Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Johanna Kaindl"'
Autor:
Laura Krumm, Tatyana Pozner, Johanna Kaindl, Martin Regensburger, Claudia Günther, Soeren Turan, Reza Asadollahi, Anita Rauch, Beate Winner
Publikováno v:
Stem Cell Research, Vol 56, Iss , Pp 102520- (2021)
Pathogenic bi-allelic variants in the SPG11 gene result in rare motor neuron disorders such as Hereditary Spastic Paraplegia type 11, Charcot-Marie Tooth, and Juvenile Amyotrophic Lateral Sclerosis-5. The main challenge in SPG11-linked disease resear
Externí odkaz:
https://doaj.org/article/1e3dd390cc214c3c924d5363a917a04f
Autor:
Jonas Lanfer, Johanna Kaindl, Laura Krumm, Miguel Gonzalez Acera, Markus Neurath, Martin Regensburger, Florian Krach, Beate Winner
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 9, p 4526 (2022)
Current protocols converting human induced pluripotent stem cells (iPSCs) into induced microglia-like cells (iMGL) are either dependent on overexpression of transcription factors or require substantial experience in stem-cell technologies. Here, we d
Externí odkaz:
https://doaj.org/article/0ed85ed52bdf4f859c8a7ab73b7d8cb5
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2020)
Parkinson’s disease (PD) is the most frequently occurring movement disorder, with an increasing incidence due to an aging population. For many years, the post-mortem brain was regarded as the gold standard for the analysis of the human pathology of
Externí odkaz:
https://doaj.org/article/633ec386d4e04474bceaff1c6b569ad2
Autor:
Claudia Günther, Laura Krumm, Martin Regensburger, Reza Asadollahi, Johanna Kaindl, Beate Winner, Soeren Turan, Anita Rauch, Tatyana Pozner
Publikováno v:
Stem Cell Research, Vol 56, Iss, Pp 102520-(2021)
Pathogenic bi-allelic variants in the SPG11 gene result in rare motor neuron disorders such as Hereditary Spastic Paraplegia type 11, Charcot-Marie Tooth, and Juvenile Amyotrophic Lateral Sclerosis-5. The main challenge in SPG11-linked disease resear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8457c1543718bb79c561f4a9acaa8a42
https://pubmed.ncbi.nlm.nih.gov/34479069
https://pubmed.ncbi.nlm.nih.gov/34479069
Autor:
Heiko Zimmermann, Julia Majer, Johanna Kaindl, Ina Meiser, Florian Krach, Jürgen Winkler, Alisa Katsen-Globa, Julia C. Neubauer, Beate Winner, Annika Sommer
Publikováno v:
Stem Cells Translational Medicine
Human induced pluripotent stem cells (hiPSCs) are an important tool for research and regenerative medicine, but their efficient cryopreservation remains a major challenge. The current gold standard is slow-rate freezing of dissociated colonies in sus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00b6c80f3beeed626cf0174d1147723
https://doi.org/10.1002/sctm.18-0121
https://doi.org/10.1002/sctm.18-0121
Autor:
Johanna, Kaindl, Beate, Winner
Publikováno v:
Current topics in behavioral neurosciences. 42
Human pluripotent stem (PS) cells are a relevant platform to model human-specific neurological disorders. In this chapter, we focus on human stem cell models for neuropsychiatric disorders including induced pluripotent stem (iPS) cell-derived neural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98755e15ae001fa916600a61d142f99c
https://pubmed.ncbi.nlm.nih.gov/31407242
https://pubmed.ncbi.nlm.nih.gov/31407242
Autor:
Beate Winner, Johanna Kaindl
Publikováno v:
Behavioral Neurogenomics ISBN: 9783030312640
Human pluripotent stem (PS) cells are a relevant platform to model human-specific neurological disorders. In this chapter, we focus on human stem cell models for neuropsychiatric disorders including induced pluripotent stem (iPS) cell-derived neural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65de5337949ec9eb95b967526f8b3bef
https://doi.org/10.1007/7854_2019_111
https://doi.org/10.1007/7854_2019_111
Autor:
Lanfer, Jonas1 (AUTHOR) jonas.lanfer@fau.de, Kaindl, Johanna1 (AUTHOR) johanna.kaindl@alumni.fau.de, Krumm, Laura1 (AUTHOR) laura.krumm@uk-erlangen.de, Gonzalez Acera, Miguel2 (AUTHOR) miguel.gonzalezacera@uk-erlangen.de, Neurath, Markus2,3 (AUTHOR) markus.neurath@uk-erlangen.de, Regensburger, Martin1,4,5 (AUTHOR) martin.regensburger@uk-erlangen.de, Krach, Florian1 (AUTHOR) flo.krach@fau.de, Winner, Beate1,3,4 (AUTHOR) beate.winner@fau.de
Publikováno v:
International Journal of Molecular Sciences. May2022, Vol. 23 Issue 9, p4526-4526. 12p.
Autor:
Prieto Huarcaya, Susy, Drobny, Alice, Marques, André R. A., Di Spiezio, Alessandro, Dobert, Jan Philipp, Balta, Denise, Werner, Christian, Rizo, Tania, Gallwitz, Lisa, Bub, Simon, Stojkovska, Iva, Belur, Nandkishore R., Fogh, Jens, Mazzulli, Joseph R, Xiang, Wei, Fulzele, Amitkumar, Dejung, Mario, Sauer, Markus, Winner, Beate, Rose-John, Stefan
Publikováno v:
Autophagy; May2022, Vol. 18 Issue 5, p1127-1151, 25p
Publikováno v:
Frontiers in Cellular Neuroscience; 1/17/2020, Vol. 13, p1-14, 14p