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The ISME Journal|April 18, 2025
Heat-induced stress modulates cell surface glycans and membrane lipids of coral symbiontsGiada Tortorelli, Sabrina L Rosset, Clarisse E S Sullivan, et al.
Pharmaceutical Biology|September 27, 2014
Chemical composition and evaluation of acute toxicological, antimicrobial and modulatory resistance of the extract of Murraya paniculataIrwin R A Menezes, Temístocles I Santana, Victor J C Varela, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|July 27, 2022
Socio-epidemiological factors and comorbidities associated with Chagas disease manifestations in two urban reference health care centres in Rio de Janeiro, BrazilLuciana F Portela, Maíra B Mesquita, Juliana M Giraldes, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosomeAde Nubia Xavier Pacanaro, Denise Maria Christofolini, Leslie Domenici Kulikowski, et al.
American Journal of Respiratory Cell and Molecular Biology|January 11, 2020
Functional Impact of Human Genetic Variants of COL18A1/Endostatin on Pulmonary EndotheliumAlice M Goyanes, Aigul Moldobaeva, Mery Marimoutou, et al.
Blood Advances|September 30, 2024
OUTREACH: phase 2 study of lisocabtagene maraleucel as outpatient or inpatient treatment at community sites for R/R LBCLYuliya Linhares, Cesar O Freytes, Mohamad Cherry, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 7, 2023
Developmental impairment in children exposed during pregnancy to maternal SARS-COV2: A Brazilian cohort studyCarolina A D Santos, Artemis P Paula, Gentil G Fonseca Filho, et al.
Clinical Endocrinology|December 7, 2000
Comparison of octreotide acetate LAR and lanreotide SR in patients with acromegalyP Chanson, V Boerlin, C Ajzenberg, et al.
American Journal of Medical Genetics. Part A|June 21, 2017
Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twinsFernanda S Jehee, Valdirene T de Oliveira, Juliana Gurgel-Giannetti, et al.
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