Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tom Enbar"'
Autor:
Jessica M. Livingston, Tina T. Lee, Tom Enbar, Emerson Daniele, Clara M. Phillips, Alexandra Krassikova, K. W. Annie Bang, Ines Kortebi, Brennan W. Donville, Omadyor S. Ibragimov, Nadia Sachewsky, Daniela Lozano Casasbuenas, Arman Olfat, Cindi M. Morshead
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 663 (2024)
Stroke is the leading cause of adult disability worldwide. The majority of stroke survivors are left with devastating functional impairments for which few treatment options exist. Recently, a number of studies have used ectopic expression of transcri
Externí odkaz:
https://doaj.org/article/bd79272862d64e0c9a0bb4df21383a27
Autor:
Nicolas Waespe, Santhosh Dhanraj, Manju Wahala, Elena Tsangaris, Tom Enbar, Bozana Zlateska, Hongbing Li, Robert J. Klaassen, Conrad V. Fernandez, Geoff D. E. Cuvelier, John K. Wu, Yves D. Pastore, Mariana Silva, Jeffrey H. Lipton, Joseé Brossard, Bruno Michon, Sharon Abish, MacGregor Steele, Roona Sinha, Mark J. Belletrutti, Vicky R. Breakey, Lawrence Jardine, Lisa Goodyear, Liat Kofler, Michaela Cada, Lillian Sung, Mary Shago, Stephen W. Scherer, Yigal Dror
Publikováno v:
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-8 (2017)
Blood disorders: impact of genomic structural variation Copy number variation in patients with inherited bone marrow failure syndromes (IBMFSs) is associated with more severe clinical symptoms. In addition to persistently low levels of red blood cell
Externí odkaz:
https://doaj.org/article/fab055366f7246f79c31483ee2eaa142
Autor:
Maryam Faiz, Ines Kortebi, Omadyor Ibragimov, Jessica Livingston, Emerson Daniele, Tina Lee, K.W. Annie Bang, Alexandra Krassikova, Cindi M. Morshead, Tom Enbar, Nadia Sachewsky, Clara Phillips, Brennan Donville
Stroke is the leading cause of adult disability with few treatment options for stroke survivors. Astrocyte reprogramming to neurons enables the targeted in vivo generation of new cells at the site of injury and represents a novel approach for brain r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42cc97d27f65cab93c8e1cf092e5d95b
Autor:
Roona Sinha, Conrad V. Fernandez, John K. Wu, Nicolas Waespe, Geoff D.E. Cuvelier, MacGregor Steele, Hongbing Li, Mariana Silva, Tom Enbar, Yigal Dror, Lawrence Jardine, Elena Tsangaris, Vicky R. Breakey, Jeffrey H. Lipton, Bozana Zlateska, Stephen W. Scherer, Josee Brossard, Santhosh Dhanraj, Bruno Michon, Robert J. Klaassen, Manju Wahala, Sharon Abish, Mark Belletrutti, Liat Kofler, Michaela Cada, Mary Shago, Yves D. Pastore, Lillian Sung, Lisa Goodyear
Publikováno v:
Paediatrics Publications
NPJ Genomic Medicine
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-8 (2017)
NPJ Genomic Medicine
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-8 (2017)
Inherited bone marrow failure syndromes comprise a genetically heterogeneous group of diseases with hematopoietic failure and a wide array of physical malformations. Copy number variants were reported in some inherited bone marrow failure syndromes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6d7d6110d94bd4feb3bf9bbcb88bb9
https://ir.lib.uwo.ca/context/paedpub/article/1054/viewcontent/The_clinical_impact_of_copy_number_variants_in_inherited_bone.pdf
https://ir.lib.uwo.ca/context/paedpub/article/1054/viewcontent/The_clinical_impact_of_copy_number_variants_in_inherited_bone.pdf
Autor:
Mark Belletrutti, Lisa Goodyear, Hongbing Li, Nicolas Waespe, Michaela Cada, Mary Shago, John K. Wu, Robert J. Klaassen, Liat Kofler, Yigal Dror, Manju Wahala, Mariana Silva, Lawrence Jardine, Rochelle Yanofsky, Ibrahim Ghemlas, MacGregor Steele, Lillian Sung, Stephen W. Scherer, Bozana Zlateska, Santhosh Dhanraj, Roona Sinha, Bruno Michon, Vicky R. Breakey, Tom Enbar, Yves D. Pastore, Josee Brossard, Sharon Abish, Conrad V. Fernandez, Jeffrey H. Lipton
Publikováno v:
Blood. 126:2416-2416
Background. Inherited bone marrow failure syndromes (IBMFSs) comprise a genetically heterogeneous group of diseases with hematopoietic failure and varying degrees of physical malformations. The diagnosis of an IBMFS and categorizing the specific synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d6b7405ddf8c64254ed2cf907cd6464
https://doi.org/10.1182/blood.v126.23.2416.2416
https://doi.org/10.1182/blood.v126.23.2416.2416