Results 31 to 40 of about 10,363 (245)
The Euler-Minding series for branched continued fractions
For suitable x(k) (k\(\geq 1)\) and y(k) (k\(\geq 0)\) denote the continued fraction \(y(0)+x(1)/y(1)+...x(j)/y(j)\) by \(K\{\) x(k),y(k);j\(\}\). With twin sequences a(i,k) (k\(\geq 1)\) and b(i,k) (k\(\geq 0)\) prescribed for \(i\geq 0\), let \(C(i,j)=K\{a(i,k),b(i,k);j\}\).
openaire +3 more sources
Embryo‐like structures (stembryos) are an innovative tool, but they are hindered by experimental variability and limited developmental potential. DNA methylation is crucial for mammalian development, but its status in stembryo models is poorly characterized.
Sara Canil +4 more
wiley +1 more source
Tumour–host interactions in Drosophila: mechanisms in the tumour micro‐ and macroenvironment
This review examines how tumour–host crosstalk takes place at multiple levels of biological organisation, from local cell competition and immune crosstalk to organism‐wide metabolic and physiological collapse. Here, we integrate findings from Drosophila melanogaster studies that reveal conserved mechanisms through which tumours hijack host systems to ...
José Teles‐Reis, Tor Erik Rusten
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Три- і чотиричленні рекурентні співвідношення для гіпергеометричної функції Горна $$$H_4$$$
Three- and four-term recurrence relations for hypergeometric functions of the second order (such as hypergeometric functions of Appell, Horn, etc.) are the starting point for constructing branched continued fraction expansions of the ratios of these ...
I.-A.V. Lutsiv +3 more
core +1 more source
We analyze cisplatin–DNA adducts (CDAs) and double‐strand breaks (DSBs) in a cell‐cycle‐dependent manner. We find that CDAs form similarly across all cell cycle phases. DSBs arise only in S‐phase. CDAs might not directly impair DSB repair, but S‐phase DSB lesions evolve in the presence of CDAs and disrupt repair in G2, also causing radiosensitization ...
Ye Qiu +10 more
wiley +1 more source
Convergence criteria of branched continued fractions
The convergence criteria of branched continued fractions with N branches of branching and branched continued fractions of the special form are analyzed. The classical theorems of convergence of continued fractions that have become the subject of multidimensional generalizations are formulated.
I.B. Bilanyk, D.I. Bodnar, O.G. Vozniak
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Nuclear pore links Fob1‐dependent rDNA damage relocation to lifespan control
Damaged rDNA accumulates at a specific perinuclear interface that couples nucleolar escape with nuclear envelope association. Nuclear pores at this site help inhibit Fob1‐induced rDNA instability. This spatial organization of damage handling supports a functional link between nuclear architecture, rDNA stability, and replicative lifespan in yeast.
Yamato Okada +5 more
wiley +1 more source
Truncation error bounds for branched continued fractions of the special form are established. These fractions can be obtained by fixing the values of variables in branched continued fractions with independent variables, which is an effective tool for ...
Bodnar, D.I. +2 more
core +1 more source
In a murine model of myocardial ischemia and reperfusion (MI/R), the CD36 azapeptide ligand MPE‐298 reduces cardiac injury and transiently lowers left ventricular long‐chain fatty acids (LCFAs) accumulation 3 h after reperfusion, accompanied by a decrease of oxidative stress and inflammation‐associated genes' expression in the heart and adipose tissue.
Jade Gauvin +12 more
wiley +1 more source
Aging Is a Key Driver for Adult Acute Myeloid Leukemia
Acute myeloid leukemia (AML) is a classical age‐related hematologic malignancy, and a key driver of AML is aging, which profoundly regulates intrinsic factors such as genomic instability, epigenetic reprogramming, and metabolic dysregulation, and alters bone marrow microenvironment.
Rong Yin, Haojian Zhang
wiley +1 more source

