Showing results (141-150 of 153) with videos related to
Sort By:
Pageof 16
Chemico-Biological Interactions|March 22, 2024
Thiazolyl-isatin derivatives: Synthesis, in silico studies, in vitro biological profile against breast cancer cells, mRNA expression, P-gp modulation, and interactions of Akt2 and VIM proteinsLuiz Alberto Barros Freitas, Carolina Sousa, Beatriz Silva Lima, et al.Chemmedchem|June 18, 2026
Evaluating the Antitrypanosomatid Activity of Thiazolyl-Isatins: Synthesis, Biological Evaluation, and Electronic Structure Analysis Using the Semiempirical GFN2-xTB MethodLucas Manoel da Silva Sousa, Luiz Alberto Barros Freitas, Vanessa Gouveia de Melo, et al.Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.Revista Brasileira De Terapia Intensiva|October 14, 2014
[Brazilian consensus of monitoring and hemodynamic support - part III: alternative methods for cardiac output monitoring and volemia estimation]Guilherme Schettino, Rezende Ederlon, Ciro Leite Mendes, et al.Revista Brasileira De Terapia Intensiva|October 14, 2014
[Part II: basic hemodynamic monitoring and the use of pulmonary artery catheter]Fernando Suparregui Dias, Ederlon Rezende, Ciro Leite Mendes, et al.Fertility and Sterility|July 22, 2020
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairmentMiriam Cerván-Martín, M Irene Suazo-Sánchez, Rocío Rivera-Egea, et al.Andrology|June 26, 2022
Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertilityMiriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jiménez, et al.Andrology|March 30, 2021
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohortMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.Frontiers in Cell and Developmental Biology|January 2, 2023
Contribution of <i>TEX15</i> genetic variants to the risk of developing severe non-obstructive oligozoospermiaAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.Journal of Personalized Medicine|January 1, 2021
Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic ImpairmentMiriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, et al.Pageof 16