Results 241 to 250 of about 55,016 (311)

Limited Clinical Impact of Androgen Receptor Repeat Length (CAG and GGC) in Klinefelter Syndrome: A Multivariable Analysis

Andrology, EarlyView.
ABSTRACT Background Klinefelter syndrome (KS) is characterized by marked phenotypic heterogeneity that might be influenced by genetic modifiers, including androgen receptor (AR) repeat length (CAGn and GGCn). The clinical relevance of these repeat lengths in patients with KS before testosterone replacement therapy (TRT) remains unclear.
Andrea Graziani, Alberto Scala, Maria Santa Rocca, Cinzia Vinanzi, Giuseppe Grande, Andrea Di Nisio, Riccardo Selice, Antonella Di Mambro, Alberto Ferlin   +8 more
wiley   +1 more source

Mouse germline cysts contain a fusome-like structure that mediates oocyte development. [PDF]

Elife
Pathak M, Spradling AC.
europepmc   +1 more source

A Spotlight on Yolk‐sac Tumors: Molecular Pathology, Current Diagnostics, and Novel Therapeutics

Andrology, EarlyView.
ABSTRACT Background Yolk‐sac tumors are an aggressive subtype of testicular cancer that significantly contribute to disease progression and therapy resistance, especially in adults. While testicular cancer generally has high cure rates with cisplatin‐based treatment, adult yolk‐sac tumors often appear as components of mixed tumors with poor response to
Evangelos Prokakis, Lisa Schneider, Felix Bremmer, Daniel Nettersheim   +3 more
wiley   +1 more source

Wt1 Is Required for the Regression of Müllerian Ducts in Male Mice by Inducing Wif1 and Osx Expression. [PDF]

Cell Prolif
Chen M, Qi X, Qin S, Kang J, Cen C, Guo M, Gao Y, Wang M, Li J, Cui X, Wang Y, Zhu L, Gao F.   +12 more
europepmc   +1 more source

Sleep Disorders in Klinefelter Syndrome and Other Sex Chromosome Aneuploidies: A Narrative Review

Andrology, EarlyView.
ABSTRACT Background Sex chromosome aneuploidies (SCAs) are among the most frequent types of chromosomal aneuploidies and include Klinefelter syndrome (47,XXY and higher‐grade variants), 47,XYY syndrome, Turner syndrome (45,X), and trisomy X (47,XXX).
Roberto Paparella, Fabiola Panvino, Ida Pucarelli, Luigi Tarani   +3 more
wiley   +1 more source

Double Torsion of a Continuous Type of a Splenogonadal Fusion Presenting as an Inguinoscrotal Emergency: A Rare Case Report. [PDF]

Int Med Case Rep J
Ahmad O, Shbani A, Ranjous Y, Alkhabbaz O, Khabbaz AAM.   +4 more
europepmc   +1 more source

Kinetic analysis of strand invasion intermediates during C. elegans meiosis reveals continuous sister- and homolog-directed repair. [PDF]

Genetics
Hamrick A, Cope HD, Forbis D, Rog O.
europepmc   +1 more source

Optimal male fertility and fecundity in Caenorhabditis elegans require Microprocessor and Argonaute gene function. [PDF]

G3 (Bethesda)
Lu L, Rios C, Abbott AL.
europepmc   +1 more source

Regulation of hlh-2 transcription during specification of the anchor cell of the C. elegans hermaphrodite gonad. [PDF]

G3 (Bethesda)
Kim JH, Greenwald I.
europepmc   +1 more source

Two adult 46,XY sisters with female-like phenotype due to a novel homozygous <i>LHCGR</i> splice-site variant. [PDF]

JCEM Case Rep
Meirelles MG, Scalco RC, Marques JM, Lima Junior J, Bueno CF, Mendonca BB.   +5 more
europepmc   +1 more source