| P50 | author | Bryan D. Crawford | Q41191609 |
| P2093 | author name string | Clarissa A Henry | |
| | Michelle F Goody | |
| | Andre Khalil | |
| | Meghan W Kelly | |
| | Christine J Reynolds | |
| P2860 | cites work | Nicotinamide riboside kinase structures reveal new pathways to NAD+ | Q21145891 |
| | p53 activation by knockdown technologies | Q21563456 |
| | Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE | Q24301093 |
| | Spatial and temporal expression of the beta1D integrin during mouse development | Q24316487 |
| | Mutations in the integrin alpha7 gene cause congenital myopathy | Q24317420 |
| | A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity | Q24321993 |
| | Absence of integrin alpha 7 causes a novel form of muscular dystrophy | Q24323372 |
| | Integrin ligands at a glance | Q24600618 |
| | Paxillin comes of age | Q24657852 |
| | The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy | Q24681141 |
| | Nicotinamide protects against ethanol-induced apoptotic neurodegeneration in the developing mouse brain | Q25255947 |
| | Time-lapse analysis and mathematical characterization elucidate novel mechanisms underlying muscle morphogenesis | Q27313686 |
| | Stages of embryonic development of the zebrafish | Q27860947 |
| | Discoveries of nicotinamide riboside as a nutrient and conserved NRK genes establish a Preiss-Handler independent route to NAD+ in fungi and humans | Q27937147 |
| | Dystroglycan is a binding protein of laminin and merosin in peripheral nerve | Q28238540 |
| | Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study | Q28238656 |
| | Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor | Q28254849 |
| | Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix | Q28296676 |
| | Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy | Q28297222 |
| | Integrin alpha6beta1-laminin interactions regulate early myotome formation in the mouse embryo | Q28505714 |
| | The adaptor protein paxillin is essential for normal development in the mouse and is a critical transducer of fibronectin signaling | Q28589349 |
| | Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice | Q28590908 |
| | Ral-regulated interaction between Sec5 and paxillin targets Exocyst to focal complexes during cell migration | Q30393951 |
| | Dynamic formation of microenvironments at the myotendinous junction correlates with muscle fiber morphogenesis in zebrafish | Q30486454 |
| | Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan | Q30489039 |
| | The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment | Q30490034 |
| | Zebrafish orthologs of human muscular dystrophy genes | Q33279472 |
| | Drug screening in a zebrafish model of Duchenne muscular dystrophy. | Q33845739 |
| | Influence of nicotinic acid on serum cholesterol in man. | Q33972172 |
| | Niaspan treatment induces neuroprotection after stroke | Q34079520 |
| | An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy. | Q34091913 |
| | The muscle integrin binding protein (MIBP) interacts with alpha7beta1 integrin and regulates cell adhesion and laminin matrix deposition | Q34225519 |
| | Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities | Q34329257 |
| | Bridging structure with function: structural, regulatory, and developmental role of laminins | Q34582955 |
| | Zebrafish Fukutin family proteins link the unfolded protein response with dystroglycanopathies | Q34766986 |
| | A dystroglycan mutation associated with limb-girdle muscular dystrophy. | Q34767085 |
| | Controlling morpholino experiments: don't stop making antisense. | Q34769101 |
| | Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin-ECM adhesion complex | Q34774115 |
| | Transgenic expression of {alpha}7{beta}1 integrin maintains muscle integrity, increases regenerative capacity, promotes hypertrophy, and reduces cardiomyopathy in dystrophic mice | Q35083511 |
| | Activity and distribution of paxillin, focal adhesion kinase, and cadherin indicate cooperative roles during zebrafish morphogenesis | Q35670172 |
| | Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy | Q35952091 |
| | Characterization of the laminin gene family and evolution in zebrafish. | Q51891008 |
| | Laminins, via heparan sulfate proteoglycans, participate in zebrafish myotome morphogenesis by modulating the pattern of Bmp responsiveness. | Q51894650 |
| | Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice. | Q52200996 |
| | Soft substrates drive optimal differentiation of human healthy and dystrophic myotubes. | Q53295077 |
| | Intramuscular degeneration process in Duchenne muscular dystrophy--investigation by longitudinal MR imaging of the skeletal muscles | Q68202880 |
| | Alpha 6 integrin distribution in human embryonic and adult tissues | Q72050139 |
| | Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin | Q83309941 |
| | Alpha 6 integrin is important for myogenic stem cell differentiation | Q84565378 |
| | A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. | Q36232550 |
| | Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin | Q37089639 |
| | Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy | Q37194805 |
| | Enhancing cardiovascular disease risk reduction: raising high-density lipoprotein levels. | Q37539675 |
| | Direct effects of the pathogenic mutation on satellite cell function in muscular dystrophy | Q37764976 |
| | Dystroglycanopathies: coming into focus | Q37852376 |
| | Magnetic resonance imaging of skeletal muscle in patients with Duchenne muscular dystrophy--serial axial and sagittal section studies | Q41895993 |
| | Overexpression of mini-agrin in skeletal muscle increases muscle integrity and regenerative capacity in laminin-alpha2-deficient mice. | Q42478963 |
| | Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dy(W) mouse model of merosin-deficient congenital muscular dystrophy type 1A. | Q42489627 |
| | Nrk2b-mediated NAD+ production regulates cell adhesion and is required for muscle morphogenesis in vivo: Nrk2b and NAD+ in muscle morphogenesis | Q42568079 |
| | Paxillin isoforms in mouse. Lack of the gamma isoform and developmentally specific beta isoform expression. | Q42827022 |
| | Niacin improves renal lipid metabolism and slows progression in chronic kidney disease | Q43251558 |
| | Extracellular matrix components direct porcine muscle stem cell behavior | Q43255771 |
| | CD117-positive cells in adult human heart are localized in the subepicardium, and their activation is associated with laminin-1 and alpha6 integrin expression | Q44775190 |
| | Combined haploid and insertional mutation screen in the zebrafish | Q45184325 |
| | Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice | Q45876189 |
| | Genes required for functional glycosylation of dystroglycan are conserved in zebrafish | Q46480449 |
| | Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos. | Q47073130 |
| | Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva. | Q47073234 |
| | Zebrafish mutants identify an essential role for laminins in notochord formation. | Q48297604 |
| | Poly(ADP-ribose) polymerase gene disruption renders mice resistant to cerebral ischemia | Q48616927 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | muscular dystrophy | Q1137767 |
| | Danio rerio | Q169444 |
| | Laminin, gamma 1 | Q29829508 |
| P304 | page(s) | e1001409 | |
| P577 | publication date | 2012-10-23 | |
| P1433 | published in | PLOS Biology | Q1771695 |
| P1476 | title | NAD+ biosynthesis ameliorates a zebrafish model of muscular dystrophy | |
| P478 | volume | 10 | |