Výsledky vyhledávání - "Bruna Baumgarten Krebs"

Akademický článek

Amyotrophic Lateral Sclerosis Type 20 - In Silico Analysis and Molecular Dynamics Simulation of hnRNPA1.

Autor: Bruna Baumgarten Krebs, Joelma Freire De Mesquita

Publikováno v: PLoS ONE, Vol 11, Iss 7, p e0158939 (2016)

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease that affects the upper and lower motor neurons. 5-10% of cases are genetically inherited, including ALS type 20, which is caused by mutations in the hnRNPA1 gene. The goals of t

Externí odkaz: https://doaj.org/article/063de119a2a14f3ca5d6b2b62e97d50a

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Enhanced FGFR3 activity in postmitotic principal neurons during brain development results in cortical dysplasia and axonal tract abnormality

Autor: Jui-Yen Huang, Hui-Chen Lu, Jason Michael Graf, May Lin Russell, Bruna Baumgarten Krebs, Marisha Lynn Miskus, Eamonn Patrick Duffy

Publikováno v: Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-20 (2020)

Abnormal levels of fibroblast growth factors (FGFs) and FGF receptors (FGFRs) have been detected in various neurological disorders. The potent impact of FGF-FGFR in multiple embryonic developmental processes makes it challenging to elucidate their ro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfa027abaeb22c88bee1b94728601865
http://europepmc.org/articles/PMC7595096

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Enhanced FGFR3 activity in post-mitotic principal neurons during brain development results in cortical dysplasia and axon miswiring

Autor: Eamonn Patrick Duffy, Jui-Yen Huang, May Lin Russell, Marisha Lynn Miskus, Hui-Chen Lu, Bruna Baumgarten Krebs, Jason Michael Graf

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::582009ecc2c706405f768e8934e3640b

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Amyotrophic Lateral Sclerosis Type 20 - In Silico Analysis and Molecular Dynamics Simulation of hnRNPA1

Autor: Joelma Freire De Mesquita, Bruna Baumgarten Krebs

Publikováno v: PLoS ONE
PLoS ONE, Vol 11, Iss 7, p e0158939 (2016)

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease that affects the upper and lower motor neurons. 5–10% of cases are genetically inherited, including ALS type 20, which is caused by mutations in the hnRNPA1 gene. The goals of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b93ab3c0932c839d96f18197a29649d
https://pubmed.ncbi.nlm.nih.gov/27414033

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