Results 211 to 220 of about 6,791 (285)

Pirfenidone Reverts Global DNA Hypomethylation, Promoting DNMT1/UHRF/PCNA Coupling Complex in Experimental Hepatocarcinoma. [PDF]

open access: yesCells
Miranda-Roblero HO   +11 more
europepmc   +1 more source

Perfil dos Egressos dos Cursos do Instituto Nacional de Câncer José Alencar Gomes da Silva: Pós-Graduação Lato Sensu e Nível Técnico

open access: diamond, 2013
Luiz Cláudio Santos Thuler   +4 more
openalex   +2 more sources

Tumor banking for health research in Brazil and Latin America: time to leave the cradle [PDF]

open access: yes, 2017
Antonio Hugo Jose Froes Marques Campos   +2 more
core   +1 more source

Perspectives on the Current and Future State of Artificial Intelligence in Medical Genetics

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Artificial intelligence (AI) is rapidly transforming numerous aspects of daily life, including clinical practice and biomedical research. In light of this rapid transformation, and in the context of medical genetics, we assembled a group of leaders in the field to respond to the question about how AI is affecting, and especially how AI will ...
Benjamin D. Solomon   +20 more
wiley   +1 more source

[Community activities carried out in Primary Care in Galicia between 2018 and 2022: A descriptive study]. [PDF]

open access: yesAten Primaria
Mosteiro-Miguéns DG   +5 more
europepmc   +1 more source

MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study. [PDF]

open access: yesJ Assist Reprod Genet, 2022
Silva LR   +8 more
europepmc   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong   +16 more
wiley   +1 more source

New Advances in the Study of CMTM6, a Focus on Its Novel Non-Canonical Cellular Locations, and Functions beyond Its Role as a PD-L1 Stabilizer. [PDF]

open access: yesCancers (Basel)
Urciaga-Gutierrez PI   +14 more
europepmc   +1 more source

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