Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fabio Marsoner"'
Autor:
Vira Iefremova, George Manikakis, Olivia Krefft, Ammar Jabali, Kevin Weynans, Ruven Wilkens, Fabio Marsoner, Björn Brändl, Franz-Josef Müller, Philipp Koch, Julia Ladewig
Publikováno v:
Cell Reports, Vol 19, Iss 1, Pp 50-59 (2017)
Miller-Dieker syndrome (MDS) is caused by a heterozygous deletion of chromosome 17p13.3 involving the genes LIS1 and YWHAE (coding for 14.3.3ε) and leads to malformations during cortical development. Here, we used patient-specific forebrain-type org
Externí odkaz:
https://doaj.org/article/c701dea2353743df96edf83284792c53
Autor:
Andrea Carlo Rossetti, Olivia Fechtner, Camille Maillard, Anne Hoffrichter, Lea Zillich, Eric Poisel, Ammar Jabali, Fabio Marsoner, Ruven Wilkens, Fiona Francis, Nadia Bahi-Buisson, Philipp Koch, Julia Ladewig
Lissencephaly is a developmental cortical malformation characterized by reduced to absent gyri and a disorganized cortex. Heterozygous mutations in the LIS1 gene, encoding a regulator of the microtubule-motor dynein, were identified to cause lissence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a93b9c89e788a50b4d76a699e3fc9e7
https://doi.org/10.1101/2022.12.19.520907
https://doi.org/10.1101/2022.12.19.520907
Autor:
Jan, Fischer, Eduardo Fernández, Ortuño, Fabio, Marsoner, Annasara, Artioli, Jula, Peters, Takashi, Namba, Christina Eugster, Oegema, Wieland B, Huttner, Julia, Ladewig, Michael, Heide
Publikováno v:
EMBO reports. 23(11)
The human-specific gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::28e94e815683083ccf9e3398e02bf637
https://pubmed.ncbi.nlm.nih.gov/36161459
https://pubmed.ncbi.nlm.nih.gov/36161459
Autor:
Jan Fischer, Eduardo Fernández Ortuño, Fabio Marsoner, Annasara Artioli, Jula Peters, Takashi Namba, Christina Eugster Oegema, Wieland B. Huttner, Julia Ladewig, Michael Heide
Publikováno v:
EMBO reports. 23
The human-specific gene ARHGAP11B has been implicated in human neocortex expansion. However, the extent of ARHGAP11B's contribution to this expansion during hominid evolution is unknown. Here we address this issue by genetic manipulation of ARHGAP11B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a8d0cb31df3e618bdc0cb5038d6c88
https://doi.org/10.15252/embr.202254728
https://doi.org/10.15252/embr.202254728
Autor:
Ammar Jabali, Anne Hoffrichter, Ana Uzquiano, Fabio Marsoner, Ruven Wilkens, Marco Siekmann, Bettina Bohl, Andrea C Rossetti, Sandra Horschitz, Philipp Koch, Fiona Francis, Julia Ladewig
Publikováno v:
EMBO Reports
EMBO Reports, 2022, 23 (5), ⟨10.15252/embr.202154027⟩
EMBO Reports, 2022, 23, ⟨10.15252/embr.202154027⟩
EMBO Reports, 2022, 23 (5), ⟨10.15252/embr.202154027⟩
EMBO Reports, 2022, 23, ⟨10.15252/embr.202154027⟩
International audience; Malformations of human cortical development (MCD) can cause severe disabilities. The lack of human-specific models hampers our understanding of the molecular underpinnings of the intricate processes leading to MCD. Here, we us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca3ee6ac1e4640d35b90e245df0fb603
https://hal.sorbonne-universite.fr/hal-03744114
https://hal.sorbonne-universite.fr/hal-03744114
Autor:
Jacopo Zasso, Matteo Marcatili, Fabio Marsoner, Luigi A. Lanterna, Thodoris Karnavas, Marina Cardano, Luciano Conti
Publikováno v:
Stem Cell Research. 17:623-626
Peripheral blood mononuclear cells (PBMCs) were collected from 55-year old male patient with a confirmed diagnosis of hemorrhagic Moyamoya disease (MMD). PBMCs were reprogrammed using Sendai virus particles delivering the four Yamanaka factors. A foo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f5a3fa1206b0cb57467b68a5971a29
https://doi.org/10.1016/j.scr.2016.11.006
https://doi.org/10.1016/j.scr.2016.11.006
Autor:
Matteo Marcatili, Armando D'Agostino, Silvio Scarone, Luciano Conti, Fabio Marsoner, Thodoris Karnavas, Daniele Bottai
Publikováno v:
Stem Cell Research. 17:630-633
Peripheral blood mononuclear cells (PBMCs) were collected from a patient with treatment-refractory Schizophrenia who presented an exceptional clinical response to Clozapine. iPSC lines were established with a non-integrating reprogramming system base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb23dbbbf5ad0b2513519940a8cebb6c
https://doi.org/10.1016/j.scr.2016.11.009
https://doi.org/10.1016/j.scr.2016.11.009
Publikováno v:
Current opinion in geneticsdevelopment. 52
The development of organoids derived from human pluripotent stem cells heralded a new area in studying human organ development and pathology outside of the human body. Triggered by the seminal work of pioneers in the field such as Yoshiki Sasai or Ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ddf65db7ce8f328fcc13dadad88153a
https://pubmed.ncbi.nlm.nih.gov/29807351
https://pubmed.ncbi.nlm.nih.gov/29807351
Autor:
Vira Iefremova, Franz-Josef Müller, Ammar Jabali, Julia Ladewig, Ruven Wilkens, Fabio Marsoner, George Manikakis, Olivia Krefft, Philipp Koch, Björn Brändl, Kevin Weynans
Publikováno v:
Cell Reports, Vol 19, Iss 1, Pp 50-59 (2017)
Miller-Dieker syndrome (MDS) is caused by a heterozygous deletion of chromosome 17p13.3 involving the genes LIS1 and YWHAE (coding for 14.3.3ε) and leads to malformations during cortical development. Here, we used patient-specific forebrain-type org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3649ab8623cca8f734705e0bdf58fd
https://pubmed.ncbi.nlm.nih.gov/28380362
https://pubmed.ncbi.nlm.nih.gov/28380362
Autor:
Fabio Marsoner, Jacopo Zasso, Luciano Conti, Matteo Marcatili, Marina Cardano, Thodoris Karnavas, Luigi A. Lanterna
Peripheral blood mononuclear cells (PBMCs) were collected from an 8-year old female patient affected by ischemic Moyamoya disease (MMD). Patient's PBMCs were reprogrammed using Sendai virus particles delivering the four Yamanaka factors. The footprin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4355746ca83f8563fc335bd337e2cd73
http://hdl.handle.net/11572/174788
http://hdl.handle.net/11572/174788