Results 151 to 160 of about 26,568 (204)

Astragaloside IV prevents calpain-1-mediated cardiac hypertrophy and fibrosis induced by diabetes. [PDF]

Front Cardiovasc Med
Zhang Q, Zhao N, Wei S, Lu M, Chen K.
europepmc   +1 more source

Mitofilin Preservation Mitigates Cardiac Injury in Donation-After-Circulatory-Death Hearts. [PDF]

Cells
Chen Q, Kiernan Z, Labate G, Akande O, Lesnefsky EJ, Quader M.   +5 more
europepmc   +1 more source

Retraction Note: Effects of Novel Calpain Inhibitors in Transgenic Animal Model of Parkinson's disease/dementia with Lewy bodies. [PDF]

Sci Rep
Hassen GW, Kesner L, Stracher A, Shulman A, Rockenstein E, Mante M, Adame A, Overk C, Rissman RA, Masliah E.   +9 more
europepmc   +1 more source

Correction: Accumulation of human full-length tau induces degradation of nicotinic acetylcholine receptor α4 via activating calpain-2. [PDF]

Sci Rep
Yin Y, Wang Y, Gao D, Ye J, Wang X, Fang L, Wu D, Pi G, Lu C, Zhou XW, Yang Y, Wang JZ.   +11 more
europepmc   +1 more source

Spirohydantoin derivatives exert dopamine D₂-like receptor-independent cytotoxicity in glioblastoma cells with possible involvement of calpain inhibition. [PDF]

Sci Rep
Kucwaj-Brysz K, Podlewska S, Jakubowska K, Mąsior A, Wilczkowski M, Duszyńska B, Drukała J, Handzlik J, Jantas D.   +8 more
europepmc   +1 more source

Calpain-2 Regulates Kinesin and Dynein Dysfunction in Neurotoxin-Induced Motoneuron Injury. [PDF]

Brain Sci
Zaman V, Green C, Sitgreaves K, Gathings A, Drasites KP, Coleman N, Huell J, McDonald T, Banik NL, Haque A.   +9 more
europepmc   +1 more source

Piezo1 specific deletion in endothelial cell protects the progression of pulmonary fibrosis in mice. [PDF]

Cell Commun Signal
He B, Tan Q, Xu H, Chen X, Wan R, Yao Y, Pan X, Liu S, Chen X, Jiang J, Luo S, An Y, Li J.   +12 more
europepmc   +1 more source

Biphasic regulation of myogenesis by ALDH2, aldosterone, and oxidative stress. [PDF]

Pflugers Arch
Martínez-Cortés JE, Valle-Clara M, Fernández-Hernández D, Ávila G.   +3 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Calpain-3 mutations in Turkey

European Journal of Pediatrics, 2006
Autosomal recessive limb-girdle muscular dystrophies (LGMD2s) are a clinically and genetically heterogeneous group of disorders, characterized by progressive involvement of the proximal limb girdle muscles; the group includes at least 10 different genetic entities.
BALCI B, AURINO S, HALILOGLU G, TALIM B, ERDEM S, AKCOREN Z, TAN E, CAGLAR M, RICHARD I, NIGRO, Vincenzo, TOPALOGLU H, DINCER P.   +11 more
openaire   +3 more sources