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Anemia
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June 16, 2012
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites
Yne 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 maintenance
Eléonore 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 assay
Kajal 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 Canada
Sadie 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 Anemia
Youjin 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 Relatives
Payal 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 dysfunction
Chongkui 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 syndromes
L 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-Up
Ashley 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 TPP1
Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Page
of 37
Search research articles
Search
Showing results (301-310 of 362) with videos related to
Sort By:
Page
of 37
Anemia
|
June 16, 2012
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites
Yne 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 maintenance
Eléonore 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 assay
Kajal 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 Canada
Sadie 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 Anemia
Youjin 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 Relatives
Payal 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 dysfunction
Chongkui 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 syndromes
L 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-Up
Ashley 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 TPP1
Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Page
of 37