Results 201 to 210 of about 119,722 (304)
Abstract figure legend Sodium thiosulfate (STS) rescues the pronephros phenotype of pdx1 morphants through compensatory upregulation of nitric oxide (NO) metabolism. Zebrafish larvae injected with a control morpholino show the typical pronephros structure at 48 h post‐fertilization (hpf) with and without STS treatment.
Hannes Ott +6 more
wiley +1 more source
Methylation-regulated tumor suppressor gene <i>HOXB4</i> inhibits human lung adenocarcinoma A549 cell invasion and metastasis through the RAP1 signaling pathway. [PDF]
Zhang L +5 more
europepmc +1 more source
Caenorhabditis elegans as an in vivo model system for human inherited primary arrhythmia syndromes
Abstract figure legend Most genes involved in inherited primary arrhythmia syndromes (IPAS) are conserved in Caenorhabditis elegans, where genetic manipulation enables functional characterization of variants, identification of regulatory proteins, and in vivo drug testing.
Antoine Delinière +6 more
wiley +1 more source
Homeobox transcription factor BmHox7 is required for sexual reproduction, but not for appressorial development and pathogenicity in <i>Bipolaris maydis</i>. [PDF]
Koya S +5 more
europepmc +1 more source
ABSTRACT Resistance to chemotherapy, which is demonstrated in almost every patient with advanced‐stage lung cancer (ALC), underscores an urgent need to unravel the underlying molecular mechanisms and identify novel strategies to overcome drug resistance. In the present study, an attempt was made to identify epigenetic targets and modulators that can be
Okibur Rahman +2 more
wiley +1 more source
ISX promotes tumor migration and invasion in lung cancer by upregulating COL1A1 <i>in vitro</i>. [PDF]
Ma Y +8 more
europepmc +1 more source
ABSTRACT To investigate the correlation between genetic abnormalities and fetal genitourinary (GU) anomalies in Eastern China and to provide assistance for the clinical management of fetuses with different types of GU anomalies. Five hundred forty‐five fetuses with GU anomalies were enrolled, undergoing karyotyping, copy number variation sequencing ...
Jie Liang +6 more
wiley +1 more source
Epigenome-Wide Search for Distinctive Methylation Biomarkers of Endothelial and Leukocyte DNA. [PDF]
Korolenya VA +2 more
europepmc +1 more source
ABSTRACT Bladder exstrophy and epispadias complex (BEEC) is one of the most severe congenital malformations of the urogenital tract, significantly impacting continence, sexual function, and renal function. To date, the only recurrent genetic aberration identified is the 22q.11.2 microduplication, but several candidate regions and genes including ...
Agneta Nordenskjöld +9 more
wiley +1 more source
Lf2 is a knotted homeobox regulator that modulates leaflet number in soybean. [PDF]
Clark CB +9 more
europepmc +1 more source

