Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Allen D. Seol"'
Autor:
Jon F. Robinson, Thomas R. Noriega, Christopher L. Bennett, Kevin C. Corbit, María Salomé Sirerol-Piquer, Dragana Josifova, Friedhelm Hildebrandt, Edgar A. Otto, Allen D. Seol, Francesc R. Garcia-Gonzalo, Jeremy F. Reiter, José Manuel García-Verdugo, Gokul Ramaswami, Nicholas Katsanis
Publikováno v:
Nature genetics
NATURE GENETICS
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
Nature genetics, vol 43, iss 8
NATURE GENETICS
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
Nature genetics, vol 43, iss 8
Mutations in genes encoding ciliary components cause ciliopathies, but how many of these mutations disrupt ciliary function is unclear. We investigated Tectonic1 (Tctn1), a regulator of mouse Hedgehog signaling, and found that it is essential for cil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f419f22f4131d56265957b8d118aeacb
http://europepmc.org/articles/PMC3145011
http://europepmc.org/articles/PMC3145011
Autor:
Friedhelm Hildebrandt, Suzie J. Scales, Heiko Reutter, Matthew J. Brauer, Muhammad Rafiq, Abdul Noor, Edgar A. Otto, Wendy Sandoval, Julie J. Miller, Priya Kulkarni, Mindan K. Sfakianos, John B. Vincent, Val C. Sheffield, Xiaohui Wen, Susanne Held, Dan Doherty, J. Fernando Bazan, Allen D. Seol, Liyun Sang, Akella Radha Rama Devi, William S. Lane, Mandy Kwong, Diane C. Slusarski, Muhammad Ansar, Francesc R. Garcia-Gonzalo, Jeremy F. Reiter, Peter K. Jackson, Erik Huntzicker, Lisa M. Baye, John F. O'Toole, Kevin C. Corbit, Rachel H. Giles
Publikováno v:
Cell; Vol 145
SummaryNephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are autosomal-recessive ciliopathies presenting with cystic kidneys, retinal degeneration, and cerebellar/neural tube malformation. Whether defects in kidney, retinal,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53c1cf88093f823a4a6d0db2deedce5c
Autor:
Veena Singla, Julie Hunkapiller, Paul Wakenight, William C. Skarnes, Nicole Santos, Allen D. Seol, Jeremy F. Reiter, Andrew R. Norman
Publikováno v:
Nature Methods. 7:50-52
We describe a method for the highly efficient and precise targeted modification of gene trap loci in mouse embryonic stem cells (ESCs). Through the Floxin method, gene trap mutations were reverted and new DNA sequences inserted using Cre recombinase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01226add9e8f10a9a34f1f637d4bd669
https://doi.org/10.1038/nmeth.1406
https://doi.org/10.1038/nmeth.1406
Autor:
María Salomé Sirerol-Piquer, Allen D. Seol, Andrew Kodani, Jeremy F. Reiter, José Manuel García-Verdugo
Publikováno v:
The EMBO journal, vol 32, iss 4
EMBO JOURNAL
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
EMBO JOURNAL
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
Formation of cilia, microtubule-based structures that function in propulsion and sensation, requires Kif3a, a subunit of Kinesin II essential for intraflagellar transport (IFT). We have found that, Kif3a is also required to organize centrioles. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e01d04f5c96b01d13533180e4ef216a5
https://escholarship.org/uc/item/0pv3q3jp
https://escholarship.org/uc/item/0pv3q3jp
Oral-Facial-Digital 1 (OFD1) Syndrome is an X-linked developmental disorder caused by mutations in the gene Ofd1. OFD1 syndrome involves malformation of the face, oral cavity, and digits and may be characterized by cystic kidneys and mental retardati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a18aa8097bf8b5cacf439178182807c9
https://europepmc.org/articles/PMC3128778/
https://europepmc.org/articles/PMC3128778/
Autor:
Christopher K. Bichakjian, Allen D. Seol, Alexandre N. Ermilov, Ervin H. Epstein, Jeremy F. Reiter, Po-Lin So, Sunny Y. Wong, Andrzej A. Dlugosz
Primary cilia are present on most mammalian cells and are implicated in transducing Hedgehog (Hh) signals during development; however, the prevalence of cilia on human tumors remains unclear, and the role of cilia in cancer has not been examined. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9a0f7f3c15c5276cc46a3e9991f762
https://europepmc.org/articles/PMC2895420/
https://europepmc.org/articles/PMC2895420/
Publikováno v:
International Journal of Developmental Neuroscience. 28:644-644
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac7e7490079aa1a8b02a410276e0c11
https://doi.org/10.1016/j.ijdevneu.2010.07.014
https://doi.org/10.1016/j.ijdevneu.2010.07.014