Results 111 to 120 of about 30,580 (249)
Meiotic recombination and male infertility: from basic science to clinical reality? [PDF]
Infertility is a common problem that affects approximately 15% of the population. Although many advances have been made in the treatment of infertility, the molecular and genetic causes of male infertility remain largely elusive. This review will present
Hann, Michael C. +2 more
core +1 more source
ABSTRACT Background Cell therapy, particularly those utilizing mesenchymal stem/stromal cells (MSCs), is gaining traction as a therapeutic option for regenerative treatment in patients with limited therapeutic options. Although the safety of MSC‐based interventions is well established, uncertainties remain regarding how genetic abnormalities and ...
Marzena Zychowicz +12 more
wiley +1 more source
Altered cohesin gene dosage affects Mammalian meiotic chromosome structure and behavior.
Based on studies in mice and humans, cohesin loss from chromosomes during the period of protracted meiotic arrest appears to play a major role in chromosome segregation errors during female meiosis.
Brenda Murdoch +11 more
doaj +1 more source
Analysis of small RNAs revealed differential expressions during pollen and embryo sac development in autotetraploid rice [PDF]
Protein-protein interaction of meiosis-related genes with the targets predicted by the DEM associated with meiosis. Table S18. 21 nt-phasiRNAs triggered by the miR2118. Table S19. 24 nt-phasiRNAs triggered by the miR2275. Table S20. Overview of 24 nt TEs-
Jinwen Wu +8 more
core +5 more sources
ABSTRACT Introduction Direct experimental investigation of Klinefelter syndrome (KS) in patients is limited because the syndrome manifests heterogeneously and affects multiple organ systems. Studying KS therefore requires a model that captures this complexity as accurately as possible while still permitting controlled experimental manipulation ...
Fariba Saadati, Joachim Wistuba
wiley +1 more source
Anàlisi citogenètica d'espermatozoides humans [PDF]
Les anomalies cromosòmiques són una de les principals causes d'esterilitat en l'espècie humana. A les anomalies del cariotip, molt més freqüents en individus que consulten per problemes reproductius que en la població general, s'afegeixen les anomalies ...
Anton, Ester +3 more
core
Summary Germline gain‐of‐function variants in sterile alpha motif domain–containing 9‐like (SAMD9L), located on chromosome 7q, cause a multisystem disorder characterized by bone marrow failure, immunodeficiency and variable neurological involvement. Disease evolution is frequently shaped by somatic genetic rescue (SGR), most commonly through monosomy 7,
Hadjer Dellal +10 more
wiley +1 more source
Exposure of Tradescantia Microspores to Periodic Vibrations of 40-100 Hertz [PDF]
Spherical chromosomal fragments determined in exposure of Tradescantia microspores to periodic ...
Bales, L. J., Knepton, J. C., Jr.
core +1 more source
Analysis of Human Uniparental Embryonic Stem Cells Reveals New Putative Imprinted Loci
To identify novel imprinted genes, parthenogenetic, androgenetic and biparental human embryonic stem cells and their differentiated neural progenitors were analysed by methylome and transcriptome profiling. This approach uncovered 12 putative novel imprinted genes, including a clustered region on chromosome 19, expanding the current catalogue of ...
Shay Kinreich, Nissim Benvenisty
wiley +1 more source
Anthropogenic Impacts on Meiosis in Plants
As the human population grows and continues to encroach on the natural environment, organisms that form part of such ecosystems are becoming increasingly exposed to exogenous anthropogenic factors capable of changing their meiotic landscape.
Lorenz K. Fuchs +2 more
doaj +1 more source

