Bettina Schmid - Publications

Affiliations: 
LMU - Munich 

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Hipke K, Pitter B, Hruscha A, van Bebber F, Modic M, Bansal V, Lewandowski SA, Orozco D, Edbauer D, Bonn S, Haass C, Pohl U, Montanez E, Schmid B. Loss of TDP-43 causes ectopic endothelial sprouting and migration defects through increased , and . Frontiers in Cell and Developmental Biology. 11: 1169962. PMID 37384248 DOI: 10.3389/fcell.2023.1169962  0.323
2020 Oberhofer A, Reithmann E, Spieler P, Stepp WL, Zimmermann D, Schmid B, Frey E, Ökten Z. Molecular underpinnings of cytoskeletal cross-talk. Proceedings of the National Academy of Sciences of the United States of America. PMID 32041870 DOI: 10.1073/Pnas.1917964117  0.306
2019 Espin Palazon R, Cheng X, Campbell CA, Li L, Schmid B, Traver D. Zebra "Fishing" the Role of Granulin in Hematopoiesis Blood. 134: 1194-1194. DOI: 10.1182/Blood-2019-130781  0.337
2015 Solchenberger B, Russell C, Kremmer E, Haass C, Schmid B. Granulin knock out zebrafish lack frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis pathology. Plos One. 10: e0118956. PMID 25785851 DOI: 10.1371/Journal.Pone.0118956  0.347
2013 Haass C, van Bebber F, Hruscha A, Willem M, Schmid B. O1-08-05: Distinct functions of BACE1 and BACE2 in neuregulin processing and melanocyte migration Alzheimer's & Dementia. 9: P144-P144. DOI: 10.1016/J.Jalz.2013.04.096  0.331
2008 Dooley KA, Fraenkel PG, Langer NB, Schmid B, Davidson AJ, Weber G, Chiang K, Foott H, Dwyer C, Wingert RA, Zhou Y, Paw BH, Zon LI. montalcino, A zebrafish model for variegate porphyria. Experimental Hematology. 36: 1132-42. PMID 18550261 DOI: 10.1016/J.Exphem.2008.04.008  0.368
2008 Shankaran SS, Capell A, Hruscha AT, Fellerer K, Neumann M, Schmid B, Haass C. Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. The Journal of Biological Chemistry. 283: 1744-53. PMID 17984093 DOI: 10.1074/Jbc.M705115200  0.314
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