Zobrazeno 1 - 10
of 26
pro vyhledávání: '"lim-homeodomain protein"'
Autor:
Satoru Shinkuma, Hideki Nakamura, Manami Maehara, Shota Takashima, Toshifumi Nomura, Yasuyuki Fujita, Satoshi Hasegawa, Kazuko C. Sato-Matsumura, Riichiro Abe, Hiroshi Shimizu
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1110-1115 (2019)
Nail-patella syndrome is an autosomal dominant disorder characterized by nail dysplasia and skeletal anomaly. Some patients have been shown to have ultrastructural abnormalities of the glomerular basement membrane that result in nephrosis. However, l
Externí odkaz:
https://doaj.org/article/fb06c7581dd3427a82c2b1e6c375d5af
Autor:
Pulcrano, Salvatore, De Gregorio, Roberto, De Sanctis, Claudia, Lahti, Laura, Perrone-Capano, Carla, Ponti, Donatella, Di Porzio, Umberto, Perlmann, Thomas, Caiazzo, Massimiliano, Volpicelli, Floriana, Bellenchi, Gian Carlo, Afd Pharmaceutics, Pharmaceutics
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 13; Pages: 6961
International Journal of Molecular Sciences, 23(13), 1. MDPI AG
International Journal of Molecular Sciences, 23(13), 1. MDPI AG
The development of midbrain dopaminergic (DA) neurons requires a fine temporal and spatial regulation of a very specific gene expression program. Here, we report that during mouse brain development, the microRNA (miR-) 204/211 is present at a high le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eccee8cccf89e0f24732024a3459debc
Autor:
Hideki Nakamura, Kazuko C. Sato-Matsumura, Shota Takashima, Yasuyuki Fujita, Toshifumi Nomura, Manami Maehara, Hiroshi Shimizu, Satoru Shinkuma, Riichiro Abe, Hasegawa Satoshi
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1110-1115 (2019)
Nail-patella syndrome is an autosomal dominant disorder characterized by nail dysplasia and skeletal anomaly. Some patients have been shown to have ultrastructural abnormalities of the glomerular basement membrane that result in nephrosis. However, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379f33288e0e0d2c48044f05781cc285
https://pubmed.ncbi.nlm.nih.gov/31513274
https://pubmed.ncbi.nlm.nih.gov/31513274
Autor:
Abdul K. Sesay, Grant Roalfe, Guilherme Neves, Petros Liodis, Matthew C. Walker, Vassilis Pachnis, Angeliki Achimastou, Mala M. Shah, Myrto Denaxa
Publikováno v:
Cerebral Cortex (New York, NY)
Deletion of LIM homeodomain transcription factor-encoding Lhx6 gene in mice results in defective tangential migration of cortical interneurons and failure of differentiation of the somatostatin (Sst)- and parvalbumin (Pva)-expressing subtypes. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eff8d82706a743a0f9cbbade0686fa9
https://doi.org/10.1093/cercor/bhs159
https://doi.org/10.1093/cercor/bhs159
Autor:
Tatyana D. Sotnikova, Giorgia Colciago, Vania Broccoli, Giovanni Russo, Stefano Gustincich, Andrea Menegon, Massimiliano Caiazzo, Dejan Lazarevic, Alexander Dityatev, Raul R. Gainetdinov, Maria Teresa Dell’Anno, Paola Roncaglia, Elena Dvoretskova, Piero Carninci, Stefano Taverna, Gianni Pezzoli, Damiana Leo
Publikováno v:
Nature; Vol 476
Nature
Nature
Transplantation of dopaminergic neurons can potentially improve the clinical outcome of Parkinson's disease, a neurological disorder resulting from degeneration of mesencephalic dopaminergic neurons. In particular, transplantation of embryonic-stem-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::621e318b8d71b7cc44180bb6f7d6ec7c
Autor:
Naoko Taniguchi-Ishigaki, Catherina G. Becker, Lalitha Nagarajan, Zhen Zhong, Thomas Becker, Hong Ma, Ingolf Bach
Publikováno v:
Zhong, Z, Ma, H, Taniguchi-Ishigaki, N, Nagarajan, L, Becker, C G, Bach, I & Becker, T 2011, ' SSDP cofactors regulate neural patterning and differentiation of specific axonal projections ', Developmental Biology, vol. 349, no. 2, pp. 213-24 . https://doi.org/10.1016/j.ydbio.2010.10.037
The developmental activity of LIM homeodomain transcription factors (LIM-HDs) is critically controlled by LIM domain-interacting cofactors of LIM-HDs (CLIM, also known as NLI or LDB). CLIM cofactors associate with single-stranded DNA binding proteins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1d592687c85d9442f7bf26b52139e5b
Publikováno v:
Developmental Biology. 244(2):278-292
The generation of distinct classes of motor neurons underlies the development of complex motile behavior in all animals and is well characterized in chordates. Recent molecular studies indicate that the ascidian larval central nervous system (CNS) ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e763c40722c95be8be5545a8c555148a
Autor:
Damiana Leo, Alexander Dityatev, Raul R. Gainetdinov, Federica Ungaro, Maria Teresa Dell’Anno, Vania Broccoli, Francesca Managò, Massimiliano Caiazzo, Ilda Theka, Gianni Pezzoli, Sebastiano Curreli, Elena Dvoretskova
Current protocols for in vitro differentiation of human induced pluripotent stem cells (hiPSCs) to generate dopamine (DA) neurons are laborious and time-expensive. In order to accelerate the overall process, we have established a fast protocol by exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a13ed14b527507d459073334d2aa36a1
http://hdl.handle.net/11567/799248
http://hdl.handle.net/11567/799248
Autor:
Laura Spinardi, Edoardo Migliori, Luca G. Guidotti, Elisa Lenti, Richard P. Harvey, Sara Maruzzelli, Diego Farinello, Zachary Harrelson, Andrea Brendolan, Laura Castagnaro, Sylvia M. Evans, Giovanni Sitia
Publikováno v:
Immunity
Secondary lymphoid organ stromal cells comprise different subsets whose origins remain unknown. Herein, we exploit a genetic lineage-tracing approach to show that splenic fibroblastic reticular cells (FRCs), follicular dendritic cells (FDCs), margina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9fff82a8b0985869160a67b9eae7b50
https://pubmed.ncbi.nlm.nih.gov/23642357
https://pubmed.ncbi.nlm.nih.gov/23642357
Autor:
Ramon Brugada, James T. Willerson, Achim Bell, Tack Ki Leung, Robert J. Schwartz, Raffaella Lombardi, Jinjiang Dong, Ali J. Marian, Gabriela Rodriguez
The phenotypic hallmark of arrhythmogenic right ventricular cardiomyopathy, a genetic disease of desmosomal proteins, is fibroadipocytic replacement of the right ventricle. Cellular origin of excess adipocytes, the responsible mechanism(s) and the ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5167cbb28944d6fcb4dae8294a34ac
http://hdl.handle.net/11588/790666
http://hdl.handle.net/11588/790666