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American Journal of Medical Genetics. Part A
|
April 1, 2022
The germline p53 activation syndrome: A new patient further refines the clinical phenotype
Runjun D Kumar, Mustafa Tosur, Seema R Lalani, et al.
Pediatric Blood & Cancer
|
April 22, 2016
Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis
Nya D Nelson, Andrea Marcogliese, Katie Bergstrom, et al.
Pediatric Blood & Cancer
|
May 4, 2019
Severe therapy-related toxicities after treatment for Hodgkin lymphoma due to a pathogenic TERT variant and shortened telomeres
Jennifer E Agrusa, Alison A Bertuch, Courtney D DiNardo, et al.
Blood
|
March 30, 2013
A homozygous telomerase T-motif variant resulting in markedly reduced repeat addition processivity in siblings with Hoyeraal Hreidarsson syndrome
Maria M Gramatges, Xiaodong Qi, Ghadir S Sasa, et al.
Genetics
|
August 5, 2009
The association of yKu with subtelomeric core X sequences prevents recombination involving telomeric sequences
Marcus E Marvin, Marion M Becker, Pawan Noel, et al.
Blood Advances
|
June 2, 2018
Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenita
Payal P Khincha, Alison A Bertuch, Shahinaz M Gadalla, et al.
Genes & Development
|
August 26, 2011
A role for heterochromatin protein 1γ at human telomeres
Silvia Canudas, Benjamin R Houghtaling, Monica Bhanot, et al.
Plos Genetics
|
August 20, 2011
Ku must load directly onto the chromosome end in order to mediate its telomeric functions
Christopher R Lopez, Albert Ribes-Zamora, Sandra M Indiviglio, et al.
BMC Genomics
|
November 27, 2012
An S/T-Q cluster domain census unveils new putative targets under Tel1/Mec1 control
Hannah C Cheung, F Anthony San Lucas, Stephanie Hicks, et al.
American Journal of Medical Genetics. Part A
|
June 23, 2021
Expansion of the clinical phenotype of GALE deficiency
Rebecca Markovitz, Nichole Owen, Lisa Forbes Satter, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 77) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics. Part A
|
April 1, 2022
The germline p53 activation syndrome: A new patient further refines the clinical phenotype
Runjun D Kumar, Mustafa Tosur, Seema R Lalani, et al.
Pediatric Blood & Cancer
|
April 22, 2016
Thrombopoietin Measurement as a Key Component in the Evaluation of Pediatric Thrombocytosis
Nya D Nelson, Andrea Marcogliese, Katie Bergstrom, et al.
Pediatric Blood & Cancer
|
May 4, 2019
Severe therapy-related toxicities after treatment for Hodgkin lymphoma due to a pathogenic TERT variant and shortened telomeres
Jennifer E Agrusa, Alison A Bertuch, Courtney D DiNardo, et al.
Blood
|
March 30, 2013
A homozygous telomerase T-motif variant resulting in markedly reduced repeat addition processivity in siblings with Hoyeraal Hreidarsson syndrome
Maria M Gramatges, Xiaodong Qi, Ghadir S Sasa, et al.
Genetics
|
August 5, 2009
The association of yKu with subtelomeric core X sequences prevents recombination involving telomeric sequences
Marcus E Marvin, Marion M Becker, Pawan Noel, et al.
Blood Advances
|
June 2, 2018
Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenita
Payal P Khincha, Alison A Bertuch, Shahinaz M Gadalla, et al.
Genes & Development
|
August 26, 2011
A role for heterochromatin protein 1γ at human telomeres
Silvia Canudas, Benjamin R Houghtaling, Monica Bhanot, et al.
Plos Genetics
|
August 20, 2011
Ku must load directly onto the chromosome end in order to mediate its telomeric functions
Christopher R Lopez, Albert Ribes-Zamora, Sandra M Indiviglio, et al.
BMC Genomics
|
November 27, 2012
An S/T-Q cluster domain census unveils new putative targets under Tel1/Mec1 control
Hannah C Cheung, F Anthony San Lucas, Stephanie Hicks, et al.
American Journal of Medical Genetics. Part A
|
June 23, 2021
Expansion of the clinical phenotype of GALE deficiency
Rebecca Markovitz, Nichole Owen, Lisa Forbes Satter, et al.
Page
of 8