Results 181 to 190 of about 67,099 (264)

Transcriptional Profiling at Single‐Cell Resolution Reveals Diversity and Regulatory Networks of Primary and Secondary Senescent Cells

open access: yesAging Cell, Volume 25, Issue 5, May 2026.
The research article “Transcriptional Profiling at Single‐cell Resolution Reveals Diversity and Regulatory Networks of Primary and Secondary Senescent Cells” by Jang, Shim, et al. models primary senescence by X‐ray irradiation and secondary senescence by conditioned media transfer in human renal epithelial cells. Single‐cell RNA‐seq identifies distinct
Dong‐Hyun Jang   +8 more
wiley   +1 more source

Non-Canonical Male Meiosis in a Marine Gastropod, <i>Littorina saxatilis</i>. [PDF]

open access: yesBiology (Basel)
Demin SI   +3 more
europepmc   +1 more source

Spastin is an essential regulator of male meiosis, acrosome formation, manchette structure and nuclear integrity.

open access: yesDevelopment, 2023
Cheers SR   +5 more
europepmc   +1 more source

Pharmacogenetics of follicle‐stimulating hormone action in the male

open access: yesAndrology, Volume 14, Issue 4, Page 1064-1072, May 2026.
Abstract Male factor infertility (MFI) is involved in half of the cases of couple infertility. The follicle‐stimulating hormone (FSH) therapy is considered efficient to improve semen parameters and pregnancy rate in patients with idiopathic MFI, following the lesson learned from hypogonadotropic hypogonadism.
Andrea Graziani   +7 more
wiley   +1 more source

Fetal Fraction Signatures: A Quality Control Tool to Detect Potentially Confounding Situations in NonInvasive Prenatal Diagnosis of Monogenic Conditions

open access: yesClinical Genetics, Volume 109, Issue 5, Page 869-875, May 2026.
Noninvasive prenatal diagnosis for monogenic diseases (NIPD‐M) to detect inherited mutations is performed in parallel with fetal fraction signatures, to detect various anomalies that may compromise diagnosis. An extra regression analysis may be necessary to resolve mosaic situations. ABSTRACT Noninvasive prenatal diagnosis relies on the analysis of the
Jean‐Louis Blouin   +2 more
wiley   +1 more source

SMARCA5 restricts chromatin accessibility to promote male meiosis and fertility in mammals. [PDF]

open access: yesProc Natl Acad Sci U S A
Kataruka S   +6 more
europepmc   +1 more source

Mutation in MSH5 Causes Primary Ovarian Insufficiency and Successful Therapeutic Intervention by In Vitro Fertilisation

open access: yesJournal of Cellular and Molecular Medicine, Volume 30, Issue 9, May 2026.
ABSTRACT Primary ovarian insufficiency (POI) is a genetically heterogeneous disorder characterised by cessation of menstruation before the age of 40 years with elevated levels of follicle‐stimulating hormone. Germline variants in the MSH5 gene cause POI. In this study, we investigated a Han Chinese family with POI.
Bin Mao   +9 more
wiley   +1 more source

Male meiosis in structural heterozygotes

open access: yes
ABSTRACT The incident of structural heterozygosity is presently noticed for the first time in 9 diploid species, namely, Artemisia annua (n=9), Datura stramonium (n=12), Dicliptera bupleuroides (n=13), Hemigraphis latebrosa (n=12), Leycesteria formosa (n=9), Salvia plebeia (n=8), Senecio nudicaulis (n=5), Sonchus brachyotus (n=9) and Verbena ...
openaire   +1 more source

Plastid and nuclear phylogenomics of Cyphostemma (Vitaceae) provide new insights into genome size evolution across sub‐Saharan Africa

open access: yesJournal of Integrative Plant Biology, Volume 68, Issue 5, Page 1399-1420, May 2026.
Some African Cyphostemma species evolved much larger genomes as they adapted to dry, rocky habitats. These expansions are linked to succulent traits and specialization on nutrient‐rich limestone outcrops. The findings show how climate‐driven aridification shaped plant evolution and highlight broader genome‐environment patterns across flowering plants ...
Rindra M. Ranaivoson   +18 more
wiley   +1 more source

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