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Steven R Ellis

Showing results (21-30 of 49) with videos related to

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Blood|September 23, 2006
Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunitsJohan Flygare, Anna Aspesi, Joshua C Bailey, et al.
Pediatric Blood & Cancer|September 22, 2012
Impaired growth, hematopoietic colony formation, and ribosome maturation in human cells depleted of Shwachman-Diamond syndrome protein SBDSGulay Sezgin, Adrianna L Henson, Abdallah Nihrane, et al.
Pediatric Blood & Cancer|January 24, 2014
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotypeSara Parrella, Anna Aspesi, Paola Quarello, et al.
The Journal of Comparative Neurology|July 3, 2013
IB4-binding sensory neurons in the adult rat express a novel 3' UTR-extended isoform of CaMK4 that is associated with its localization to axonsBenjamin J Harrison, Robert M Flight, Cynthia Gomes, et al.
Blood|November 3, 2011
Ribosomal protein gene deletions in Diamond-Blackfan anemiaJason E Farrar, Adrianna Vlachos, Eva Atsidaftos, et al.
Plos One|February 22, 2014
p53-Independent cell cycle and erythroid differentiation defects in murine embryonic stem cells haploinsufficient for Diamond Blackfan anemia-proteins: RPS19 versus RPL5Sharon A Singh, Tracie A Goldberg, Adrianna L Henson, et al.
Nature|January 19, 2008
Identification of RPS14 as a 5q- syndrome gene by RNA interference screenBenjamin L Ebert, Jennifer Pretz, Jocelyn Bosco, et al.
EMBO Molecular Medicine|March 8, 2017
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with <i>TP53</i> mutationsRam Ajore, David Raiser, Marie McConkey, et al.
Frontiers in Genetics|December 29, 2022
Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiationNoemy Piantanida, Marta La Vecchia, Marika Sculco, et al.
Human Mutation|May 17, 2018
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond-Blackfan anemiaAnna Aspesi, Marta Betti, Marika Sculco, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Blood|September 23, 2006
Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunitsJohan Flygare, Anna Aspesi, Joshua C Bailey, et al.
Pediatric Blood & Cancer|September 22, 2012
Impaired growth, hematopoietic colony formation, and ribosome maturation in human cells depleted of Shwachman-Diamond syndrome protein SBDSGulay Sezgin, Adrianna L Henson, Abdallah Nihrane, et al.
Pediatric Blood & Cancer|January 24, 2014
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotypeSara Parrella, Anna Aspesi, Paola Quarello, et al.
The Journal of Comparative Neurology|July 3, 2013
IB4-binding sensory neurons in the adult rat express a novel 3' UTR-extended isoform of CaMK4 that is associated with its localization to axonsBenjamin J Harrison, Robert M Flight, Cynthia Gomes, et al.
Blood|November 3, 2011
Ribosomal protein gene deletions in Diamond-Blackfan anemiaJason E Farrar, Adrianna Vlachos, Eva Atsidaftos, et al.
Plos One|February 22, 2014
p53-Independent cell cycle and erythroid differentiation defects in murine embryonic stem cells haploinsufficient for Diamond Blackfan anemia-proteins: RPS19 versus RPL5Sharon A Singh, Tracie A Goldberg, Adrianna L Henson, et al.
Nature|January 19, 2008
Identification of RPS14 as a 5q- syndrome gene by RNA interference screenBenjamin L Ebert, Jennifer Pretz, Jocelyn Bosco, et al.
EMBO Molecular Medicine|March 8, 2017
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with <i>TP53</i> mutationsRam Ajore, David Raiser, Marie McConkey, et al.
Frontiers in Genetics|December 29, 2022
Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiationNoemy Piantanida, Marta La Vecchia, Marika Sculco, et al.
Human Mutation|May 17, 2018
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond-Blackfan anemiaAnna Aspesi, Marta Betti, Marika Sculco, et al.
Pageof 5