يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"Truncated FUS protein expression"', وقت الاستعلام: 0.63s تنقيح النتائج
  1. 1
    دورية أكاديمية
    The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment

    المؤلفون: Lanteri P., Meola I., Canosa A., De Marco G., Lomartire A., Rinaudo M. T., Albamonte E., Sansone V. A., Lunetta C., Manera U., Vasta R., Moglia C., Calvo A., Origone P., Chio A., Mandich P.

    المساهمون: Lanteri P., Meola I., Canosa A., De Marco G., Lomartire A., Rinaudo M.T., Albamonte E., Sansone V.A., Lunetta C., Manera U., Vasta R., Moglia C., Calvo A., Origone P., Chio A., Mandich P.

    مصطلحات موضوعية: FUS gene, Juvenile amyotrophic lateral sclerosi, Truncated FUS protein expression

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33637330; info:eu-repo/semantics/altIdentifier/wos/MEDLINE:33637330; firstpage:1; lastpage:4; numberofpages:4; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2318/1778138Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85101375527

    الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2021.01.029Test
    http://hdl.handle.net/2318/1778138Test

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  2. 2
    The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment

    المؤلفون: Irene Meola, Maria Teresa Rinaudo, Giovanni de Marco, Christian Lunetta, Paola Origone, Emilio Albamonte, Adriano Chiò, Cristina Moglia, Paola Mandich, Valeria A. Sansone, Annarosa Lomartire, Rosario Vasta, Antonio Canosa, Andrea Calvo, Umberto Manera, Paola Lanteri

    مصطلحات موضوعية: 0301 basic medicine, Proband, Aging, medicine.medical_specialty, Heterozygote, Juvenile amyotrophic lateral sclerosis, Gene Expression, Loss of Heterozygosity, Gene mutation, medicine.disease_cause, FUS gene, 03 medical and health sciences, Exon, 0302 clinical medicine, Internal medicine, medicine, Humans, Cognitive Dysfunction, RNA, Messenger, Truncated FUS protein expression, Child, Genetic Association Studies, Mutation, biology, business.industry, General Neuroscience, Amyotrophic Lateral Sclerosis, Wild type, Exons, 030104 developmental biology, Endocrinology, biology.protein, Disease Progression, RNA-Binding Protein FUS, Female, Neurology (clinical), Geriatrics and Gerontology, Antibody, business, 030217 neurology & neurosurgery, Nuclear localization sequence, Developmental Biology

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10c9399758a8ee88ea463149dac02123Test
    http://hdl.handle.net/2318/1778138Test


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