Results 231 to 240 of about 596,095 (346)

Loss of Golga7 Suppresses Oncogenic Nras‐Driven Leukemogenesis without Detectable Toxicity in Adult Mice

open access: yesAdvanced Science, EarlyView.
NRAS mutations are widespread in hematologic malignancies. Our study shows that GOLGA7 serves as a safe and effective therapeutic target for NRAS‐driven leukemia. Loss of Golga7 in adult mice effectively suppresses NrasG12D‐driven myeloproliferative neoplasm by disrupting its PM localization and impairing subsequent MAPK signaling, without affecting ...
Bo Jiao   +18 more
wiley   +1 more source

New strategy for Pinus pinaster genomic library construction in bacterial artificial chromosomes

open access: diamond, 2008
Rocí­o Bautista   +5 more
openalex   +2 more sources

Expression of heterologous sigma factors enables functional screening of metagenomic and heterologous genomic libraries [PDF]

open access: gold, 2015
Stefan M. Gaida   +5 more
openalex   +1 more source

Leveraging Automated Machine Learning for Environmental Data‐Driven Genetic Analysis and Genomic Prediction in Maize Hybrids

open access: yesAdvanced Science, EarlyView.
An automated machine learning framework integrating environmental and genomic data enhances genetic analysis and genomic prediction in maize. By leveraging dimension‐reduced environmental parameters, it reveals trait‐environment relationships and identifies genetic markers that govern phenotypic plasticity and genotype‐by‐environment interactions.
Kunhui He   +12 more
wiley   +1 more source

Polygenic Inheritance for Common Comorbidities Associated With Congenital Heart Disease. [PDF]

open access: yesJACC Adv
Thompson JM   +9 more
europepmc   +1 more source

Generation of a pooled shRNA library for functional genomics screens

open access: gold, 2022
Dimitrios Papadopoulos   +2 more
openalex   +1 more source

DPImpute: A Genotype Imputation Framework for Ultra‐Low Coverage Whole‐Genome Sequencing and its Application in Genomic Selection

open access: yesAdvanced Science, EarlyView.
DPImpute is a two‐step pipeline that outperforms existing tools in whole‐genome SNP imputation, particularly under conditions of ultra‐low coverage sequencing, small sample sizes, and limited references. It enables precise imputation for single blastocyst cells, supporting genomic selection at the pre‐implantation stage.
Weigang Zheng   +11 more
wiley   +1 more source

Home - About - Disclaimer - Privacy