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Rodrigo T Calado

Showing results (61-70 of 144) with videos related to

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Blood|February 11, 2012
Human telomere disease due to disruption of the CCAAT box of the TERC promoterAnna M Aalbers, Sachiko Kajigaya, Marry M van den Heuvel-Eibrink, et al.
Haematologica|September 2, 2004
Lack of mutations in the human telomerase RNA component (hTERC) gene in Fanconi's anemiaRodrigo T Calado, Maria-Carolina Pintão, Vanderson Rocha, et al.
Hepatology (Baltimore, Md.)|April 27, 2011
Constitutional telomerase mutations are genetic risk factors for cirrhosisRodrigo T Calado, Jennifer Brudno, Paulomi Mehta, et al.
Journal of the Peripheral Nervous System : JPNS|June 14, 2024
Monoclonal gammopathy-associated peripheral neuropathies: Uncovering pearls and challengesTrajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Blood|May 5, 2007
Mutations in the SBDS gene in acquired aplastic anemiaRodrigo T Calado, Solomon A Graf, Keisha L Wilkerson, et al.
Plos One|November 26, 2009
A spectrum of severe familial liver disorders associate with telomerase mutationsRodrigo T Calado, Joshua A Regal, David E Kleiner, et al.
American Journal of Hematology|February 8, 2016
Acquired TERT promoter mutations stimulate TERT transcription in mantle cell lymphomaJulieta Panero, Raquel M Alves-Paiva, Alejandro Roisman, et al.
Blood|November 20, 2014
Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemiaBogdan Dumitriu, Xingmin Feng, Danielle M Townsley, et al.
Blood|September 23, 2006
Functional characterization of natural telomerase mutations found in patients with hematologic disordersZhong-Tao Xin, Adam D Beauchamp, Rodrigo T Calado, et al.
Blood|October 3, 2013
Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemiaMajed J Dasouki, Syed K Rafi, Adam J Olm-Shipman, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
Blood|February 11, 2012
Human telomere disease due to disruption of the CCAAT box of the TERC promoterAnna M Aalbers, Sachiko Kajigaya, Marry M van den Heuvel-Eibrink, et al.
Haematologica|September 2, 2004
Lack of mutations in the human telomerase RNA component (hTERC) gene in Fanconi's anemiaRodrigo T Calado, Maria-Carolina Pintão, Vanderson Rocha, et al.
Hepatology (Baltimore, Md.)|April 27, 2011
Constitutional telomerase mutations are genetic risk factors for cirrhosisRodrigo T Calado, Jennifer Brudno, Paulomi Mehta, et al.
Journal of the Peripheral Nervous System : JPNS|June 14, 2024
Monoclonal gammopathy-associated peripheral neuropathies: Uncovering pearls and challengesTrajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Blood|May 5, 2007
Mutations in the SBDS gene in acquired aplastic anemiaRodrigo T Calado, Solomon A Graf, Keisha L Wilkerson, et al.
Plos One|November 26, 2009
A spectrum of severe familial liver disorders associate with telomerase mutationsRodrigo T Calado, Joshua A Regal, David E Kleiner, et al.
American Journal of Hematology|February 8, 2016
Acquired TERT promoter mutations stimulate TERT transcription in mantle cell lymphomaJulieta Panero, Raquel M Alves-Paiva, Alejandro Roisman, et al.
Blood|November 20, 2014
Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemiaBogdan Dumitriu, Xingmin Feng, Danielle M Townsley, et al.
Blood|September 23, 2006
Functional characterization of natural telomerase mutations found in patients with hematologic disordersZhong-Tao Xin, Adam D Beauchamp, Rodrigo T Calado, et al.
Blood|October 3, 2013
Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemiaMajed J Dasouki, Syed K Rafi, Adam J Olm-Shipman, et al.
Pageof 15