling in skeletal muscle (Q34445587) (← links)
- N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy. (Q34542692) (← links)
- Muscle giants: molecular scaffolds in sarcomerogenesis (Q34793699) (← links)
- Retrograde activation of store-operated calcium channel. (Q35135466) (← links)
- Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle. (Q35760852) (← links)
- Association of calcium channel alpha1S and beta1a subunits is required for the targeting of beta1a but not of alpha1S into skeletal muscle triads (Q36063022) (← links)
- Jagunal is required for reorganizing the endoplasmic reticulum during Drosophila oogenesis (Q36118057) (← links)
- Novel sarco(endo)plasmic reticulum proteins and calcium homeostasis in striated muscles. (Q36227308) (← links)
- Triad formation: organization and function of the sarcoplasmic reticulum calcium release channel and triadin in normal and dysgenic muscle in vitro. (Q36233592) (← links)
- Formation of triads without the dihydropyridine receptor alpha subunits in cell lines from dysgenic skeletal muscle (Q36237030) (← links)
- Coordinated incorporation of skeletal muscle dihydropyridine receptors and ryanodine receptors in peripheral couplings of BC3H1 cells (Q36273983) (← links)
- Abnormal features in skeletal muscle from mice lacking mitsugumin29. (Q36326127) (← links)
- Deficiency of triad junction and contraction in mutant skeletal muscle lacking junctophilin type 1. (Q36376912) (← links)
- Plasma Membrane Repair in Health and Disease (Q36785977) (← links)
- The plasma membrane as a capacitor for energy and metabolism (Q36955222) (← links)
- Assembly and dynamics of proteins of the longitudinal and junctional sarcoplasmic reticulum in skeletal muscle cells (Q37140160) (← links)
- Triadin deletion induces impaired skeletal muscle function (Q37454303) (← links)
- Formation of junctions involved in excitation-contraction coupling in skeletal and cardiac muscle. (Q37463586) (← links)
- Organization of junctional sarcoplasmic reticulum proteins in skeletal muscle fibers. (Q38587629) (← links)
- A guide to the 3D structure of the ryanodine receptor type 1 by cryoEM. (Q38964992) (← links)
- ER-plasma membrane junctions: Why and how do we study them? (Q39336657) (← links)
- Extracellular Ca(2+)-dependent and independent calcium transient in fetal myotubes. (Q39391455) (← links)
- Overexpression of calsequestrin in L6 myoblasts: formation of endoplasmic reticulum subdomains and their evolution into discrete vacuoles where aggregates of the protein are specifically accumulated (Q40387730) (← links)
- Voltage- and ligand-gated ryanodine receptors are functionally separated in developing C2C12 mouse myotubes (Q40876452) (← links)