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Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|December 18, 2007
Crystallization and preliminary X-ray diffraction analysis on the homing endonuclease I-Dmo-I in complex with its target DNAPilar Redondo, Jesús Prieto, Elena Ramos, et al.
International Journal of Behavioral Medicine|June 23, 2025
A Thematic Analysis of Resilient Experiences of People Who Inject Drugs Living with HIV Remaining in HIV CareJulia Lechuga, Gilberto Perez, Valeria Dueñas, et al.
International Microbiology : the Official Journal of the Spanish Society for Microbiology|June 13, 2003
Multiplex PCR for simultaneous detection of enterococcal genes vanA and vanB and staphylococcal genes mecA, ileS-2 and femBElena Ramos-Trujillo, Eduardo Pérez-Roth, Sebastián Méndez-Alvarez, et al.
Genes|January 5, 2018
Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 DiseaseLorena Suarez-Artiles, Ana Perdomo-Ramirez, Elena Ramos-Trujillo, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association|July 19, 2006
Predictors of HIV-related stigma among young people living with HIVDallas Swendeman, Mary Jane Rotheram-Borus, Scott Comulada, et al.
Women'S Health (London, England)|June 3, 2026
I have to keep going for my kids (Tengo que seguir adelante por mis hijos): Migration, wellbeing and the collage narratives of mothers and children in transitMadelyn Primeaux, Sarah Jay, Gulnaz Anjum, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|October 8, 2015
Modeling the Adsorption of Oxalate onto MontmorilloniteM Elena Ramos, Caglayan Emiroglu, David García, et al.
Public Health Reports (Washington, D.C. : 1974)|July 6, 2010
Pasa la voz (spread the word): using women's social networks for HIV education and testingRebeca L Ramos, João B Ferreira-Pinto, Melanie L A Rusch, et al.
Gene|December 22, 2018
Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosisAna Perdomo-Ramirez, Mireia Aguirre, Tinatin Davitaia, et al.
BMC Medical Genetics|January 10, 2019
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterationsAna Perdomo-Ramirez, Marian de Armas-Ortiz, Elena Ramos-Trujillo, et al.
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