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Items: 1 to 20 of 101

1.

Gynogenetic activation of porcine oocytes.

Lee K, Wang C, Spate L, Murphy CN, Prather RS, Machaty Z.

Cell Reprogram. 2014 Apr;16(2):121-9. doi: 10.1089/cell.2013.0074.

PMID:
24661186
2.

Analysis of cat oocyte activation methods for the generation of feline disease models by nuclear transfer.

Wang C, Swanson WF, Herrick JR, Lee K, Machaty Z.

Reprod Biol Endocrinol. 2009 Dec 11;7:148. doi: 10.1186/1477-7827-7-148.

4.

Effect of cytochalasins B and D on the developmental competence of somatic cell nuclear transfer embryos in miniature pigs.

Sugimura S, Kawahara M, Wakai T, Yamanaka K, Sasada H, Sato E.

Zygote. 2008 May;16(2):153-9. doi: 10.1017/S0967199407004480.

PMID:
18405436
6.

Involvement of calcium signaling and the actin cytoskeleton in the membrane block to polyspermy in mouse eggs.

McAvey BA, Wortzman GB, Williams CJ, Evans JP.

Biol Reprod. 2002 Oct;67(4):1342-52.

PMID:
12297554
7.

Paternal influence of sperm DNA integrity on early embryonic development.

Simon L, Murphy K, Shamsi MB, Liu L, Emery B, Aston KI, Hotaling J, Carrell DT.

Hum Reprod. 2014 Nov;29(11):2402-12. doi: 10.1093/humrep/deu228.

PMID:
25205757
8.

Effect of actin polymerization inhibitor during oocyte maturation on parthenogenetic embryo development and ploidy in Capra hircus.

Ranjan R, Singh RK, Yasotha T, Kumar M, Puri G, Kumar K, Singh R, Bhure S, Malakar D, Bhanja SK, Sarkar M, Das BC, Bag S.

Biochem Genet. 2013 Dec;51(11-12):944-53. doi: 10.1007/s10528-013-9619-4.

PMID:
23846112
9.

Diploid porcine parthenotes produced by inhibition of first polar body extrusion during in vitro maturation of follicular oocytes.

Somfai T, Ozawa M, Noguchi J, Kaneko H, Ohnuma K, Karja NW, Fahrudin M, Maedomari N, Dinnyés A, Nagai T, Kikuchi K.

Reproduction. 2006 Oct;132(4):559-70.

10.
11.

Chromosomes in the porcine first polar body possess competence of second meiotic division within enucleated MII stage oocytes.

Lin T, Diao YF, Kang JW, Lee JE, Kim DK, Jin DI.

PLoS One. 2013 Dec 3;8(12):e82766. doi: 10.1371/journal.pone.0082766.

12.

Centrosomal protein centrin is not detectable during early pre-implantation development but reappears during late blastocyst stage in porcine embryos.

Manandhar G, Feng D, Yi YJ, Lai L, Letko J, Laurincik J, Sutovsky M, Salisbury JL, Prather RS, Schatten H, Sutovsky P.

Reproduction. 2006 Sep;132(3):423-34.

13.

The Principal Forces of Oocyte Polarity Are Evolutionary Conserved but May Not Affect the Contribution of the First Two Blastomeres to the Blastocyst Development in Mammals.

Hosseini SM, Moulavi F, Tanhaie-Vash N, Asgari V, Ghanaei HR, Abedi-Dorche M, Jafarzadeh N, Gourabi H, Shahverdi AH, Dizaj AV, Shirazi A, Nasr-Esfahani MH.

PLoS One. 2016 Mar 31;11(3):e0148382. doi: 10.1371/journal.pone.0148382.

14.
16.

Activation with ionomycin followed by dehydroleucodine and cytochalasin B for the production of parthenogenetic and cloned bovine embryos.

Canel N, Bevacqua R, Fernández-Martín R, Salamone DF.

Cell Reprogram. 2010 Aug;12(4):491-9. doi: 10.1089/cell.2009.0109.

PMID:
20698787
17.

A simple method for producing tetraploid porcine parthenogenetic embryos.

Sembon S, Fuchimoto D, Iwamoto M, Suzuki S, Yoshioka K, Onishi A.

Theriogenology. 2011 Sep 1;76(4):598-606. doi: 10.1016/j.theriogenology.2011.03.010.

PMID:
21652062
18.

Expression of mitochondrial transcription factor A (TFAM) during porcine gametogenesis and preimplantation embryo development.

Antelman J, Manandhar G, Yi YJ, Li R, Whitworth KM, Sutovsky M, Agca C, Prather RS, Sutovsky P.

J Cell Physiol. 2008 Nov;217(2):529-43. doi: 10.1002/jcp.21528.

PMID:
18636550
20.

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