1
|
Ye Y, Li N, Yan X, Wu R, Zhou W, Cheng L
and Li Y: Genetic analysis of embryo in a human case of spontaneous
oocyte activation: A case report. Gynecol Endocrinol. 36:294–296.
2020.PubMed/NCBI View Article : Google Scholar
|
2
|
Combelles CM, Kearns WG, Fox JH and
Racowsky C: Cellular and genetic analysis of oocytes and embryos in
a human case of spontaneous oocyte activation. Hum Reprod.
26:545–552. 2011.PubMed/NCBI View Article : Google Scholar
|
3
|
Oliveira FG, Dozortsev D, Diamond MP,
Fracasso A, Abdelmassih S, Abdelmassih V, Gonçalves SP, Abdelmassih
R and Nagy ZP: Evidence of parthenogenetic origin of ovarian
teratoma: Case report. Hum Reprod. 19:1867–1870. 2004.PubMed/NCBI View Article : Google Scholar
|
4
|
Socolov R, Ebner T, Gorduza V, Martiniuc
V, Angioni S and Socolov D: Self-oocyte activation and
parthenogenesis: An unusual outcome of a misconducted IVF cycle.
Gynecol Endocrinol. 31:529–530. 2015.PubMed/NCBI View Article : Google Scholar
|
5
|
Jiang Y, Cao Q, Zhao X, Li L, Li S and Gao
F: Percutaneous epididymal sperm aspiration and short time
insemination in the treatment of men with obstructive azoospermia.
J Assist Reprod Genet. 30:1175–1179. 2013.PubMed/NCBI View Article : Google Scholar
|
6
|
Jiang Y, Song G, Yuan J and Zhang X: ICSI
with all oocytes recurrent Metaphase I characterized by absence
perivitelline space. Open J Obstet Gynecol. 11:1112–1116. 2021.
|
7
|
McGowan-Jordan J, Ros JH and Sarah M
(eds): ISCN 2020: An international system for human cytogenomic
nomenclature. 1st edition. S. Karger AG, Basel, pp341-503,
2020.
|
8
|
Bonte D, Ferrer-Buitrago M, Dhaenens L,
Popovic M, Thys V, De Croo I, De Gheselle S, Steyaert N, Boel A,
Vanden Meerschaut F, et al: Assisted oocyte activation
significantly increases fertilization and pregnancy outcome in
patients with low and total failed fertilization after
intracytoplasmic sperm injection: A 17-year retrospective study.
Fertil Steril. 112:266–274. 2019.PubMed/NCBI View Article : Google Scholar
|
9
|
Ducibella T, Huneau D, Angelichio E, Xu Z,
Schultz RM, Kopf GS, Fissore R, Madoux S and Ozil JP: Egg-to-embryo
transition is driven by differential responses to Ca(2+)
oscillation number. Dev Biol. 250:280–291. 2002.PubMed/NCBI
|
10
|
Paffoni A, Paracchini V, Ferrari S,
Scarduelli C, Seia M, Coviello DA and Ragni G: Use of
parthenogenetic activation of human oocytes as an experimental
model for evaluation of polar body based PGD assay performance. J
Assist Reprod Genet. 28:461–470. 2011.PubMed/NCBI View Article : Google Scholar
|
11
|
Kaufman MH: Parthenogenetic activation of
Oocytes. Cold Spring Harb Protoc. 2018:20–23. 2018.PubMed/NCBI View Article : Google Scholar
|
12
|
Yamazawa K, Nakabayashi K, Kagami M, Sato
T, Saitoh S, Horikawa R, Hizuka N and Ogata T: Parthenogenetic
chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype.
J Med Genet. 47:782–785. 2010.PubMed/NCBI View Article : Google Scholar
|
13
|
Kaneda M, Takahashi M, Yamanaka KI, Saito
K, Taniguchi M, Akagi S, Watanabe S and Nagai T: Epigenetic
analysis of bovine parthenogenetic embryonic fibroblasts. J Reprod
Dev. 63:365–375. 2017.PubMed/NCBI View Article : Google Scholar
|
14
|
Winston N, Johnson M, Pickering S and
Braude P: Parthenogenetic activation and development of fresh and
aged human oocytes. Fertil Steril. 56:904–912. 1991.PubMed/NCBI
|
15
|
Conlin LK, Thiel BD, Bonnemann CG, Medne
L, Ernst LM, Zackai EH, Deardorff MA, Krantz ID, Hakonarson H and
Spinner NB: Mechanisms of mosaicism, chimerism and uniparental
disomy identified by single nucleotide polymorphism array analysis.
Hum Mol Genet. 19:1263–1275. 2010.PubMed/NCBI View Article : Google Scholar
|
16
|
Yamazawa K, Ogata T and Ferguson-Smith AC:
Uniparental disomy and human disease: An overview. Am J Med Genet C
Semin Med Genet. 154C:329–334. 2010.PubMed/NCBI View Article : Google Scholar
|
17
|
Gueye NA, Devkota B, Taylor D, Pfundt R,
Scott RT Jr and Treff NR: Uniparental disomy in the human
blastocyst is exceedingly rare. Fertil Steril. 101:232–236.
2014.PubMed/NCBI View Article : Google Scholar
|
18
|
Liehr T: Formation of UPD. In: Uniparental
Disomy (UPD) in Clinical Genetics. Springer, Berlin, Heidelberg,
2014.
|
19
|
Nikitina TV and Nazarenko SA: Mutation in
microsatellite repeats of DNA and embryonal death in humans.
Genetika. 36:965–971. 2000.PubMed/NCBI
|
20
|
Masset H, Tšuiko O and Vermeesch JR:
Genome-wide abnormalities in embryos: Origins and clinical
consequences. Prenat Diagn. 41:554–563. 2021.PubMed/NCBI View
Article : Google Scholar
|