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MG132 Induces Progerin Clearance and Improves Disease Phenotypes in HGPS-like Patients' Cells.
Cells. 2022 Feb 10;11(4):610. doi: 10.3390/cells11040610.
Cells. 2022.
PMID: 35203262
Free PMC article.
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
Mirabello L, Zhu B, Koster R, Karlins E, Dean M, Yeager M, Gianferante M, Spector LG, Morton LM, Karyadi D, Robison LL, Armstrong GT, Bhatia S, Song L, Pankratz N, Pinheiro M, Gastier-Foster JM, Gorlick R, de Toledo SRC, Petrilli AS, Patino-Garcia A, Lecanda F, Gutierrez-Jimeno M, Serra M, Hattinger C, Picci P, Scotlandi K, Flanagan AM, Tirabosco R, Amary MF, Kurucu N, Ilhan IE, Ballinger ML, Thomas DM, Barkauskas DA, Mejia-Baltodano G, Valverde P, Hicks BD, Zhu B, Wang M, Hutchinson AA, Tucker M, Sampson J, Landi MT, Freedman ND, Gapstur S, Carter B, Hoover RN, Chanock SJ, Savage SA.
Mirabello L, et al. Among authors: mejia baltodano g.
JAMA Oncol. 2020 May 1;6(5):724-734. doi: 10.1001/jamaoncol.2020.0197.
JAMA Oncol. 2020.
PMID: 32191290
Free PMC article.
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Establishment of a specialized laboratory for hemoglobin analysis in Nicaragua.
Pernudy-Ubau A, Puller AC, Mejía-Baltodano G, Rodríguez-Romero W.
Pernudy-Ubau A, et al. Among authors: mejia baltodano g.
Blood Adv. 2018 Nov 30;2(Suppl 1):58-59. doi: 10.1182/bloodadvances.2018GS110337.
Blood Adv. 2018.
PMID: 30504204
Free PMC article.
No abstract available.
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Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family.
Pernudy-Ubau A, Salinas-Molina J, Requenez Y, Ortiz-Lopez M, Puller AC, García-Rosales K, Rodríguez-Estrada A, Rodríguez-Romero W, Mejía-Baltodano G, Luo HY, Chui DHK.
Pernudy-Ubau A, et al. Among authors: mejia baltodano g.
Hemoglobin. 2017 Jan;41(1):50-52. doi: 10.1080/03630269.2017.1302949. Epub 2017 Apr 11.
Hemoglobin. 2017.
PMID: 28395541
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Sex reversal due to Xp disomy by t(X;Y)(p21;q11).
Vasquez AI, Rivera H, Mayorquin A, Mejia-Baltodano G, Escalante A, Sanchez-Corona J.
Vasquez AI, et al. Among authors: mejia baltodano g.
Genet Couns. 1999;10(3):301-4.
Genet Couns. 1999.
PMID: 10546103
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A further microchromosome with centromeric association.
Rivera H, Dominguez MG, Vasquez AI, Mejia-Baltodano G.
Rivera H, et al. Among authors: mejia baltodano g.
Genet Couns. 1997;8(4):323-6.
Genet Couns. 1997.
PMID: 9457502
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A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome.
Mejía-Baltodano G, Bobadilla L, Solís A, Mendoza R, Díaz-Gallardo MY, Barros-Núñez P.
Mejía-Baltodano G, et al.
Genet Couns. 1997;8(4):311-6.
Genet Couns. 1997.
PMID: 9457500
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High recurrence of recombinants in a family with pericentric inversion of chromosome 18.
Mejía-Baltodano G, Bobadilla L, Gonzalez RM, Barros-Núñez P.
Mejía-Baltodano G, et al.
Ann Genet. 1997;40(3):164-8.
Ann Genet. 1997.
PMID: 9401106
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