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pro vyhledávání: '"Leeyean Wong"'
Publikováno v:
Dev Biol
Combined methylmalonic acidemia and homocystinuria, cblC type, is the most common inherited disorder of cobalamin metabolism and is characterized by severe fetal developmental defects primarily impacting the central nervous system, hematopoietic syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b43c14e39c3fdef177191829a5d062ce
https://europepmc.org/articles/PMC7669717/
https://europepmc.org/articles/PMC7669717/
Autor:
Mary E. Dickinson, Melissa L. McElwee, Marion Dejosez, Leeyean Wong, Chih-Wei Hsu, Alan R. Burns, Min Zhang, Thomas P. Zwaka, Ross A. Poché, James F. Martin, Elda M. Rueda, Donald A. Fox, Xuefei Tong
Publikováno v:
Cell Reports. 14(7):1684-1697
SummaryA fundamental principle governing organ size and function is the fine balance between cell proliferation and cell differentiation. Here, we identify RONIN (THAP11) as a key transcriptional regulator of retinal progenitor cell (RPC) proliferati
Autor:
Mary E, Dickinson, Ann M, Flenniken, Xiao, Ji, Lydia, Teboul, Michael D, Wong, Jacqueline K, White, Terrence F, Meehan, Wolfgang J, Weninger, Henrik, Westerberg, Hibret, Adissu, Candice N, Baker, Lynette, Bower, James M, Brown, L Brianna, Caddle, Francesco, Chiani, Dave, Clary, James, Cleak, Mark J, Daly, James M, Denegre, Brendan, Doe, Mary E, Dolan, Sarah M, Edie Helmut Fuchs, Valerie, Gailus-Durner, Antonella, Galli, Alessia, Gambadoro, Juan, Gallegos, Shiying, Guo, Neil R, Horner, Chih-Wei, Hsu, Sara J, Johnson, Sowmya, Kalaga, Lance C, Keith, Louise, Lanoue, Thomas N, Lawson, Monkol, Lek, Manuel, Mark, Susan, Marschall, Jeremy, Mason, Melissa L, McElwee, Susan Newbigging Lauryl M J, Nutter, Kevin A, Peterson, Ramiro, Ramirez-Solis, Douglas J, Rowland, Edward, Ryder, Kaitlin E, Samocha, John R, Seavitt, Mohammed, Selloum, Zsombor, Szoke-Kovacs, Masaru, Tamura, Amanda G, Trainor, Ilinca, Tudose, Shigeharu, Wakana, Jonathan, Warren, Olivia, Wendling, David B, West, Leeyean, Wong, Atsushi, Yoshiki, Wolfgang, Wurst, Daniel G, MacArthur, Glauco P, Tocchini-Valentini, Xiang, Gao, Paul, Flicek, Allan, Bradley, William C, Skarnes, Monica J, Justice, Helen E, Parkinson, Mark, Moore, Sara, Wells, Robert E, Braun, Karen L, Svenson, Martin Hrabe, de Angelis, Yann, Herault, Tim, Mohun, Ann-Marie, Mallon, R Mark, Henkelman, Steve D M, Brown, David J, Adams, K C Kent, Lloyd, Colin, McKerlie, Arthur L, Beaudet, Maja Bućan Stephen A, Murray
Publikováno v:
Nature
Approximately one third of all mammalian genes are essential for life. Phenotypes resulting from mouse knockouts of these genes have provided tremendous insight into gene function and congenital disorders. As part of the International Mouse Phenotypi
Autor:
Henrik Westerberg, Yann Herault, Colin McKerlie, Candice N. Baker, Dave Clary, William C. Skarnes, Hibret A. Adissu, Thomas N. Lawson, Monica J. Justice, R. Mark Henkelman, Monkol Lek, Helen Parkinson, Timothy J. Mohun, Sarah M. Edie, Paul Flicek, Francesco Chiani, Steve D.M. Brown, Martin Hrabé de Angelis, Mary E. Dolan, Chih-Wei Hsu, L. Brianna Caddle, Sara Wells, John R. Seavitt, Wolfgang Weninger, James M. Brown, Neil R. Horner, Zsombor Szoke-Kovacs, Louise Lanoue, Jacqueline K. White, Lauryl M. J. Nutter, Shiying Guo, Allan Bradley, Jonathan Warren, Ann M. Flenniken, Manuel Mark, Kevin A. Peterson, Kaitlin E. Samocha, Douglas J. Rowland, Daniel G. MacArthur, Ann-Marie Mallon, Maja Bucan, Amanda G. Trainor, Susan Newbigging, Ramiro Ramirez-Solis, Glauco P. Tocchini-Valentini, Shigeharu Wakana, Ilinca Tudose, Olivia Wendling, Edward Ryder, Lydia Teboul, Melissa L. McElwee, Kevin C K Lloyd, Terrence F. Meehan, David B. West, Stephen A. Murray, Valerie Gailus-Durner, Lance C. Keith, Mark J. Daly, Lynette Bower, Juan Gallegos, Masaru Tamura, Helmut Fuchs, Susan Marschall, Mark W. Moore, Karen L. Svenson, Sara Johnson, David J. Adams, Xiang Gao, Robert E. Braun, Mohammed Selloum, Xiao Ji, Michael D. Wong, Atsushi Yoshiki, Alessia Gambadoro, James M. Denegre, Leeyean Wong, Jeremy Mason, Antonella Galli, Sowmya Kalaga, Arthur L. Beaudet, James Cleak, Brendan Doe, Mary E. Dickinson
Publikováno v:
Nature (Lond.) 537 (2016): 508–514. doi:10.1038/nature19356
info:cnr-pdr/source/autori:Mary E. Dickinson,Ann M. Flenniken,Xiao Ji,Lydia Teboul,Michael D. Wong,Jacqueline K. White,Terrence F. Meehan,Wolfgang J. Weninger,Henrik Westerberg,Hibret Adissu, Candice N. Baker,Lynette Bower,James M. Brown,L. Brianna Caddle,Francesco Chiani, Dave Clary,James Cleak,Mark J. Daly,James M. Denegre,Brendan Doe,Mary E. Dolan, Sarah M. Edie,Helmut Fuchs,Valerie Gailus-Durner,Antonella Galli,Alessia Gambadoro, Juan Gallegos,Shiying Guo,Neil R. Horner,Chih-Wei Hsu,Sara J. Johnson,Sowmya Kalaga,Lance C. Keith,Louise Lanoue,Thomas N. Lawson,Monkol Lek,Manuel Mark, Susan Marschall,Jeremy Mason,Melissa L. McElwee,Susan Newbigging,Lauryl M. J. Nutter,Kevin A. Peterson,Ramiro Ramirez-Solis,Douglas J. Rowland,Edward Ryder, Kaitlin E. Samocha,John R. Seavitt,Mohammed Selloum,Zsombor Szoke-Kovacs,Masaru Tamura,Amanda G. Trainor,Ilinca Tudose,Shigeharu Wakana,Jonathan Warren,Olivia Wendling,David B. West,Leeyean Wong,Atsushi Yoshiki,The International Mouse Phenotyping Consortium,Daniel G. MacArthur,Glauco P. Tocchini-Valentini,Xiang Gao, Paul Flicek,Allan Bradley,William C. Skarnes,Monica J. Justice,Helen E. Parkinson,Mark Moore,Sara Wells,Robert E. Braun,Karen L. Svenson,Martin Hrabe de Angelis,Yann Herault,Tim Mohun,Ann-Marie Mallon,R. Mark Henkelman,Steve D. M. Brown,David J. Adams,K. C. Kent Lloyd,Colin McKerlie,Arthur L. Beaudet,Maja Bu?an& Stephen A. Murray/titolo:High-throughput discovery of novel developmental phenotypes./doi:10.1038%2Fnature19356/rivista:Nature (Lond.)/anno:2016/pagina_da:508/pagina_a:514/intervallo_pagine:508–514/volume:537
Nature 537, 508-514 (2016)
info:cnr-pdr/source/autori:Mary E. Dickinson,Ann M. Flenniken,Xiao Ji,Lydia Teboul,Michael D. Wong,Jacqueline K. White,Terrence F. Meehan,Wolfgang J. Weninger,Henrik Westerberg,Hibret Adissu, Candice N. Baker,Lynette Bower,James M. Brown,L. Brianna Caddle,Francesco Chiani, Dave Clary,James Cleak,Mark J. Daly,James M. Denegre,Brendan Doe,Mary E. Dolan, Sarah M. Edie,Helmut Fuchs,Valerie Gailus-Durner,Antonella Galli,Alessia Gambadoro, Juan Gallegos,Shiying Guo,Neil R. Horner,Chih-Wei Hsu,Sara J. Johnson,Sowmya Kalaga,Lance C. Keith,Louise Lanoue,Thomas N. Lawson,Monkol Lek,Manuel Mark, Susan Marschall,Jeremy Mason,Melissa L. McElwee,Susan Newbigging,Lauryl M. J. Nutter,Kevin A. Peterson,Ramiro Ramirez-Solis,Douglas J. Rowland,Edward Ryder, Kaitlin E. Samocha,John R. Seavitt,Mohammed Selloum,Zsombor Szoke-Kovacs,Masaru Tamura,Amanda G. Trainor,Ilinca Tudose,Shigeharu Wakana,Jonathan Warren,Olivia Wendling,David B. West,Leeyean Wong,Atsushi Yoshiki,The International Mouse Phenotyping Consortium,Daniel G. MacArthur,Glauco P. Tocchini-Valentini,Xiang Gao, Paul Flicek,Allan Bradley,William C. Skarnes,Monica J. Justice,Helen E. Parkinson,Mark Moore,Sara Wells,Robert E. Braun,Karen L. Svenson,Martin Hrabe de Angelis,Yann Herault,Tim Mohun,Ann-Marie Mallon,R. Mark Henkelman,Steve D. M. Brown,David J. Adams,K. C. Kent Lloyd,Colin McKerlie,Arthur L. Beaudet,Maja Bu?an& Stephen A. Murray/titolo:High-throughput discovery of novel developmental phenotypes./doi:10.1038%2Fnature19356/rivista:Nature (Lond.)/anno:2016/pagina_da:508/pagina_a:514/intervallo_pagine:508–514/volume:537
Nature 537, 508-514 (2016)
Approximately one-third of all mammalian genes are essential for life. Phenotypes resulting from knockouts of these genes in mice have provided tremendous insight into gene function and congenital disorders. As part of the International Mouse Phenoty
Publikováno v:
Life Sciences. 86:275-280
To identify proteins with which FolBp1 may interact within lipid rafts in tissue derived from embryonic orofacial tissue.A yeast two-hybrid screen of a cDNA library, derived from orofacial tissue from gestational day 11 to 13 mouse embryos, was condu
Autor:
Steve D.M. Brown, L. Brianna Caddle, Valerie Gailus-Durner, Xiao Ji, Sowmya Kalaga, Mark J. Daly, Kevin C K Lloyd, Susan Newbigging Lauryl M. J. Nutter, Jeremy Mason, Martin Hrabé de Angelis, Ann-Marie Mallon, Helen Parkinson, Paul Flicek, Timothy J. Mohun, Lynette Bower, Shiying Guo, Edward Ryder, Ramiro Ramirez-Solis, Ilinca Tudose, William C. Skarnes, Hibret A. Adissu, Francesco Chiani, Lance C. Keith, Maja Bućan Stephen A. Murray, Susan Marschall, John R. Seavitt, Henrik Westerberg, Chih-Wei Hsu, Terrence F. Meehan, David B. West, Ann M. Flenniken, Mohammed Selloum, Karen L. Svenson, Daniel G. MacArthur, Allan Bradley, Zsombor Szoke-Kovacs, Alessia Gambadoro, Glauco P. Tocchini-Valentini, James M. Denegre, Leeyean Wong, Neil R. Horner, Amanda G. Trainor, Mary E. Dickinson, James M. Brown, Shigeharu Wakana, Kevin A. Peterson, Lydia Teboul, Michael D. Wong, Atsushi Yoshiki, Robert Braun, Mark W. Moore, Masaru Tamura, Jacqueline K. White, Mary E. Dolan, Manuel Mark, David J. Adams, Kaitlin E. Samocha, Thomas N. Lawson, Monica J. Justice, Candice N. Baker, Wolfgang Weninger, Melissa L. McElwee, Sara Wells, Olivia Wendling, Douglas J. Rowland, R. Mark Henkelman, Juan Gallegos, Sara Johnson, Colin McKerlie, Wolfgang Wurst, Dave Clary, Xiang Gao, Louise Lanoue, Monkol Lek, Sarah M. Edie Helmut Fuchs, Jonathan Warren, Yann Herault, Arthur L. Beaudet, James Cleak, Brendan Doe, Antonella Galli
Publikováno v:
Nature. 551:398-398
Nature 537, 508–514 (2016); doi:10.1038/nature19356 In this Article, the author Wolfgang Wurst was erroneously omitted from the author list. They are associated with the affiliations: HelmholtzZentrum Munich, Institute of Developmental Genetics, 85
Autor:
Steve L. Brody, Adriana Cavender, Brad A. Amendt, Melanie Amen, Rena N. D'Souza, Leeyean Wong, Mikael Åkerlund, Tord A. Hjalt, Shankar Rengasamy Venugopalan, Jianbo Wang
Publikováno v:
Human Molecular Genetics. 17:3643-3654
Axenfeld-Rieger syndrome (ARS) patients with PITX2 point mutations exhibit a wide range of clinical features including mild craniofacial dysmorphism and dental anomalies. Identifying new PITX2 targets and transcriptional mechanisms are important to u
Publikováno v:
Microscopy and Microanalysis. 22:1024-1025