Muscle Biology
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- 2024
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Mark
Thrombospondin-4 deletion does not exacerbate muscular dystrophy in β-sarcoglycan-deficient and laminin α2 chain-deficient mice
(
- Contribution to journal › Article
- 2023
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Mark
Inhibition of the serine protease HtrA1 by SerpinE2 suggests an extracellular proteolytic pathway in the control of neural crest migration
(
- Contribution to journal › Article
- 2022
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Mark
Editorial : Extracellular matrix in homeostasis and cancer
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Skeletal muscle regeneration is altered in the R6/2 mouse model of Huntington’s disease
2022) p.1-23(
- Working paper/Preprint › Preprint in preprint archive
- 2021
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Mark
A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers-Danlos syndrome that proved to be a COL1-related overlap disorder
(
- Contribution to journal › Article
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Mark
A guide to the composition and functions of the extracellular matrix
(
- Contribution to journal › Article
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Mark
Isolated lumbar extension resistance exercise in limited range of motion for patients with lumbar radiculopathy and disk herniation—clinical outcome and influencing factors
(
- Contribution to journal › Article
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Mark
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant : Elucidating its Role in Collagen VI-related Myopathies
(
- Contribution to journal › Article
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Mark
Merosin deficient congenital muscular dystrophy type 1A : An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands
(
- Contribution to journal › Article
- 2020
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Mark
A Family of Laminin α2 Chain-Deficient Mouse Mutants : Advancing the Research on LAMA2-CMD
(
- Contribution to journal › Scientific review
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Mark
Antioxidants reduce muscular dystrophy in the dy2J/dy2J mouse model of laminin α2 chain-deficient muscular dystrophy
(
- Contribution to journal › Article
- 2019
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Mark
A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene
(
- Contribution to journal › Letter
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Mark
Effects of N-acetyl-L-cysteine and vitamin E on congenital muscular dystrophy type 1A disease progression in mice
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
- 2018
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Mark
Laminin α1 reduces muscular dystrophy in dy2Jmice
(
- Contribution to journal › Article
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Mark
Effects of metformin on congenital muscular dystrophy type 1A disease progression in mice: a gender impact study
2018) In Scientific Reports(
- Contribution to journal › Article
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Mark
Potential therapies and biomarkers for LAMA2-CMD. Does the microRNA hype deliver?
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Exploratory Profiling of Urine MicroRNAs in the dy2J/dy2J Mouse Model of LAMA2-CMD : Relation to Disease Progression
(
- Contribution to journal › Article
- 2017
-
Mark
Potent pro-inflammatory and profibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chaindeficient muscular dystrophy
(
- Contribution to journal › Article
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Mark
Bioenergetic Impairment in Congenital Muscular Dystrophy Type 1A and Leigh Syndrome Muscle Cells
(
- Contribution to journal › Article
-
Mark
Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMD
(
- Contribution to journal › Article
- 2016
-
Mark
Bortezomib Does Not Reduce Muscular Dystrophy in the dy2J/dy2J Mouse Model of Laminin α2 Chain-Deficient Muscular Dystrophy.
(
- Contribution to journal › Article
-
Mark
Skeletal muscle wasting and renewal : a pivotal role of myokine IL-6
(
- Contribution to journal › Scientific review
-
Mark
Update on hereditary colorectal cancer
(
- Contribution to journal › Scientific review
-
Mark
Congenital muscular dystrophy with laminin α2 chain-deficiency. Initiation of disease and development of treatment
2016)(
- Thesis › Doctoral thesis (compilation)
- 2015
-
Mark
Deletion of integrin α7 subunit does not aggravate the phenotype of laminin α2 chain-deficient mice.
(
- Contribution to journal › Article
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Mark
Dystrophin deficiency reduces atherosclerotic plaque development in ApoE-null mice.
(
- Contribution to journal › Article
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Mark
Laminin-α2 Chain-Deficient Congenital Muscular Dystrophy: Pathophysiology and Development of Treatment.
(
- Contribution to journal › Article
- 2014
-
Mark
Bortezomib Partially Improves Laminin α2 Chain-Deficient Muscular Dystrophy.
(
- Contribution to journal › Article
-
Mark
Laminin α2 Chain-Deficiency is Associated with microRNA Deregulation in Skeletal Muscle and Plasma.
(
- Contribution to journal › Article
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Mark
Fibrin binds to collagen and provides a bridge for alpha V beta 3 integrin-dependent contraction of collagen gels
(
- Contribution to journal › Article
-
Mark
Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation and increased expression of extracellular matrix proteins in laminin α2 chain-deficient muscle.
(
- Contribution to journal › Article
-
Mark
Loss of Dystrophin and β-Sarcoglycan, Respectively, Significantly Exacerbates the Phenotype of Laminin α2 Chain-Deficient Animals.
(
- Contribution to journal › Article
-
Mark
Caracterización molecular de cáncer colorrectal hereditario en Perú
2014) In Revista de gastroenterología del Perú : órgano oficial de la Sociedad de Gastroenterología del Perú 34(4). p.299-303(
- Contribution to journal › Article
- 2013
-
Mark
Isobaric Tagging-Based Quantification for Proteomic Analysis: A Comparative Study of Spared and Affected Muscles from mdx Mice at the Early Phase of Dystrophy
(
- Contribution to journal › Article
-
Mark
Evaluation of macroporous blood and plasma scaffolds for skeletal muscle tissue engineering
(
- Contribution to journal › Article
-
Mark
Mutation spectrum in South American Lynch syndrome families
(
- Contribution to journal › Article
- 2012
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Mark
Increased Neointimal Thickening in Dystrophin-Deficient mdx Mice.
(
- Contribution to journal › Article
-
Mark
Guidelines for the use and interpretation of assays for monitoring autophagy
(
- Contribution to journal › Scientific review
-
Mark
Cell-matrix interactions in muscle disease.
(
- Contribution to journal › Article
-
Mark
Laminin-211 in skeletal muscle function.
(
- Contribution to journal › Article
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Mark
Oxidized Dextran as Crosslinker for Chitosan Cryogel Scaffolds and Formation of Polyelectrolyte Complexes between Chitosan and Gelatin.
(
- Contribution to journal › Article
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Mark
Porous protein-based scaffolds prepared through freezing as potential scaffolds for tissue engineering.
(
- Contribution to journal › Article
- 2011
-
Mark
Transgenic Expression of Laminin α1 Chain Does Not Prevent Muscle Disease in the mdx Mouse Model for Duchenne Muscular Dystrophy.
(
- Contribution to journal › Article
-
Mark
Proteasome Inhibition Improves the Muscle of Laminin {alpha}2 Chain Deficient Mice.
(
- Contribution to journal › Article
-
Mark
Autophagy is increased in laminin {alpha}2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.
(
- Contribution to journal › Article
-
Mark
Laminin isoforms in atherosclerotic arteries from mice and man.
(
- Contribution to journal › Article
-
Mark
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.
(
- Contribution to journal › Article
- 2010
-
Mark
Transgenic overexpression of laminin 1 chain in laminin 2 chain-deficient mice rescues the disease throughout the lifespan
(
- Contribution to journal › Article
-
Mark
Laminins.
(
- Contribution to journal › Article
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Mark
Distinct roles for laminin globular domains in laminin alpha1 chain mediated rescue of murine laminin alpha2 chain deficiency.
(
- Contribution to journal › Article
- 2009
-
Mark
Gene expression studies of pregastrulation development: the basement membrane is essential for cell differentiation
(
- Thesis › Doctoral thesis (compilation)
-
Mark
E3 domain of laminin alpha 1 chain that binds to dystroglycan is not essential for survival and muscle regeneration in laminin alpha 1 chain mediated correction of laminin alpha 2 chain deficiency
2009) 14th International Congress of the World-Muscle-Society In Neuromuscular Disorders 19(8-9). p.598-599(
- Contribution to journal › Published meeting abstract
-
Mark
Intracellular signaling pathway alterations in laminin alpha 2 chain deficient skeletal muscle and brain
2009) 14th International Congress of the World-Muscle-Society In Neuromuscular Disorders 19(8-9). p.574-574(
- Contribution to journal › Published meeting abstract
-
Mark
Substantial improvement of laminin alpha 2 chain deficiency by laminin alpha 1 chain overexpression persists throughout life
2009) 14th International Congress of the World-Muscle-Society In Neuromuscular Disorders 19(8-9). p.618-618(
- Contribution to journal › Published meeting abstract
-
Mark
Laminin alpha1 domains LG4-5 are essential for the complete differentiation of visceral endoderm.
(
- Contribution to journal › Article
-
Mark
Low-dose busulphan conditioning and neonatal stem cell transplantation preserves vision and restores hematopoiesis in severe murine osteopetrosis.
(
- Contribution to journal › Article
-
Mark
Intrinsic laryngeal muscles are spared from degeneration in the dy(3k)/dy(3k) mouse model of congenital muscular dystrophy type 1A.
(
- Contribution to journal › Article
- 2008
-
Mark
Cib2 binds integrin a7Bb1D and is reduced in laminin a2 chain deficient muscular dystrophy
(
- Contribution to journal › Article
-
Mark
Studies of laminin a2 chain deficient mice -muscle sparing, charaterization of Cib2 and defective spermatorgenesis
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Distinct roles of integrins alpha 6 and alpha 4 in fetal liver hematopoietic stem and progenitor cell homing
(
- Contribution to journal › Published meeting abstract
-
Mark
Gain-of-function induced defects by PITX2 in eye and limb development
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Novel expression and transcriptional regulation of FoxJ1 during oro-facial morphogenesis
(
- Contribution to journal › Article
-
Mark
The major basement membrane components localize to the chondrocyte pericellular matrix - A cartilage basement membrane equivalent?
(
- Contribution to journal › Article
-
Mark
Gene Expression in mESC Deficient in FGFR Signalling and the Identification of the Novel Gene Ened
(
- Thesis › Doctoral thesis (compilation)
-
Mark
Expression of the novel gene Ened during mouse and Xenopus embryonic development.
(
- Contribution to journal › Article
-
Mark
PITX2 gain-of-function induced defects in mouse forelimb development.
(
- Contribution to journal › Article
- 2007
-
Mark
Distinct roles of integrins {alpha}6 and {alpha}4 in homing of fetal liver hematopoietic stem and progenitor cells.
(
- Contribution to journal › Article
-
Mark
Dystroglycan: a possible mediator for reducing congenital muscular dystrophy?
(
- Contribution to journal › Scientific review
-
Mark
Laminin isoforms in development and disease.
(
- Contribution to journal › Scientific review
-
Mark
Role of the extracellular matrix and its receptors in smooth muscle cell function: implications in vascular development and disease
(
- Contribution to journal › Scientific review
-
Mark
Gene expression profiling of differentiating embryonic stem cells expressing dominant negative fibroblast growth factor receptor 2.
(
- Contribution to journal › Article
-
Mark
Compositional differences between infant and adult human corneal basement membranes
(
- Contribution to journal › Article
- 2006
-
Mark
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy.
(
- Contribution to journal › Article
-
Mark
Laminins in blood vessel development and disease -functional aspects in angiogenesis, atherosclerosis, and muscular dystrophy
2006)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitis.
(
- Contribution to journal › Article
-
Mark
Extraocular muscle is spared upon complete laminin alpha2 chain deficiency: Comparative expression of laminin and integrin isoforms.
(
- Contribution to journal › Article
-
Mark
Monoclonal anti-mouse laminin antibodies: AL-1 reacts with laminin alpha1 chain, AL-2 with laminin beta1 chain, and AL-4 with the coiled-coil domain of laminin beta1 chain.
(
- Contribution to journal › Article
-
Mark
Laminins and Congenital Muscular Dystrophy - From a Mouse Model to Gene Therapy of Laminin alpha2 chain deficiency?
2006)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Laminin alpha1 chain mediated reduction of laminin alpha2 chain deficient muscular dystrophy involves integrin alpha7beta1 and dystroglycan.
(
- Contribution to journal › Article
- 2005
-
Mark
Laminin {alpha}1 Chain Corrects Male Infertility Caused by Absence of Laminin {alpha}2 Chain.
(
- Contribution to journal › Article
-
Mark
Distinctive functions of membrane type 1 matrix-metalloprotease (MT1-MMP or MMP-14) in lung and submandibular gland development are independent of its role in pro-MMP-2 activation
(
- Contribution to journal › Article
- 2004
-
Mark
Amperometric monitoring of redox activity in living yeast cells: comparison of menadione and menadione sodium bisulfite as electron transfer mediators
(
- Contribution to journal › Article
-
Mark
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice.
(
- Contribution to journal › Article
-
Mark
Specific detection of L-glutamate in food using flow-injection analysis and enzymatic recycling of substrate
(
- Contribution to journal › Article
- 2002
-
Mark
Nulp1, a novel basic helix-loop-helix protein expressed broadly during early embryonic organogenesis and prominently in developing dorsal root ganglia.
(
- Contribution to journal › Article
-
Mark
Highly sensitive microfluidic enzyme immunoassay based on immobilised affinity proteins and chemiluminescence detection
2002) 15th International Symposium on Microscale Separations and Analysis(
- Contribution to conference › Paper, not in proceeding