Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Michael J Dixon"'
Autor:
Michael D Rotelli, Robert A Policastro, Anna M Bolling, Andrew W Killion, Abraham J Weinberg, Michael J Dixon, Gabriel E Zentner, Claire E Walczak, Mary A Lilly, Brian R Calvi
Publikováno v:
PLoS Genetics, Vol 15, Iss 7, p e1008253 (2019)
Endoreplication is a cell cycle variant that entails cell growth and periodic genome duplication without cell division, and results in large, polyploid cells. Cells switch from mitotic cycles to endoreplication cycles during development, and also in
Externí odkaz:
https://doaj.org/article/9b03fb4650ca4d9a83cd8d323520dde5
Autor:
Rose Richardson, Karen Mitchell, Nigel L Hammond, Maria Rosaria Mollo, Evelyn N Kouwenhoven, Niki D Wyatt, Ian J Donaldson, Leo Zeef, Tim Burgis, Rognvald Blance, Simon J van Heeringen, Hendrik G Stunnenberg, Huiqing Zhou, Caterina Missero, Rose Anne Romano, Satrajit Sinha, Michael J Dixon, Jill Dixon
Publikováno v:
PLoS Genetics, Vol 13, Iss 6, p e1006828 (2017)
Cleft palate is a common congenital disorder that affects up to 1 in 2500 live births and results in considerable morbidity to affected individuals and their families. The aetiology of cleft palate is complex with both genetic and environmental facto
Externí odkaz:
https://doaj.org/article/b209f22d14c644fb950be3f75503ac4f
Publikováno v:
Frontiers in Psychology, Vol 4 (2013)
Time-space synaesthetes ‘see’ time units organized in a spatial form. While the structure might be invariant for most synaesthetes, the perspective by which some view their calendar is somewhat flexible. One well-studied synaesthete L adopts diff
Externí odkaz:
https://doaj.org/article/d63872bd9e3f49478031930665d5d5c6
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59533 (2013)
In human, mutation of the transcription factor SATB2 causes severe defects to the palate and jaw. The expression and sequence of SATB2 is highly conserved across vertebrate species, including zebrafish. We sought to understand the regulation of satb2
Externí odkaz:
https://doaj.org/article/79781621334240cabfda61f1a67a5a82
Publikováno v:
PLoS Genetics, Vol 8, Iss 3, p e1002566 (2012)
The cerebral cortex is a specialized region of the brain that processes cognitive, motor, somatosensory, auditory, and visual functions. Its characteristic architecture and size is dependent upon the number of neurons generated during embryogenesis a
Externí odkaz:
https://doaj.org/article/489b480403394a619c6dcde58739b7c7
Autor:
Ulrike Romatschke, Michael J. Dixon
Publikováno v:
Journal of Atmospheric and Oceanic Technology. 39:1705-1716
Using data from the airborne HIAPER Cloud Radar (HCR), a partitioning algorithm (ECCO-V) that provides vertically resolved convectivity and convective versus stratiform radar-echo classification is developed for vertically pointing radars. The algori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e58230e2c95349c1227791d75ad7a4b8
https://doi.org/10.1175/jtech-d-22-0019.1
https://doi.org/10.1175/jtech-d-22-0019.1
Autor:
Nigel L. Hammond, Michael J. Dixon
Publikováno v:
Oral Diseases. 28:1306-1326
Clefts of the lip and palate (CLP), the major causes of congenital facial malformation globally, result from failure of fusion of the facial processes during embryogenesis. With a prevalence of 1 in 500-2500 live births, CLP causes major morbidity th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01dcb745317f699925edcfb7d3b83a6f
https://doi.org/10.1111/odi.14174
https://doi.org/10.1111/odi.14174
Autor:
Karla T. Falcon, Kristin E. N. Watt, Soma Dash, Ruonan Zhao, Daisuke Sakai, Emma L. Moore, Sharien Fitriasari, Melissa Childers, Mihaela E. Sardiu, Selene Swanson, Dai Tsuchiya, Jay Unruh, George Bugarinovic, Lin Li, Rita Shiang, Annita Achilleos, Jill Dixon, Michael J. Dixon, Paul A. Trainor
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 119(31)
Ribosomal RNA (rRNA) transcription by RNA polymerase I (Pol I) is a critical rate-limiting step in ribosome biogenesis, which is essential for cell survival. Despite its global function, disruptions in ribosome biogenesis cause tissue-specific birth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::425cce96ef112a1030fe15af2b7b08f1
https://pubmed.ncbi.nlm.nih.gov/35881792
https://pubmed.ncbi.nlm.nih.gov/35881792
Autor:
Tatyana D, Kolesnikova, Mikhail S, Klenov, Alina R, Nokhova, Sergey A, Lavrov, Galina V, Pokholkova, Veit, Schubert, Svetlana V, Maltseva, Kevin R, Cook, Michael J, Dixon, Igor F, Zhimulev
Publikováno v:
Cells. 11(23)
The pericentromeric heterochromatin is largely composed of repetitive sequences, making it difficult to analyze with standard molecular biological methods. At the same time, it carries many functional elements with poorly understood mechanisms of act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9b58b6ab4fd5034c23d6902c98e163d
https://pubmed.ncbi.nlm.nih.gov/36497131
https://pubmed.ncbi.nlm.nih.gov/36497131
Autor:
Bert Braumann, Khalid Aldhorae, Carlo Maj, Elisabeth Mangold, Kerstin U. Ludwig, Peter Krawitz, Alexander Hoischen, Andreas Jäger, Frederic Thieme, Nigel L. Hammond, Christian Gilissen, Michael J. Dixon, Angelika Biedermann, John Bowes, Hanna K. Zieger, Jonas Hausen, Antony Adamson, Leonie Henschel, Andreas Buness, Thomas Kreusch, Teresa Kruse, Nina Ishorst, Lina Gölz, Augusto Rojas-Martinez
Publikováno v:
Human Mutation, 42, 1066-1078
Human Mutation, 42, 8, pp. 1066-1078
Thieme, F, Henschel, L, Hammond, N L, Ishorst, N, Hausen, J, Adamson, A D, Biedermann, A, Bowes, J, Zieger, H K, Maj, C, Kruse, T, Buness, A, Hoischen, A, Gilissen, C, Kreusch, T, Jäger, A, Gölz, L, Braumann, B, Aldhorae, K, Rojas-Martinez, A, Krawitz, P M, Mangold, E, Dixon, M J & Ludwig, K U 2021, ' Extending the allelic spectrum at noncoding risk loci of orofacial clefting ', Human Mutation, vol. 42, no. 8, pp. 1066-1078 . https://doi.org/10.1002/humu.24219
Human Mutation, 42, 8, pp. 1066-1078
Thieme, F, Henschel, L, Hammond, N L, Ishorst, N, Hausen, J, Adamson, A D, Biedermann, A, Bowes, J, Zieger, H K, Maj, C, Kruse, T, Buness, A, Hoischen, A, Gilissen, C, Kreusch, T, Jäger, A, Gölz, L, Braumann, B, Aldhorae, K, Rojas-Martinez, A, Krawitz, P M, Mangold, E, Dixon, M J & Ludwig, K U 2021, ' Extending the allelic spectrum at noncoding risk loci of orofacial clefting ', Human Mutation, vol. 42, no. 8, pp. 1066-1078 . https://doi.org/10.1002/humu.24219
Contains fulltext : 237830.pdf (Publisher’s version ) (Open Access) Genome-wide association studies (GWAS) have generated unprecedented insights into the genetic etiology of orofacial clefting (OFC). The moderate effect sizes of associated noncodin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::684f28dc94ddcaa602e058ea27690078
https://doi.org/10.1002/humu.24219
https://doi.org/10.1002/humu.24219