مورد إلكتروني

226th ENMC International Workshop: : Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20–22 January 2017, Heemskerk, The Netherlands

التفاصيل البيبلوغرافية
العنوان: 226th ENMC International Workshop: : Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20–22 January 2017, Heemskerk, The Netherlands
بيانات النشر: KTH, Systembiologi Elsevier Ltd 2018
تفاصيل مُضافة: Aartsma-Rus, A.
Ferlini, A.
McNally, E. M.
Spitali, P.
Sweeney, H. L.
Al-Khalili Szigyarto, Cristina
Bello, L.
Bronson, A.
Brown, K.
Buccella, F.
Chadwick, J.
Frank, D.
Hoffman, E.
Larkindale, J.
McClorey, G.
Munschauer, R.
Muntoni, F.
Owens, J.
Schara, U.
Straub, V.
Tinsley, J.
Versnel, J.
Vroom, E.
Welch, E.
نوع الوثيقة: Electronic Resource
مستخلص: QC 20220301
مصطلحات الفهرس: Biobank, Biomarker, Duchenne muscular dystrophy, Dystrophin, MRI, alanine aminotransferase, aspartate aminotransferase, biological marker, carbonate dehydratase III, corticosteroid, dysferlin, enolase, fukutin related protein, glucocorticoid receptor, glutamate dehydrogenase, immunoglobulin enhancer binding protein, microRNA, microRNA 133a, microRNA 133b, osteopontin, protein enolase 3, stromelysin, unclassified drug, utrophin, vamorolone, alanine aminotransferase level, aspartate aminotransferase blood level, Becker muscular dystrophy, blood analysis, blood sampling, Conference Paper, corticosteroid therapy, CRISPR-CAS9 system, DNA modification, drug design, exon, exon skipping, gene, gene expression, human, lipidomics, LTBP4 gene, Netherlands, nonhuman, nuclear magnetic resonance imaging, priority journal, protein expression, real time polymerase chain reaction, single nucleotide polymorphism, SPP1 gene, urinalysis, urine sampling, workshop, animal, information dissemination, male, metabolism, non profit organization, validation study, Animals, Biomarkers, Humans, Muscular Dystrophy, Duchenne, Organizations, Nonprofit, Validation Studies as Topic, Cell and Molecular Biology, Cell- och molekylärbiologi, Article in journal, info:eu-repo/semantics/article, text
DOI: 10.1016.j.nmd.2017.10.002
URL: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-282709Test
Neuromuscular Disorders, 0960-8966, 2018, 28:1, s. 77-86
الإتاحة: Open access content. Open access content
info:eu-repo/semantics/restrictedAccess
ملاحظة: English
أرقام أخرى: UPE oai:DiVA.org:kth-282709
0000-0001-6990-1905
doi:10.1016/j.nmd.2017.10.002
PMID 29203356
ISI:000427210600014
Scopus 2-s2.0-85035314174
1235086618
المصدر المساهم: UPPSALA UNIV LIBR
From OAIster®, provided by the OCLC Cooperative.
رقم الانضمام: edsoai.on1235086618
قاعدة البيانات: OAIster