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Showing results (301-310 of 362) with videos related to

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Anemia|June 16, 2012
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba MennonitesYne de Vries, Nikki Lwiwski, Marieke Levitus, et al.
Science Advances|April 18, 2020
Germline mutation of <i>MDM4</i>, a major p53 regulator, in a familial syndrome of defective telomere maintenanceEléonore Toufektchan, Vincent Lejour, Romane Durand, et al.
Blood|July 2, 2011
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assayKajal Biswas, Ranabir Das, Blanche P Alter, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|April 30, 2013
The use of haematopoietic stem cell transplantation in Fanconi anaemia patients: a survey of decision making among families in the US and CanadaSadie P Hutson, Paul K J Han, Jada G Hamilton, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|June 8, 2018
Chromosomal Aberrations and Survival after Unrelated Donor Hematopoietic Stem Cell Transplant in Patients with Fanconi AnemiaYoujin Wang, Weiyin Zhou, Blanche P Alter, et al.
International Journal of Molecular Sciences|August 15, 2017
Correlation of Leukocyte Telomere Length Measurement Methods in Patients with Dyskeratosis Congenita and in Their Unaffected RelativesPayal P Khincha, Casey L Dagnall, Belynda Hicks, et al.
The EMBO Journal|September 16, 2020
Re-equilibration of imbalanced NAD metabolism ameliorates the impact of telomere dysfunctionChongkui Sun, Kun Wang, Amanda J Stock, et al.
Leukemia|May 1, 1993
Effects of treatment with 5-azacytidine on the in vivo and in vitro hematopoiesis in patients with myelodysplastic syndromesL R Silverman, J F Holland, R S Weinberg, et al.
Pediatric Neurology|January 27, 2016
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-UpAshley M Burris, Bari J Ballew, Joshua B Kentosh, et al.
Genes & Development|September 20, 2014
Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Pageof 37

Showing results (301-310 of 362) with videos related to

Sort By:
Pageof 37
Anemia|June 16, 2012
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba MennonitesYne de Vries, Nikki Lwiwski, Marieke Levitus, et al.
Science Advances|April 18, 2020
Germline mutation of <i>MDM4</i>, a major p53 regulator, in a familial syndrome of defective telomere maintenanceEléonore Toufektchan, Vincent Lejour, Romane Durand, et al.
Blood|July 2, 2011
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assayKajal Biswas, Ranabir Das, Blanche P Alter, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|April 30, 2013
The use of haematopoietic stem cell transplantation in Fanconi anaemia patients: a survey of decision making among families in the US and CanadaSadie P Hutson, Paul K J Han, Jada G Hamilton, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|June 8, 2018
Chromosomal Aberrations and Survival after Unrelated Donor Hematopoietic Stem Cell Transplant in Patients with Fanconi AnemiaYoujin Wang, Weiyin Zhou, Blanche P Alter, et al.
International Journal of Molecular Sciences|August 15, 2017
Correlation of Leukocyte Telomere Length Measurement Methods in Patients with Dyskeratosis Congenita and in Their Unaffected RelativesPayal P Khincha, Casey L Dagnall, Belynda Hicks, et al.
The EMBO Journal|September 16, 2020
Re-equilibration of imbalanced NAD metabolism ameliorates the impact of telomere dysfunctionChongkui Sun, Kun Wang, Amanda J Stock, et al.
Leukemia|May 1, 1993
Effects of treatment with 5-azacytidine on the in vivo and in vitro hematopoiesis in patients with myelodysplastic syndromesL R Silverman, J F Holland, R S Weinberg, et al.
Pediatric Neurology|January 27, 2016
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-UpAshley M Burris, Bari J Ballew, Joshua B Kentosh, et al.
Genes & Development|September 20, 2014
Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Pageof 37