Results 311 to 320 of about 6,270,911 (362)

X‑chromosome loss rescues Sertoli cell maturation and spermatogenesis in Klinefelter syndrome. [PDF]

Cell Death Dis
Winge SB, Skakkebaek NE, Aksglaede L, Saritaş G, Rajpert-De Meyts E, Goossens E, Juul A, Almstrup K.   +7 more
europepmc   +1 more source

Genetic parameters and genome-wide association studies including the X chromosome for various reproduction and semen quality traits in Nellore cattle. [PDF]

BMC Genomics
de Carvalho FE, Ferraz JBS, Pedrosa VB, Matos EC, Eler JP, Silva MR, Guimarães JD, Bussiman F, Silva BCA, Mulim HA, Rocha AO, Araujo AC, Wen H, Campos GS, Brito LF.   +14 more
europepmc   +1 more source

The interferon γ pathway enhances pluripotency and X-chromosome reactivation in iPSC reprogramming. [PDF]

Sci Adv
Barrero M, Lazarenkov A, Blanco E, Palma LG, López-Rubio AV, Bauer M, Bigas A, Di Croce L, Sardina JL, Payer B.   +9 more
europepmc   +1 more source

Synergistic Effects of Extra X Chromosome on Development of Systemic Lupus Erythematosus and Sjögren Disease in Klinefelter and Triple X Syndrome: A Retrospective Cohort Study. [PDF]

ACR Open Rheumatol
Palmer AK, Tan IJ.
europepmc   +1 more source

X chromosome dosage drives statin-induced dysglycemia and mitochondrial dysfunction. [PDF]

Nat Commun
Zhang P, Munier JJ, Wiese CB, Vergnes L, Link JC, Abbasi F, Ronquillo E, Scheker K, Muñoz A, Kuang YL, Theusch E, Lu M, Sanchez G, Oni-Orisan A, Iribarren C, McPhaul MJ, Nomura DK, Knowles JW, Krauss RM, Medina MW, Reue K.   +20 more
europepmc   +1 more source

Maternal X chromosome pericentric inversion resulting in the genetic analysis of offspring pedigrees with deletions at Xp22.33 and Xp22.33p11.3, and duplications at Xq27.3q28: Case report. [PDF]

Medicine (Baltimore)
Deng GS, Lai YQ, Luo BW, Luo YD, Zhu LL, Yang ZY, Feng K, Li DR, Li X.   +8 more
europepmc   +1 more source

Inferring clonal somatic mutations directed by X chromosome inactivation status in single cells. [PDF]

Genome Biol
Demirci I, Larsson AJM, Chen X, Hartman J, Sandberg R, Frisén J.   +5 more
europepmc   +1 more source

Cdk8 and Hira mutations trigger X chromosome elimination in naive female hybrid mouse embryonic stem cells. [PDF]

Chromosome Res
Halter K, Chen J, Priklopil T, Monfort A, Wutz A.   +4 more
europepmc   +1 more source