Results 121 to 130 of about 409,247 (302)
LOSS OF A PORTION of the long arm of chromosome 5 is seen predominantly in therapy-related myelodysplastic syndromes and acute leukemias, as well as in a unique clinical disorder known as the 5q– syndrome.
Nimer, Stephen D, Golde, David W
core +1 more source
Chromosomal abnormalities and « hypoprolificacy » [PDF]
Popescu, P., Legault, C.
openaire +2 more sources
In TP53mut GBM cells, reduced P53 function is associated with increased TET1 expression. Genetic or pharmacological inhibition of TET1 correlates with genome fragility, including DNA damage, cellular senescence, telomere shortening, and reactive oxygen species accumulation, which may contribute to increased efficacy of antitumor therapy.
Zhuonan Pu +12 more
wiley +1 more source
A cytokinin pathway transcription factor, RR2b, was artificially selected during soybean domestication and improvement based on its differential transcriptional activity, which correlates with ATT repeat polymorphisms in its promoter. RR2b balances yield and defense by fine‐tuning its expression level and offers a promising target for decoupling trade ...
Qun Ma +11 more
wiley +1 more source
Chromosomal Abnormalities in Lymphoma [PDF]
A S, SPIERS, A G, BAIKIE
openaire +2 more sources
NSD2 coordinates the neurogenic‐to‐gliogenic transition in the developing neocortex through H3K36me2‐dependent activation of EGFR–ERK signaling. Loss of NSD2 disrupts astroglial and oligodendroglial development, whereas ERK activation rescues gliogenic defects in vitro and in vivo.
Hanxue Chen +7 more
wiley +1 more source
This study unveils a novel antibacterial mechanism against MRSA, in which the compound Py‐27 selectively targets and inhibits aspartate transcarbamoylase (ATCase), a key enzyme in pyrimidine synthesis. This inhibition disrupts DNA replication, induces oxidative damage, leading to potent bactericidal activity.
Xiaorong Yang +11 more
wiley +1 more source
Structural Chromosome Abnormality in Recurrent Pregnancy Loss in Gaza Strip: First Experience [PDF]
Objective This study was conducted in order to evaluate the type and frequency of structural chromosome abnormality in phenotypically normal couples suffering from recurrent pregnancy loss.
Sharif, Fadel A.
core
MicroRNA-146b overexpression associates with deteriorated clinical characteristics, increased International Staging System stage, cacoethic chromosome abnormality, and unfavorable prognosis in multiple myeloma patients. [PDF]
Bao Y, Wei M, Ji X.
europepmc +1 more source

