| scholarly article | Q13442814 |
| P50 | author | Li Xu | Q95646405 |
| Nirakar Sahoo | Q41817642 | ||
| Renzhi Han | Q57020595 | ||
| Qiong Gao | Q57379525 | ||
| Yue Zhuo | Q57379578 | ||
| P2093 | author name string | Xiang Wang | |
| Haoxing Xu | |||
| Xiaoli Zhang | |||
| Xinran Li | |||
| Xiping Cheng | |||
| Marc Ferrer | |||
| Mohammad Ali Samie | |||
| Abigail G Garrity | |||
| James Dowling | |||
| Libing Dong | |||
| Wai Lok Tsang | |||
| Marlene Azar | |||
| P2860 | cites work | Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel | Q24290404 |
| Neurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IV | Q24655743 | ||
| Membrane repair redux: redox of MG53 | Q83144922 | ||
| Defective membrane repair in dysferlin-deficient muscular dystrophy | Q28203095 | ||
| Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin | Q28241932 | ||
| TPC proteins are phosphoinositide- activated sodium-selective ion channels in endosomes and lysosomes | Q28276964 | ||
| The type IV mucolipidosis-associated protein TRPML1 is an endolysosomal iron release channel | Q28294133 | ||
| Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation | Q28507844 | ||
| Impaired membrane resealing and autoimmune myositis in synaptotagmin VII-deficient mice | Q28511824 | ||
| MG53 nucleates assembly of cell membrane repair machinery. | Q28511885 | ||
| Plasma membrane repair is mediated by Ca(2+)-regulated exocytosis of lysosomes | Q28572060 | ||
| PI(3,5)P2 controls membrane trafficking by direct activation of mucolipin Ca2+ release channels in the endolysosome | Q29543488 | ||
| Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy | Q30545559 | ||
| Dysferlin and the plasma membrane repair in muscular dystrophy | Q33201061 | ||
| A role for calmodulin in organelle membrane tubulation | Q34449992 | ||
| Disruptions of muscle fiber plasma membranes. Role in exercise-induced damage | Q35831693 | ||
| Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. | Q36273863 | ||
| Repair of injured plasma membrane by rapid Ca2+-dependent endocytosis | Q36491740 | ||
| Molecular mechanisms of muscular dystrophies: old and new players | Q36593241 | ||
| The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy | Q36842039 | ||
| Caveolae internalization repairs wounded cells and muscle fibers. | Q37181157 | ||
| A TRP channel in the lysosome regulates large particle phagocytosis via focal exocytosis | Q37224430 | ||
| Cognitive dysfunction and depression in Fabry disease: a systematic review | Q38129244 | ||
| Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. | Q40612428 | ||
| Lipid storage disorders block lysosomal trafficking by inhibiting a TRP channel and lysosomal calcium release | Q41822869 | ||
| v-SNARE composition distinguishes synaptic vesicle pools. | Q42142233 | ||
| Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy. | Q42576112 | ||
| Gene delivery to muscle | Q46092237 | ||
| Chaperone-mediated autophagy is defective in mucolipidosis type IV. | Q46178880 | ||
| LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. | Q47375901 | ||
| ESCRT machinery is required for plasma membrane repair | Q50462403 | ||
| Loss of cytoplasmic basic fibroblast growth factor from physiologically wounded myofibers of normal and dystrophic muscle. | Q52515753 | ||
| Muscle fiber types: how many and what kind? | Q54171280 | ||
| Muscle involvement in mucolipidosis IV | Q68679385 | ||
| A muscle disorder as presenting symptom in a child with mucolipidosis IV | Q71805065 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1187-1192 | |
| P577 | publication date | 2014-09-14 | |
| P1433 | published in | Nature Medicine | Q1633234 |
| P1476 | title | The intracellular Ca²⁺ channel MCOLN1 is required for sarcolemma repair to prevent muscular dystrophy | |
| P478 | volume | 20 |
| Q28546097 | A Fine Balance of Dietary Lipids Improves Pathology of a Murine Model of VCP-Associated Multisystem Proteinopathy |
| Q38828599 | A fragmented form of annexin A1 is secreted from C2C12 myotubes by electric pulse-induced contraction |
| Q42571327 | A melanosomal two-pore sodium channel regulates pigmentation |
| Q38788245 | A molecular mechanism to regulate lysosome motility for lysosome positioning and tubulation. |
| Q28084142 | Above the fray: Surface remodeling by secreted lysosomal enzymes leads to endocytosis-mediated plasma membrane repair |
| Q41189322 | BK channel agonist represents a potential therapeutic approach for lysosomal storage diseases |
| Q28392384 | Biphasic regulation of lysosomal exocytosis by oxidative stress |
| Q90613869 | Calcium Dyshomeostasis and Lysosomal Ca2+ Dysfunction in Amyotrophic Lateral Sclerosis |
| Q38620889 | Calcium signaling in membrane repair |
| Q90102755 | Cardiomyocyte damage control in heart failure and the role of the sarcolemma |
| Q59286326 | Cellular mechanisms and signals that coordinate plasma membrane repair |
| Q35738899 | Chronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin-/- Mice |
| Q49914916 | Co-deficiency of Lysosomal Mucolipins 3 and 1 in Cochlear Hair Cells Diminishes Outer Hair Cell Longevity and Accelerates Age-Related Hearing Loss. |
| Q47438098 | Cryo-EM structures of the human endolysosomal TRPML3 channel in three distinct states |
| Q37623318 | Fusion of lysosomes with secretory organelles leads to uncontrolled exocytosis in the lysosomal storage disease mucolipidosis type IV. |
| Q38721360 | Inhibition of Transient Receptor Potential Channel Mucolipin-1 (TRPML1) by Lysosomal Adenosine Involved in Severe Combined Immunodeficiency Diseases |
| Q51536571 | Lysosomal Ca2+ Signaling is Essential for Osteoclastogenesis and Bone Remodeling. |
| Q47124126 | Lysosomal Calcium in Neurodegeneration |
| Q34462083 | Lysosomal physiology |
| Q36146335 | Membrane Repair: Mechanisms and Pathophysiology. |
| Q36372961 | Membrane fusion in muscle development and repair |
| Q52373051 | Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet. |
| Q50441194 | Novel degenerative and developmental defects in a zebrafish model of mucolipidosis type IV. |
| Q35691118 | Organellar channels and transporters |
| Q35974137 | Plasma Membrane Repair Is Regulated Extracellularly by Proteases Released from Lysosomes. |
| Q38781697 | ROS and intracellular ion channels |
| Q38534629 | Regulation of heme biosynthesis and transport in metazoa |
| Q47740081 | Robust lysosomal calcium signaling through channel TRPML1 is impaired by lysosomal lipid accumulation. |
| Q35035202 | Role of TRP channels in the cardiovascular system |
| Q35141257 | S100 and annexin proteins identify cell membrane damage as the Achilles heel of metastatic cancer cells |
| Q90016689 | Small-molecule activation of lysosomal TRP channels ameliorates Duchenne muscular dystrophy in mouse models |
| Q47035965 | Structure of mammalian endolysosomal TRPML1 channel in nanodiscs |
| Q90411079 | TRPML Cation Channels in Inflammation and Immunity |
| Q90127695 | TRPML1 and RAS-driven cancers - exploring a link with great therapeutic potential |
| Q91854257 | TRPML1 links lysosomal calcium to autophagosome biogenesis through the activation of the CaMKKβ/VPS34 pathway |
| Q38870984 | The Phosphoinositide-Gated Lysosomal Ca(2+) Channel, TRPML1, Is Required for Phagosome Maturation |
| Q47224732 | The lysosomal Ca2+ release channel TRPML1 regulates lysosome size by activating calmodulin |
| Q52756417 | Treating pediatric neuromuscular disorders: The future is now. |
| Q34551759 | Two-Pore Channels: Catalyzers of Endolysosomal Transport and Function. |
| Q92721361 | Two-pore channels regulate Tat endolysosome escape and Tat-mediated HIV-1 LTR transactivation |
| Q27334518 | VAMP7 regulates constitutive membrane incorporation of the cold-activated channel TRPM8. |
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