Search Results - "Burkin DJ"

A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.

Authors: Nejati, Parham Falsafi, Nafiseh Alimoradi, Elham et al.

Source: BMC Medical Genomics. 11/4/2025, Vol. 18 Issue 1, p1-9. 9p.

Microenvironment-driven satellite cell regeneration and repair in aging-related sarcopenia: mechanisms and therapeutic frontiers.

Authors: Li, Na Chen, Yushu Wang, Qiong et al.

Source: Stem Cell Research & Therapy. 10/7/2025, Vol. 16 Issue 1, p1-18. 18p.

Transcriptomic profiling of skeletal muscle in the DMD^mdx rat model of Duchenne muscular dystrophy.

Authors: Gorji, Abdolvahab Ebrahimpour Kliczkowska, Katarzyna Ollik, Marcin et al.

Source: Scientific Reports. 8/11/2025, Vol. 15 Issue 1, p1-18. 18p.

Force-dependent development of the myodural bridge in rats: The impact of Integrin α7.

Authors: Zhang, Lu Liu, Yun-Feng Luo, Mi et al.

Source: PLoS ONE. 8/4/2025, Vol. 20 Issue 8, p1-19. 19p.

Tenascin-C orchestrates radiotherapy-induced head and neck tumor regression.

Authors: Loustau T Mitrentsi I Wang N et al.

Source: EMBO molecular medicine [EMBO Mol Med] 2026 May; Vol. 18 (5), pp. 1707-1743. Date of Electronic Publication: 2026 Mar 31.

Publication Type: Journal Article

Journal Info: Publisher: EMBO Press Country of Publication: Germany NLM ID: 101487380 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1757-4684 (Electronic) Linking ISSN: 17574676 NLM ISO Abbreviation: EMBO Mol Med Subsets: MEDLINE

Muscle transcriptome profiling reveals novel molecular pathways and biomarkers in laminin-α2 deficient patients.

Authors: Pini V Catapano F Bonaccorso R et al.

Source: Acta neuropathologica communications [Acta Neuropathol Commun] 2026 Feb 03; Vol. 14 (1). Date of Electronic Publication: 2026 Feb 03.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Electronic Cited Medium: Internet ISSN: 2051-5960 (Electronic) Linking ISSN: 20515960 NLM ISO Abbreviation: Acta Neuropathol Commun Subsets: MEDLINE

Semaglutide restores astrocyte–vascular interactions and blood–brain barrier integrity in a model of diet-induced metabolic syndrome.

Authors: Estato, Vanessa Obadia, Nathalie Chateaubriand, Paulo Henrique et al.

Source: Diabetology & Metabolic Syndrome. 1/4/2025, Vol. 17 Issue 1, p1-16. 16p.

A 5-year natural history study in LAMA2-related muscular dystrophy and SELENON-related myopathy: the Extended LAST STRONG study.

Authors: de Laat, E. C. M. Houwen- van Opstal, S.L.S. Bouman, K. et al.

Source: BMC Neurology. 12/16/2024, Vol. 24 Issue 1, p1-11. 11p.

Systemic inhibition of bone morphogenetic protein 1.3 as a possible treatment for laminin-related congenital muscular dystrophy.

Authors: Matic Jelic I Stokovic N Ivanjko N et al.

Source: International orthopaedics [Int Orthop] 2025 Jan; Vol. 49 (1), pp. 45-52. Date of Electronic Publication: 2024 Dec 02.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7705431 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-5195 (Electronic) Linking ISSN: 03412695 NLM ISO Abbreviation: Int Orthop Subsets: MEDLINE

Sil1-deficient fibroblasts generate an aberrant extracellular matrix leading to tendon disorganisation in Marinesco-Sjögren syndrome.

Authors: Amodei, Laura Ruggieri, Anna Giulia Potenza, Francesca et al.

Source: Journal of Translational Medicine. 8/23/2024, Vol. 22 Issue 1, p1-16. 16p.

CAR T-Cell Therapy for Relapsed/Refractory Diffuse Large B-Cell Lymphoma with Progressive Muscular Dystrophy: A Case Report.

Authors: Chen, Liting Xu, Bin Liu, Wanying et al.

Source: OncoTargets & Therapy. Apr2022, Vol. 15, p361-366. 6p.

Valproic acid reduces muscle susceptibility to contraction‐induced functional loss but increases weakness in two murine models of Duchenne muscular dystrophy.

Authors: Moutachi, Dylan Lemaitre, Mégane Delacroix, Clément et al.

Source: Clinical & Experimental Pharmacology & Physiology. Sep2023, Vol. 50 Issue 9, p749-756.

Learning, memory and blood–brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140.

Authors: Verhaeg, Minou Adamzek, Kevin van de Vijver, Davy et al.

Source: Genes, Brain & Behavior. Jun2024, Vol. 23 Issue 3, p1-12. 12p.

Cardiorespiratory fitness and the association with galectin-1 in middle-aged individuals.

Authors: Arvidsson, Daniel Rodrigues Silva, Vagner Ramon Ekblom, Örjan et al.

Source: PLoS ONE. 4/5/2024, Vol. 19 Issue 4, p1-9. 9p.

Vemurafenib improves muscle histopathology in a mouse model of LAMA2-related congenital muscular dystrophy.

Authors: Oliveira-Santos A Dagda M Wittmann J et al.

Source: Disease models & mechanisms [Dis Model Mech] 2023 Jun 01; Vol. 16 (6). Date of Electronic Publication: 2023 May 10.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Company of Biologists Ltd Country of Publication: England NLM ID: 101483332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1754-8411 (Electronic) Linking ISSN: 17548403 NLM ISO Abbreviation: Dis Model Mech Subsets: MEDLINE

Mesothelioma cells breaking bad: loss of integrin α7 promotes cell motility and poor clinical outcomes in patients.

Authors: Burkin DJ Fontelonga TM

Source: The Journal of pathology [J Pathol] 2015 Nov; Vol. 237 (3), pp. 282-4. Date of Electronic Publication: 2015 Aug 26.

Publication Type: Journal Article; Comment

Journal Info: Publisher: John Wiley And Sons Country of Publication: England NLM ID: 0204634 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-9896 (Electronic) Linking ISSN: 00223417 NLM ISO Abbreviation: J Pathol Subsets: MEDLINE

Centre-based landscape of muscular dystrophies in Gujarat: insight into genetic diagnosis and management.

Authors: Sindhav, Gaurang Trivedi, Pooja Patel, Krishnakumari et al.

Source: Journal of Rare Diseases. 7/22/2025, Vol. 4 Issue 1, p1-13. 13p.

Valproate independently activates Snf1, inhibits TORC1, and induces repression of INO1 transcription by increasing nuclear localization of Opi1.

Authors: Case, Kendall C. Orkun, Lara Greenberg, Miriam L.

Source: Scientific Reports. 7/9/2025, Vol. 15 Issue 1, p1-26. 26p.

A gene therapy approach for the treatment of limb-girdle muscular dystrophy 2C/R5.

Authors: Hermann H Wuebbles RD Burkin DJ

Source: Molecular therapy. Methods & clinical development [Mol Ther Methods Clin Dev] 2023 Mar 30; Vol. 29, pp. 160-161. Date of Electronic Publication: 2023 Mar 30 (Print Publication: 2023).

Publication Type: News

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 101624857 Publication Model: eCollection Cited Medium: Print ISSN: 2329-0501 (Print) Linking ISSN: 23290501 NLM ISO Abbreviation: Mol Ther Methods Clin Dev Subsets: PubMed not MEDLINE

The alpha7 integrin subunit in astrocytes promotes endothelial blood-brain barrier integrity.

Authors: Chen Z Kelly JR Morales JE et al.

Source: Development (Cambridge, England) [Development] 2023 Mar 15; Vol. 150 (6). Date of Electronic Publication: 2023 Mar 24.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

Journal Info: Publisher: Company Of Biologists Limited Country of Publication: England NLM ID: 8701744 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-9129 (Electronic) Linking ISSN: 09501991 NLM ISO Abbreviation: Development Subsets: MEDLINE