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The American Journal of Forensic Medicine and Pathology|January 8, 2021
New Mexico's COVID-19 ExperienceNicole R Jackson, Karen Zeigler, Mary Torrez, et al.
Lancet (London, England)|February 6, 1993
Localisation of atopy and beta subunit of high-affinity IgE receptor (Fc epsilon RI) on chromosome 11qA J Sandford, T Shirakawa, M F Moffatt, et al.
Breast Cancer Research : BCR|October 31, 2023
mTOR inhibition abrogates human mammary stem cells and early breast cancer progression markersHakim Bouamar, Larry Esteban Broome, Kate Ida Lathrop, et al.
Journal of Public Health Management and Practice : JPHMP|March 17, 2021
Access to Contraceptive Services in Puerto Rico: An Analysis of Policy and Practice Change Strategies, 2015-2018Lisa Romero, Rosa M Corrada-Rivera, Xavier Huertas-Pagan, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health|May 8, 2020
Program Fidelity and Patient Satisfaction among Women Served by the Zika Contraception Access Network Program in Puerto RicoLauren B Zapata, Lisa Romero, Maria I Rivera, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 2011
Genetic and functional evaluation of MITF as a candidate gene for cutaneous melanoma predisposition in pigsEmmanuelle Bourneuf, Zhi-Qiang Du, Jordi Estellé, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 11, 2012
Validating deaths reported in the Foodborne Diseases Active Surveillance Network (FoodNet): are all deaths being captured?Karunya Manikonda, Amanda Palmer, Katie Wymore, et al.
Immunogenetics|February 24, 2006
Associations of the IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFN (gamma) R1 cytokine receptor genes with AIDS progression in a French AIDS cohortHervé Do, Alexandre Vasilescu, Gora Diop, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activityE Petit, M Huber, A Rochat, et al.
American Journal of Human Genetics|October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formationA Hovnanian, A Rochat, C Bodemer, et al.
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