Peter D. Yurchenco

Rutgers, The State University of New Jersey — United States

Medicine · Health Sciences

69h-index18.0kcitations150works4.52yr avg
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Research Topics

Cell Adhesion Molecules Research(107), Cellular Mechanics and Interactions(38), Muscle Physiology and Disorders(31), Protease and Inhibitor Mechanisms(20), Proteoglycans and glycosaminoglycans research(15)

Publications150 total

Glomerular basement membrane structural integrity dictates trans-tissue deposition of laminin in the kidney
Cell Reports·2026Open Access
Dual AAV amelioration of Lama2-null muscular dystrophy and neuropathy
2026Open Access
Cryo-EM reveals molecular mechanisms underlying the inhibitory effect of netrin-4 on laminin matrix formation
Nature Communications·2025Open Access
Basement Membrane Structural Integrity Dictates Trans-Tissue Deposition of Laminin in Mammals
2025Open Access
Polymerizing laminins in development, health, and disease
Journal of Biological Chemistry·2024· 23 citedOpen Access
European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17–19, 2023, Barcelona, Spain
Neuromuscular Disorders·2024· 4 citedOpen Access
Dual transgene amelioration of Lama2-null muscular dystrophy
Matrix Biology·2023· 4 citedOpen Access
Cryo-EM reveals the molecular basis of laminin polymerization and LN-lamininopathies
Nature Communications·2023· 18 citedOpen Access
Exogenous laminin exhibits a unique vascular pattern in the brain via binding to dystroglycan and integrins
Fluids and Barriers of the CNS·2022· 4 citedOpen Access
Amelioration of muscle and nerve pathology of Lama2-related dystrophy by AAV9-laminin-αLN linker protein
JCI Insight·2022· 20 citedOpen Access
Decision letter: Kidney organoids recapitulate human basement membrane assembly in health and disease
2021Open Access
Merosin deficient congenital muscular dystrophy type 1A: An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands
Neuromuscular Disorders·2021· 6 citedOpen Access
Organization of the laminin polymer node
Matrix Biology·2021· 24 citedOpen Access
CONGENITAL MUSCULAR DYSTROPHIES
Neuromuscular Disorders·2020
A deletion in the N-terminal polymerizing domain of laminin β2 is a new mouse model of chronic nephrotic syndrome
Kidney International·2020· 12 citedOpen Access
A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder
Development·2020· 33 citedOpen Access
Linker Protein Repair of LAMA2 Dystrophic Neuromuscular Basement Membranes
Frontiers in Molecular Neuroscience·2019· 20 citedOpen Access
P.332Effect of linker protein expression on LAMA2-related muscular dystrophy (MDC1A)
Neuromuscular Disorders·2019
Chimeric protein identification of dystrophic, Pierson and other laminin polymerization residues
Matrix Biology·2018· 16 citedOpen Access
Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome
Journal of the American Society of Nephrology·2017· 34 citedOpen Access
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Frequent Co-authors

Holly Colognato(6), David H. T. Harrison(5), Karen K. McKee(5), Shaohua Li(4), Reinhard Fässler(4), Heinz Furthmayr(4), Julian J. O’Rear(4), George C. Ruben(3), William G. Wadsworth(3), Effie C. Tsilibary(3), Aristidis Charonis(3), Johannes C. Schittny(2), Robert E. Burgeson(2), Jürgen Engel(2), Mats Paulsson(2), Rupert Timpl(2), Renato V. Iozzo(2), Mina J. Bissell(2), Attila Braun(2), Bruce L. Patton(2)