Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Cilium assembly"'
Autor:
Sarra E. Jamieson, Richard W. Francis, Timo Lassmann, Elizabeth S. H. Scaman, Jenefer M. Blackwell, Heather J. Cordell, Dave Tang, Genevieve Syn, Harvey Coates, Michaela Fakiola, Denise Anderson
Publikováno v:
Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
Background Our goal was to identify genetic risk factors for severe otitis media (OM) in Aboriginal Australians. Methods Illumina® Omni2.5 BeadChip and imputed data were compared between 21 children with severe OM (multiple episodes chronic suppurat
Publikováno v:
Journal of Cellular Physiology
The primary cilium is an antennae‐like structure extent outside the cell surface. It has an important role in regulating cell‐signaling transduction to affect proliferation, differentiation and migration. Evidence is accumulating that ciliary def
Akademický článek
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Akademický článek
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Autor:
Zbynek Zdrahal, David Vyslouzil, Ondrej Bernatik, Katerina Hanakova, Petra Pejskova, Lukas Cajanek
Publikováno v:
Molecular Biology of the Cell
Primary cilia (PC) are organelles necessary for proper implementation of developmental and homeostasis processes. To initiate their assembly, coordinated actions of multiple proteins are needed. Tau tubulin kinase 2 (TTBK2) is a key player in the cil
Autor:
Ewelina Bukowska-Olech, Aleksander Jamsheer, Machteld M. Oud, Anna Wasilewska, Heleen H. Arts, Anna Wawrocka, Anna Latos-Bielenska, Joanna Walczak-Sztulpa, Renata Posmyk, Miriam Schmidts
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Orphanet Journal of Rare Diseases, 15
Orphanet Journal of Rare Diseases, 15, 1
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 15
Orphanet Journal of Rare Diseases, 15, 1
Orphanet Journal of Rare Diseases
Background Sensenbrenner syndrome, which is also known as cranioectodermal dysplasia (CED), is a rare, autosomal recessive ciliary chondrodysplasia characterized by a variety of clinical features including a distinctive craniofacial appearance as wel
Autor:
Robert Sullivan, Christine Légaré
Publikováno v:
Andrology. 8:625-636
BACKGROUND Gene expression patterns along the epididymis are established by specific transcription factor networks that coordinate region-specific functions. In rodents, the epididymis can be divided in up to 19 segments. Based on gross anatomy, the
Autor:
Sergi Rodriguez-Calado, Petra Van Damme, Francesc Xavier Avilés, Ana Paula Candiota, Sebastian Tanco, Julia Lorenzo
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 2; Pages: 1273
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
The cytosolic carboxypeptidase 6 (CCP6) catalyzes the deglutamylation of polyglutamate side chains, a post-translational modification that affects proteins such as tubulins or nucleosome assembly proteins. CCP6 is involved in several cell processes,
Autor:
Qing-Bo Lv, Yang-Yuan Qiu, Chun-Ren Wang, Yun-Yi Sun, Rui-Feng Mao, Qiao-Cheng Chang, Ying-Yu Chen, Jun-Feng Gao
Publikováno v:
Frontiers in Cellular and Infection Microbiology
Frontiers in Cellular and Infection Microbiology, Vol 11 (2021)
Frontiers in Cellular and Infection Microbiology, Vol 11 (2021)
Metorchis orientalis is a neglected zoonotic parasite of the gallbladder and bile duct of poultry, mammals, and humans. It has been widely reported in Asian, including China, Japanese, and Korea, where it is a potential threat to public health. Despi
Autor:
SM Niedziółka, S Datta, T Uśpieński, B Baran, W Skarżyńska, EW Humke, R Rohatgi, P Niewiadomski
The efficient transport of proteins into the primary cilium is a crucial step for many signaling pathways. Dysfunction of this process can lead to the disruption of signaling cascades or cilium assembly, resulting in developmental disorders and cance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::774565ef2a6925e720b1e83cf1cbf33e
https://doi.org/10.1101/2021.09.27.461918
https://doi.org/10.1101/2021.09.27.461918