المؤلفون: S. Subramanian, Ajay Taranath, Sniya Sudhakar, Karuna Shekdar, Pradeep Krishnan, Richard J. Leventer, César Augusto Pinheiro Ferreira Alves, Kimberly A. Aldinger, Manohar Shroff, Kshitij Mankad, Filippo Arrigoni, Asthik Biswas, William B. Dobyns

المصدر: AJNR Am J Neuroradiol

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Gyral abnormalities, biology, business.industry, Malformation of cortical development, Pediatrics, Phenotype, Mutation (genetic algorithm), biology.protein, Medicine, ACTA2 gene, Radiology, Nuclear Medicine and imaging, In patient, Neurology (clinical), ACTA2, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c972037010f62de3ba5d925b50def4fTest
https://doi.org/10.3174/ajnr.a7364Test

المؤلفون: Xiao-Li Shao, Wen-Xian Yang, Li Zhao, Yan-Yun Li, Hang-Hu Zhang, Jia-Ni Hu

المصدر: World Journal of Clinical Cases

مصطلحات موضوعية: biology, business.industry, General Medicine, Multi-systemic smooth muscle dysfunction syndrome, Bioinformatics, Gene detection, Smooth muscle, Seizures, Mutation (genetic algorithm), Case report, biology.protein, Medicine, ACTA2 gene, ACTA2, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9516ae6f4d37a2a0236378814242eeffTest
http://europepmc.org/articles/PMC8546807Test

المؤلفون: Kindurytė, Austėja, Petkevičiūtė, Justė

المساهمون: Laužikienė, Dalia

المصدر: Juvenes Pro Medicina 2021 : 17th international and 59th Polish conference, 14-16th May 2021, Łódź, Poland : the book of abstract, Łódź : Medical University of Łódź, 2021, p. 244 ; eISBN 9788394762742

مصطلحات موضوعية: ACTA2 gene, gene mutation, Multisystemic smooth muscle dysfunction syndrome

العلاقة: http://vu.lvb.lt/VU:ELABAPDB93476304&prefLang=en_USTest

الإتاحة: http://vu.lvb.lt/VU:ELABAPDB93476304&prefLang=en_USTest

المؤلفون: Mia, M.M, Bank, R.A

المساهمون: DUKE-NUS MEDICAL SCHOOL

المصدر: Unpaywall 20201031

مصطلحات موضوعية: alpha smooth muscle actin, caffeic acid phenethyl ester, collagen type 1, fibronectin, messenger RNA, Smad2 protein, Smad3 protein, tenascin, transcription factor Gli1, transcription factor Gli2, transcription factor Snail, transcription factor Snail1, transforming growth factor beta1, unclassified drug, ACTA2 protein, human, actin, actin binding protein, caffeic acid derivative, muscle protein, phenethyl alcohol, PLOD2 protein, procollagen lysine 2 oxoglutarate 5 dioxygenase, Smad protein, transcription factor, transgelin, ACTA2 gene, adult, antifibrotic activity, Article

العلاقة: Mia, M.M, Bank, R.A (2016). The pro-fibrotic properties of transforming growth factor on human fibroblasts are counteracted by caffeic acid by inhibiting myofibroblast formation and collagen synthesis. Cell and Tissue Research 363 (3) : 775-789. ScholarBank@NUS Repository. https://doi.org/10.1007/s00441-015-2285-6Test; https://scholarbank.nus.edu.sg/handle/10635/179593Test

الإتاحة: https://doi.org/10.1007/s00441-015-2285-6Test
https://scholarbank.nus.edu.sg/handle/10635/179593Test

المؤلفون: Jiyuan, Chen, Kaveeta, Kaw, Hailong, Lu, Patricia M, Fagnant, Abhijnan, Chattopadhyay, Xue Yan, Duan, Zhen, Zhou, Shuangtao, Ma, Zhenan, Liu, Jian, Huang, Kristine, Kamm, James T, Stull, Callie S, Kwartler, Kathleen M, Trybus, Dianna M, Milewicz

المصدر: The Journal of Biological Chemistry

مصطلحات موضوعية: actin folding, ACTA2, gene for smooth muscle α-actin, MRTF-A, myocardin-related transcription factor-A, Aortic Diseases, Mutation, Missense, SMC, smooth muscle cell, macromolecular substances, TIRF, total internal reflection fluorescence, Mice, SM, smooth muscle, RLC, regulatory light chain, Animals, Point Mutation, HTAD, heritable thoracic aortic disease, ACTA1, gene for skeletal muscle α-actin, Aorta, PE, phenylephrine, aortic disease, Actins, Mice, Inbred C57BL, L-NAME, l-Nω-nitroarginine methyl ester, smooth muscle actin, cardiovascular system, CCT, chaperonin-containing TCP-1, TAC, transverse aortic constriction, Chaperonin Containing TCP-1, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::8f72b0fe94460a8619be7f9e99c052b7Test
https://pubmed.ncbi.nlm.nih.gov/34600884Test

المؤلفون: Serviço de Imagem Médica, Mafalda Pinto, Portugal Centro Hospitalar e Universitário de Coimbra

المصدر: Sinapse. 20:181-183

مصطلحات موضوعية: Genetics, Cellular and Molecular Neuroscience, ACTA2 gene, Neurology (clinical), Disease, Biology, Phenotype

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::7e8e4ab1e4960d5d5e518e763f5d79e4Test
https://doi.org/10.46531/sinapse/cc/200032/2020Test

المؤلفون: J Goldberg, P Kostyk, G P Rajendran, S. Kumaraswami

المصدر: International Journal of Obstetric Anesthesia. 47:103173

مصطلحات موضوعية: Genetics, Anesthesiology and Pain Medicine, Text mining, business.industry, Mutation, Mutation (genetic algorithm), MEDLINE, Humans, Obstetrics and Gynecology, ACTA2 gene, Medicine, business, Actins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e939e532c5da9c97e46a497aca7a27fTest
https://doi.org/10.1016/j.ijoa.2021.103173Test

المؤلفون: Elida Vazquez, Susana Boronat, Angel Sanchez-Montanez, Jose de Grazia, Miguel del Campo, Ignacio Delgado

المصدر: Brain and Development. 39:62-66

مصطلحات موضوعية: Male, 0301 basic medicine, Pathology, medicine.medical_specialty, Urinary system, Biology, medicine.disease_cause, 03 medical and health sciences, Fatal Outcome, Imaging, Three-Dimensional, 0302 clinical medicine, Developmental Neuroscience, Congenital mydriasis, medicine, Humans, ACTA2 gene, Cross Infection, Mutation, Vascular disease, Siblings, Infant, Newborn, Brain, General Medicine, medicine.disease, Magnetic Resonance Imaging, Phenotype, Actins, Hypoplasia, Cerebral Angiography, Cerebrovascular Disorders, 030104 developmental biology, Pediatrics, Perinatology and Child Health, biology.protein, Female, Neurology (clinical), ACTA2, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e17dcf9cab6796eabcf81e35dcb5adTest
https://doi.org/10.1016/j.braindev.2016.08.003Test

المؤلفون: Luis Enrique Lezcano Gort, Zineb Kounka, María Victoria Mogollón Jiménez, Lorenzo Monserrat, Benjamín Roque Rodríguez, José Javier Gómez Barrado

المصدر: Revista espanola de cardiologia (English ed.). 73(4)

مصطلحات موضوعية: Genetics, Adult, Male, Aortic Aneurysm, Thoracic, business.industry, DNA Mutational Analysis, General Medicine, DNA, Actins, Pedigree, Aortic Dissection, New mutation, Mutation, Medicine, ACTA2 gene, Humans, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f53de8edd0baff357be181c28d3c0956Test
https://pubmed.ncbi.nlm.nih.gov/31879232Test

المؤلفون: Andrew Zhang, Karen G Grajewski, Alexandria Jo, John Kim

المصدر: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 46(3)

مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Neuroimaging, Smooth muscle, Medicine, ACTA2 gene, Humans, biology, business.industry, Specific mutation, Brain, General Medicine, Phenotype, Actins, Cerebrovascular imaging, Cerebrovascular Disorders, Neurology, Mutation (genetic algorithm), Mutation, 030221 ophthalmology & optometry, biology.protein, Neurology (clinical), ACTA2, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc74d0560c2994185f0a75d005ff3e2Test
https://pubmed.ncbi.nlm.nih.gov/30975232Test