Results 41 to 50 of about 883,268 (297)

STEM: a tool for the analysis of short time series gene expression data-6 [PDF]

open access: yes, 2011
Copyright information:Taken from "STEM: a tool for the analysis of short time series gene expression data"BMC Bioinformatics 2006;7():191-191.Published online 5 Apr 2006PMCID:PMC1456994.Copyright © 2006 Ernst and Bar-Joseph; licensee BioMed Central Ltd ...
Jason Ernst (24617)   +1 more
core   +1 more source

Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies

open access: yesCells, 2023
Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disease that causes premature aging symptoms, such as vascular diseases, lipodystrophy, loss of bone mineral density, and alopecia. HGPS is mostly linked to a heterozygous and de novo mutation
Ramona Hartinger   +4 more
doaj   +1 more source

Identification and Expression Analysis of EPSPS and BAR Families in Cotton

open access: yesPlants, 2023
Weeds seriously affect the yield and quality of crops. Because manual weeding is time-consuming and laborious, the use of herbicides becomes an effective way to solve the harm caused by weeds in fields. Both 5-enolpyruvyl shikimate-3-phosphate synthetase
Zhao Li   +12 more
doaj   +1 more source

Nuevo método para la selección rapida de plantas de banano (Musa spp. AAA cv. Grande naine) transformadas con gen bar procedentes de campo, empleando glufosinato de amonio

open access: yesRevista Colombiana de Biotecnología, 2010
Título en inglés: New method for rapid selection of banana (Musa spp. AAA cv. Grande naine) plants with bar gene in the field using ammonium gluphosinate Resumen Los genes marcadores de la selección son ampliamente utilizados para la ...
Rafael Gómez-Kosky   +4 more
doaj   +2 more sources

A web-based pathway enrichment analysis module for the PharMeBINet database

open access: yesGMS Medizinische Informatik, Biometrie und Epidemiologie, 2023
In modern molecular biology, the quantification of proteins, RNA, and DNA is a standard procedure. Resulting in the generation of large data, researchers need appropriate tools for interpretation.
Königs, Cassandra, Dietrich, Theresa
doaj   +1 more source

Expression of a Maize Ubiquitin Gene Promoter-bar Chimeric Gene in Transgenic Rice Plants [PDF]

open access: yesPlant Physiology, 1992
We have constructed a chimeric gene consisting of the promoter, first exon, and first intron of a maize ubiquitin gene (Ubi-1) and the coding sequence of the bar gene from Streptomyces hygroscopicus. This construct was transferred into rice (Oryza sativa L.) protoplasts via electroporation, and 10 plants were regenerated from calli that had been ...
S, Toki   +8 more
openaire   +2 more sources

Genomic Diversity and Clinical Variability in Pediatric Primary Cutaneous Anaplastic Large Cell Lymphoma: A Case Series

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Primary cutaneous anaplastic large cell lymphoma (pcALCL) is a rare pediatric CD30‐positive T‐cell lymphoproliferative disorder with an excellent prognosis, but its genomic drivers are poorly defined. We report three children with skin‐limited disease demonstrating striking molecular heterogeneity, including NPM::ALK, NUP214::FRK, and a novel ...
Shoshana Greenberger   +7 more
wiley   +1 more source

Negative regulation of active zone assembly by a newly identified SR protein kinase. [PDF]

open access: yesPLoS Biology, 2009
Presynaptic, electron-dense, cytoplasmic protrusions such as the T-bar (Drosophila) or ribbon (vertebrates) are believed to facilitate vesicle movement to the active zone (AZ) of synapses throughout the nervous system.
Ervin L Johnson   +2 more
doaj   +1 more source

Sustained Therapeutic Efficacy of Intravenous Plasminogen Concentrate in Pediatric Patients With Type 1 Plasminogen Deficiency: An Analysis of Dosing Parameters and Clinical Outcomes

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Type 1 plasminogen deficiency (PLGD‐1) is an ultra‐rare autosomal recessive disorder caused by variants in the PLG gene and affects approximately 1.6 individuals per million. The condition is characterized by decreased plasminogen levels and impaired function, resulting in fibrin‐rich lesions on mucous membranes throughout the body.
Charles Nakar   +7 more
wiley   +1 more source

AAV8 gene therapy reverses cardiac pathology and prevents early mortality in a mouse model of Friedreich’s ataxia

open access: yesMolecular Therapy: Methods & Clinical Development
Friedreich’s ataxia (FRDA) is an autosomal-recessive disorder primarily attributed to biallelic GAA repeat expansions that reduce expression of the mitochondrial protein frataxin (FXN).
Joshua C. Chang   +18 more
doaj   +1 more source

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