المؤلفون: J.-P. Jin, Hongguang Wei, Han Zhong Feng, Stephanie Kern, Steven E. Cala

المصدر: FEBS Open Bio
FEBS Open Bio, Vol 4, Iss C, Pp 11-17 (2014)

مصطلحات موضوعية: Genetically modified mouse, α-SKA, alpha-skeletal muscle actin, Pathology, medicine.medical_specialty, N-terminal truncation, Cardiomyocyte, macromolecular substances, TnT, Troponin T, Article, cTnI, cardiac troponin I, General Biochemistry, Genetics and Molecular Biology, Contractility, 03 medical and health sciences, 0302 clinical medicine, Transgenic mouse, Troponin I, Medicine, cTnI-ND, N-terminal truncated cardiac troponin I, lcsh:QH301-705.5, Actin, 030304 developmental biology, 0303 health sciences, Smooth muscle tissue, Troponin T, business.industry, α-SMA, alpha-smooth muscle actin, α-CA, alpha-cardiac actin, α-SMA, Cell biology, medicine.anatomical_structure, lcsh:Biology (General), Cardiac muscle remodeling, TnI, troponin I, business, Myofibril, 030217 neurology & neurosurgery, Blood vessel

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d2b7e484f28dcbdcd34b2838d57ca89
https://doi.org/10.1016/j.fob.2013.11.002

المؤلفون: Akane Imai, Maiko Haga-Tsujimura, Tomoko Nashida, Sumio Yoshie, Hiromi Shimomura

المصدر: FEBS Open Bio

مصطلحات موضوعية: Messenger RNA, Pathology, medicine.medical_specialty, business.industry, Myoepithelial cell, Skeletal muscle, Nod, macromolecular substances, medicine.disease, Skeletal muscle actin, General Biochemistry, Genetics and Molecular Biology, Article, Parotid gland, medicine.anatomical_structure, Atrophy, stomatognathic system, Diabetic NOD mouse, medicine, Myoepithelial cells, business, Pathological, Actin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3213695086aa1af04f5047d70968c256
http://europepmc.org/articles/PMC3668504

المؤلفون: Tajsharghi, Homa, 1968, Ohlsson, Monica, Palm, L., Oldfors, Anders, 1951

المصدر: Neuromuscular Disorders. 22(11):923-933

مصطلحات موضوعية: Clinical Medicine, Klinisk medicin, Tropomyosin, Myopathy, Nemaline myopathy, Cap disease, Congenital myopathy, Distal, recessive nemaline myopathy, alpha-actin gene, familial hypertrophic, cardiomyopathy, cause distal arthrogryposis, skeletal-muscle actin, nebulin gene, cap disease, congenital myopathy, binding-protein, tpm2

URL الوصول: https://gup.ub.gu.se/publication/168966

المؤلفون: Ludwig, S., Mannherz, Hans Georg, Schmitt, S., Schäffer, Matthias, Zentgraf, Hanswalter, Napirei, Markus

المصدر: The international journal of biochemistry & cell biology

مصطلحات موضوعية: ddc:610, Amino acid sequence, Animal, Cattle, CHROMATIN BREAKDOWN, deoxyribonuclease 1, Deoxyribonuclease I, Electrophoresis, gene expression, glycosylation, Hepatectomy, Humans, I GENE-EXPRESSION, Inbred C57BL, Isoenzymes, LIVER, Male, MALE CD-1 MICE, Messenger, Mice, MOUSE-LIVER, Polyacrylamide gel, RAT, RNA, SECRETORY PROTEINS, SERUM, SKELETAL-MUSCLE ACTIN, SYSTEMIC-LUPUS-ERYTHEMATOSUS, Tissue Distribution

وصف الملف: 1079–1093

Relation: urn:issn:1357-2725

الاتاحة: https://bibliographie.ub.rub.de/entry/70a9ac2d-c1bf-4ec2-99c8-1d2c6fcaddc0

المؤلفون: Ballweber, Edda, Galla, Marco Thomas, Aktories, Klaus, Yeoh, Sharon, Weeds, Alan G., Mannherz, Hans Georg

المصدر: Federation of European Biochemical Societies: FEBS letters

مصطلحات موضوعية: ddc:610, actin binding protein, ADP-ribosylated actin, CAPS, COMPLEX, DNASE-I, ENDS, FILAMENT, FILAMENT TURNOVER, MYOSIN, PERFRINGENS IOTA-TOXIN, POLYMERIZATION, SKELETAL-MUSCLE ACTIN, TURNOVER

وصف الملف: 131–135

Relation: urn:issn:0014-5793

الاتاحة: https://bibliographie.ub.rub.de/entry/cf5ba9f5-5614-4e1a-a6f0-bf51a64761ae

المؤلفون: Roman, William

الاتاحة: http://data.europeana.eu/aggregation/europeana/2048441/item_SBS7JS3EFRA4Z5QABNKMDYGNACEQUPW4