Transcriptomic profile of genes encoding proteins responsible for regulation of cells differentiation and neurogenesis in vivo and in vitro – an oocyte model approach
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Gosden R, Lee B. Portrait of an oocyte: Our obscure origin. J Clin Invest. 2010;120:973–83; DOI:10.1172/JCI41294.GosdenRLeeBPortrait of an oocyte: Our obscure origin20101209738310.1172/JCI41294284605720364095Open DOISearch in Google Scholar
Kranc W, Chachuła A, Bryja A, Ciesiołka S, Budna J, Wojtanowicz-Mark-iewicz K, Sumelka E, Borys S, Antosik P, Bukowska D, Bruska M, Nowicki M, Kempisty B. Selected molecular and physiological aspects of mammalian ovarian granulosa cells in primary culture. Med Weter. 2016;72:723–7; DOI:10.21521/mw.5606.KrancWChachułaABryjaACiesiołkaSBudnaJWojtanowicz-Mark-iewiczKSumelkaEBorysSAntosikPBukowskaDBruskaMNowickiMKempistyBSelected molecular and physiological aspects of mammalian ovarian granulosa cells in primary culture201672723710.21521/mw.5606Open DOISearch in Google Scholar
Yuan YQ, Van Soom A, Leroy JLMR, Dewulf J, Van Zeveren A, De Kruif A, Peelman LJ. Apoptosis in cumulus cells, but not in oocytes, may influence bovine embryonic developmental competence. Theriogenology. 2005;63:2147–63; DOI:10.1016/j.theriogenology.2004.09.054.YuanYQVan SoomALeroyJLMRDewulfJVan ZeverenADe KruifAPeelmanLJApoptosis in cumulus cells, but not in oocytes, may influence bovine embryonic developmental competence20056321476310.1016/j.theriogenology.2004.09.05415826680Open DOISearch in Google Scholar
Russell DL, Gilchrist RB, Brown HM, Thompson JG. Bidirectional communication between cumulus cells and the oocyte: Old hands and new players? Theriogenology. 2016;86:62–8; DOI:10.1016/j. theriogenology.2016.04.019.RussellDLGilchristRBBrownHMThompsonJGBidirectional communication between cumulus cells and the oocyte: Old hands and new players?20168662810.1016/j.theriogenology.2016.04.01927160446Open DOISearch in Google Scholar
Zhai Y, Yao G, Rao F, Wang Y, Song X, Sun F. Excessive nerve growth factor impairs bidirectional communication between the oocyte and cumulus cells resulting in reduced oocyte competence. Reprod Biol Endocrinol. 2018;16:1–11; DOI:10.1186/s12958-018-0349-7.ZhaiYYaoGRaoFWangYSongXSunFExcessive nerve growth factor impairs bidirectional communication between the oocyte and cumulus cells resulting in reduced oocyte competence20181611110.1186/s12958-018-0349-7586977029580253Open DOISearch in Google Scholar
Hoheisel JD. Microarray technology: Beyond transcript profiling and genotype analysis. Nat Rev Genet. 2006;7:200–10; DOI:10.1038/nrg1809.HoheiselJDMicroarray technology: Beyond transcript profiling and genotype analysis200672001010.1038/nrg180916485019Open DOISearch in Google Scholar
Kossowska-Tomaszczuk K, De Geyter C, De Geyter M, Martin I, Holzgreve W, Scherberich A, Zhang H. The multipotency of luteinizing granulosa cells collected from mature ovarian follicles. Stem Cells. 2009;27:210–9; DOI:10.1634/stemcells.2008-0233.Kossowska-TomaszczukKDe GeyterCDe GeyterMMartinIHolzgreveWScherberichAZhangHThe multipotency of luteinizing granulosa cells collected from mature ovarian follicles200927210910.1634/stemcells.2008-023319224509Open DOISearch in Google Scholar
Shimada M. Cumulus Oocyte Complex: Cumulus Cells Regulate Oocyte Growth and Maturation. J Mamm Ova Res. 2009;26:189–94; DOI:10.1274/jmor.26.189.ShimadaMCumulus Oocyte Complex: Cumulus Cells Regulate Oocyte Growth and Maturation2009261899410.1274/jmor.26.189Open DOISearch in Google Scholar
Chermuła B, Brazert M, Jeseta M, Ożegowska K, Sujka-Kordowska P, Konwerska A, Bryja A, Kranc W, Jankowski M, Nawrocki MJ, Kocherova I, Celichowski P, Borowiec B, Popis M, Budna-Tukan J, Antosik P, Bukowska D, Brussow KP, Pawelczyk L, Bruska M, Zabel M, Nowicki M, Kempisty B. The unique mechanisms of cellular proliferation, migration and apoptosis are regulated through oocyte maturational development—A complete transcriptomic and histochemical study. Int J Mol Sci. 2019;20; DOI:10.3390/ijms20010084.ChermułaBBrazertMJesetaMOżegowskaKSujka-KordowskaPKonwerskaABryjaAKrancWJankowskiMNawrockiMJKocherovaICelichowskiPBorowiecBPopisMBudna-TukanJAntosikPBukowskaDBrussowKPPawelczykLBruskaMZabelMNowickiMKempistyBThe unique mechanisms of cellular proliferation, migration and apoptosis are regulated through oocyte maturational development—A complete transcriptomic and histochemical study20192010.3390/ijms20010084633754830587792Open DOISearch in Google Scholar
Rybska M, Knap S, Jankowski M, Jeseta M, Bukowska D, Antosik P, Nowicki M, Zabel M, Kempisty B, Jaśkowski JM. Characteristic of factors influencing the proper course of folliculogenesis in mammals. Med J Cell Biol. 2018;6:33–8; DOI:10.2478/acb-2018-0006.RybskaMKnapSJankowskiMJesetaMBukowskaDAntosikPNowickiMZabelMKempistyBJaśkowskiJMCharacteristic of factors influencing the proper course of folliculogenesis in mammals2018633810.2478/acb-2018-0006Open DOISearch in Google Scholar
Moncrieff L, Mozdziak P, Jeseta M, Machatkova M, Kranc W, Kempisty B. Ovarian follicular cells - Living in the shadow of stemness cellular competence. Med J Cell Biol. 2019;7:134–40; DOI:10.2478/acb-2019-0018.MoncrieffLMozdziakPJesetaMMachatkovaMKrancWKempistyBOvarian follicular cells - Living in the shadow of stemness cellular competence201971344010.2478/acb-2019-0018Open DOISearch in Google Scholar
Zeng H, Qin L, Zhao D, Tan X, Manseau EJ, Mien VH, Senger DR, Brown LF, Nagy JA, Dvorak HF. Orphan nuclear receptor TR3/Nur77 regulates VEGF-A-induced angiogenesis through its transcriptional activity. J Exp Med. 2006;203:719–29; DOI:10.1084/jem.20051523.ZengHQinLZhaoDTanXManseauEJMienVHSengerDRBrownLFNagyJADvorakHFOrphan nuclear receptor TR3/Nur77 regulates VEGF-A-induced angiogenesis through its transcriptional activity20062037192910.1084/jem.20051523211824516520388Open DOISearch in Google Scholar
Gao X, Zhang J, Pan Z, Li Q, Liu H. The distribution and expression of vascular endothelial growth factor A (VEGFA) during follicular development and atresia in the pig. Reprod Fertil Dev. 2020;32:259; DOI:10.1071/RD18508.GaoXZhangJPanZLiQLiuHThe distribution and expression of vascular endothelial growth factor A (VEGFA) during follicular development and atresia in the pig20203225910.1071/RD1850831545934Open DOISearch in Google Scholar
Farioli-Vecchioli S, Micheli L, Ceccarelli M, Leonardi L, Tirone F. Genetic control of adult neurogenesis: Interplay of differentiation, proliferation and survival modulates new neurons function and memory circuits. Front Cell Neurosci. 2013; DOI:10.3389/fncel.2013.00059.Farioli-VecchioliSMicheliLCeccarelliMLeonardiLTironeFGenetic control of adult neurogenesis: Interplay of differentiation, proliferation and survival modulates new neurons function and memory circuits201310.3389/fncel.2013.00059365309823734097Open DOISearch in Google Scholar
Li F, Liu J, Park ES, Jo M, Curry TE. The B cell translocation gene (BTG) family in the rat ovary: Hormonal induction, regulation, and impact on cell cycle kinetics. Endocrinology. 2009;150:3894–902; DOI:10.1210/en.2008-1650.LiFLiuJParkESJoMCurryTEThe B cell translocation gene (BTG) family in the rat ovary: Hormonal induction, regulation, and impact on cell cycle kinetics2009150389490210.1210/en.2008-1650271785719359386Open DOISearch in Google Scholar
Martina JA, Lelouvier B, Puertollano R. The Calcium Channel Mucolipin-3 is a Novel Regulator of Trafficking Along the Endosomal Pathway. Traffic. 2009;10:1143–56; DOI:10.1111/j.1600-0854.2009.00935.x.MartinaJALelouvierBPuertollanoRThe Calcium Channel Mucolipin-3 is a Novel Regulator of Trafficking Along the Endosomal Pathway20091011435610.1111/j.1600-0854.2009.00935.x295585919497048Open DOISearch in Google Scholar
Martina JA, Lelouvier B, Puertollano R. The calcium channel mucolipin-3 is a novel regulator of trafficking along the endosomal pathway. Traffic. 2009;10:1143–56; DOI:10.1111/j.1600-0854.2009.00935.x.MartinaJALelouvierBPuertollanoRThe calcium channel mucolipin-3 is a novel regulator of trafficking along the endosomal pathway20091011435610.1111/j.1600-0854.2009.00935.xOpen DOISearch in Google Scholar
Kulus M, Sujka-kordowska P, Konwerska A, Celichowski P, Kranc W, Kulus J, Piotrowska-kempisty H, Antosik P. New Molecular Markers Involved in Regulation of Ovarian Granulosa Cell Morphogenesis , Development and Di ff erentiation during Short-Term Primary In vitro Culture — Transcriptomic and Histochemical Study Based on Ovaries and Individual Separated Follicle. Int J Mol Sci. 2019;20:3966; DOI:doi:10.3390/ijms20163966.KulusMSujka-kordowskaPKonwerskaACelichowskiPKrancWKulusJPiotrowska-kempistyHAntosikP New Molecular Markers Involved in Regulation of Ovarian Granulosa Cell Morphogenesis , Development and Di ff erentiation during Short-Term Primary In vitro Culture — Transcriptomic and Histochemical Study Based on Ovaries and Individual Separated Follicle2019203966 DOI:doi10.3390/ijms20163966672100131443152Open DOISearch in Google Scholar
LeBlanc SE, Srinivasan R, Ferri C, Mager GM, Gillian-Daniel AL, Wrabetz L, Svaren J. Regulation of cholesterol/lipid biosynthetic genes by Egr2/Krox20 during peripheral nerve myelination. J Neurochem. 2005;93:737–48; DOI:10.1111/j.1471-4159.2005.03056.x.LeBlancSESrinivasanRFerriCMagerGMGillian-DanielALWrabetzLSvarenJRegulation of cholesterol/lipid biosynthetic genes by Egr2/Krox20 during peripheral nerve myelination2005937374810.1111/j.1471-4159.2005.03056.x15836632Open DOISearch in Google Scholar
Jang S-W, LeBlanc SE, Roopra A, Wrabetz L, Svaren J. In vitro detection of Egr2 binding to target genes during peripheral nerve myelination. J Neurochem. 2006;98:1678–87; DOI:10.1111/j.1471-4159.2006.04069.x.JangS-WLeBlancSERoopraAWrabetzLSvarenJIn vitro detection of Egr2 binding to target genes during peripheral nerve myelination20069816788710.1111/j.1471-4159.2006.04069.x16923174Open DOISearch in Google Scholar
Topilko P, Schneider-Maunoury S, Levi G, Baron-Van Evercooren A, Chennoufi ABY, Seitanidou T, Babinet C, Charnay P. Krox-20 controls myelination in the peripheral nervous system. Nature. 1994;371:796–9; DOI:10.1038/371796a0.TopilkoPSchneider-MaunourySLeviGBaron-Van EvercoorenAChennoufiABYSeitanidouTBabinetCCharnayPKrox-20 controls myelination in the peripheral nervous system1994371796910.1038/371796a0Open DOISearch in Google Scholar
Jin H, Won M, Shin E, Kim HM, Lee K, Bae J. EGR2 is a gonadotropin-in-duced survival factor that controls the expression of IER3 in ovarian granulosa cells. Biochem Biophys Res Commun. 2017;482:877–82; DOI:10.1016/j.bbrc.2016.11.127.JinHWonMShinEKimHMLeeKBaeJEGR2 is a gonadotropin-in-duced survival factor that controls the expression of IER3 in ovarian granulosa cells20174828778210.1016/j.bbrc.2016.11.127Open DOISearch in Google Scholar
Brązert M, Kranc W, Nawrocki MJ, Sujka–Kordowska P, Konwerska A, Jankowski M, Kocherova I, Celichowski P, Jeseta M, Ożegowska K, Antosik P, Bukowska D, Skowroński MT, Bruska M, Pawelczyk L, Zabel M, Piotrowska–Kempisty H, Nowicki M, Kempisty B. New markers for regulation of transcription and macromolecule metabolic process in porcine oocytes during in vitro maturation. Mol Med Rep. 2020;21:1537–51; DOI:10.3892/mmr.2020.10963.BrązertMKrancWNawrockiMJSujka–KordowskaPKonwerskaAJankowskiMKocherovaICelichowskiPJesetaMOżegowskaKAntosikPBukowskaDSkowrońskiMTBruskaMPawelczykLZabelMPiotrowska–KempistyHNowickiMKempistyBNew markers for regulation of transcription and macromolecule metabolic process in porcine oocytes during in vitro maturation20202115375110.3892/mmr.2020.10963Open DOISearch in Google Scholar
Stenvers KL, Tursky ML, Harder KW, Kountouri N, Amatayakul-Chantler S, Grail D, Small C, Weinberg RA, Sizeland AM, Zhu H-J. Heart and Liver Defects and Reduced Transforming Growth Factor 2 Sensitivity in Transforming Growth Factor Type III Receptor-Deficient Embryos. Mol Cell Biol. 2003;23:4371–85; DOI:10.1128/mcb.23.12.4371-4385.2003.StenversKLTurskyMLHarderKWKountouriNAmatayakul-ChantlerSGrailDSmallCWeinbergRASizelandAMZhuH-J.Heart and Liver Defects and Reduced Transforming Growth Factor 2 Sensitivity in Transforming Growth Factor Type III Receptor-Deficient Embryos20032343718510.1128/mcb.23.12.4371-4385.2003Open DOISearch in Google Scholar
Kranc W, Budna J, Chachuła A, Borys S, Bryja A, Rybska M, Ciesiółka S, Sumelka E, Jeseta M, Brüssow KP, Bukowska D, Antosik P, Bruska M, Nowicki M, Zabel M, Kempisty B. Cell Migration Is the Ontology Group Differentially Expressed in Porcine Oocytes before and after in vitro Maturation: A Microarray Approach. DNA Cell Biol. 2017;36:273–82; DOI:10.1089/dna.2016.3425.KrancWBudnaJChachułaABorysSBryjaARybskaMCiesiółkaSSumelkaEJesetaMBrüssowKPBukowskaDAntosikPBruskaMNowickiMZabelMKempistyBCell Migration Is the Ontology Group Differentially Expressed in Porcine Oocytes before and after in vitro Maturation: A Microarray Approach2017362738210.1089/dna.2016.3425Open DOISearch in Google Scholar
Fu Y, Zhang S-S, Xiao S, Basheer WA, Baum R, Epifantseva I, Hong T, Shaw RM. Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport. Front Physiol. 2017;8:905; DOI:10.3389/fphys.2017.00905.FuYZhangS-SXiaoSBasheerWABaumREpifantsevaIHongTShawRMCx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport2017890510.3389/fphys.2017.00905Open DOISearch in Google Scholar
Santiago MF, Alcami P, Striedinger KM, Spray DC, Scemes E. The carboxyl-terminal domain of Connexin43 is a negative modulator of neuronal differentiation. J Biol Chem. 2010;285:11836–45; DOI:10.1074/jbc. M109.058750.SantiagoMFAlcamiPStriedingerKMSprayDCScemesEThe carboxyl-terminal domain of Connexin43 is a negative modulator of neuronal differentiation2010285118364510.1074/jbc.M109.058750Open DOISearch in Google Scholar
Involvement of GJA1 and Gap Junctional Intercellular Communication between Cumulus Cells and Oocytes from Women with PCOS n.d.https://www.hindawi.com/journals/bmri/2020/5403904/ (accessed March 10, 2020).n.dhttps://www.hindawi.com/journals/bmri/2020/5403904/accessed March 10202010.1155/2020/5403904Search in Google Scholar
Ying SY, Becker A, Swanson G, Tan P, Ling N, Esch F, Ueno N, Shimasaki S, Guillemin R. Follistatin specifically inhibits pituitary follicle stimulating hormone release invitro. Biochem Biophys Res Commun. 1987;149:133–9; DOI:10.1016/0006-291X(87)91614-7.YingSYBeckerASwansonGTanPLingNEschFUenoNShimasakiSGuilleminRFollistatin specifically inhibits pituitary follicle stimulating hormone release invitro1987149133910.1016/0006-291X(87)91614-7Open DOISearch in Google Scholar
Nakamura T, Hasegawa Y, Sugino K, Kogawa K, Titani K, Sugino H. Follistatin inhibits activin-induced differentiation of rat follicular granulosa cells in vitro. BBA - Mol Cell Res. 1992;1135:103–9; DOI:10.1016/0167-4889(92)90173-9.NakamuraTHasegawaYSuginoKKogawaKTitaniKSuginoHFollistatin inhibits activin-induced differentiation of rat follicular granulosa cells in vitro19921135103910.1016/0167-4889(92)90173-9Open DOISearch in Google Scholar
Dragovic RA, Ritter LJ, Schulz SJ, Amato F, Thompson JG, Armstrong DT, Gilchrist RB. Oocyte-Secreted Factor Activation of SMAD 2/3 Signaling Enables Initiation of Mouse Cumulus Cell Expansion1. Biol Reprod. 2007;76:848–57; DOI:10.1095/biolreprod.106.057471.DragovicRARitterLJSchulzSJAmatoFThompsonJGArmstrongDTGilchristRBOocyte-Secreted Factor Activation of SMAD 2/3 Signaling Enables Initiation of Mouse Cumulus Cell Expansion12007768485710.1095/biolreprod.106.05747117192514Open DOISearch in Google Scholar
Ashry M, Lee K, Mondal M, Datta TK, Folger JK, Rajput SK, Zhang K, Hemeida NA, Smith GW. Expression of TGFβ superfamily components and other markers of oocyte quality in oocytes selected by brilliant cresyl blue staining: Relevance to early embryonic development. Mol Reprod Dev. 2015;82:251–64; DOI:10.1002/mrd.22468.AshryMLeeKMondalMDattaTKFolgerJKRajputSKZhangKHemeidaNASmithGWExpression of TGFβ superfamily components and other markers of oocyte quality in oocytes selected by brilliant cresyl blue staining: Relevance to early embryonic development2015822516410.1002/mrd.22468440781225704641Open DOISearch in Google Scholar
Guo Z, Islam MS, Liu D, Liu G, Lv L, Yang Y, Fu B, Wang L, Liu Z, He H, Wu H. Differential effects of follistatin on porcine oocyte competence and cumulus cell gene expression in vitro. Reprod Domest Anim. 2018;53:3–10; DOI:10.1111/rda.13035.GuoZIslamMSLiuDLiuGLvLYangYFuBWangLLiuZHeHWuHDifferential effects of follistatin on porcine oocyte competence and cumulus cell gene expression in vitro20185331010.1111/rda.1303529134682Open DOISearch in Google Scholar
Terracciano A, Esko T, Sutin AR, De Moor MHM, Meirelles O, Zhu G, Tanaka T, Giegling I, Nutile T, Realo A, Allik J, Hansell NK, Wright MJ, Montgomery GW, Willemsen G, Hottenga JJ, Friedl M, Ruggiero D, Sorice R, Sanna S, Cannas A, Räikkönen K, Widen E, Palotie A, Eriksson JG, Cucca F, Krueger RF, Lahti J, Luciano M, Smoller JW, Van Duijn CM, Abecasis GR, Boomsma DI, Ciullo M, Costa PT, Ferrucci L, Martin NG, Metspalu A, Rujescu D, Schlessinger D, Uda M. Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Transl Psychiatry. 2011;1:e49–e49; DOI:10.1038/tp.2011.42.TerraccianoAEskoTSutinARDe MoorMHMMeirellesOZhuGTanakaTGieglingINutileTRealoAAllikJHansellNKWrightMJMontgomeryGWWillemsenGHottengaJJFriedlMRuggieroDSoriceRSannaSCannasARäikkönenKWidenEPalotieAErikssonJGCuccaFKruegerRFLahtiJLucianoMSmollerJWVan DuijnCMAbecasisGRBoomsmaDICiulloMCostaPTFerrucciLMartinNGMetspaluARujescuDSchlessingerDUdaMMeta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking20111e49e4910.1038/tp.2011.42330949322833195Open DOISearch in Google Scholar
Schaffer AE, Breuss MW, Caglayan AO, Al-Sanaa N, Al-Abdulwahed HY, Kaymakçalan H, Yılmaz C, Zaki MS, Rosti RO, Copeland B, Baek ST, Musaev D, Scott EC, Ben-Omran T, Kariminejad A, Kayserili H, Mojahedi F, Kara M, Cai N, Silhavy JL, Elsharif S, Fenercioglu E, Barshop BA, Kara B, Wang R, Stanley V, James KN, Nachnani R, Kalur A, Megahed H, Incecik F, Danda S, Alanay Y, Faqeih E, Melikishvili G, Mansour L, Miller I, Sukhudyan B, Chelly J, Dobyns WB, Bilguvar K, Jamra RA, Gunel M, Gleeson JG. Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration. Nat Genet. 2018;50:1093–101; DOI:10.1038/s41588-018-0166-0.SchafferAEBreussMWCaglayanAOAl-SanaaNAl-AbdulwahedHYKaymakçalanHYılmazCZakiMSRostiROCopelandBBaekSTMusaevDScottECBen-OmranTKariminejadAKayseriliHMojahediFKaraMCaiNSilhavyJLElsharifSFenerciogluEBarshopBAKaraBWangRStanleyVJamesKNNachnaniRKalurAMegahedHIncecikFDandaSAlanayYFaqeihEMelikishviliGMansourLMillerISukhudyanBChellyJDobynsWBBilguvarKJamraRAGunelMGleesonJGBiallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration201850109310110.1038/s41588-018-0166-0607255530013181Open DOISearch in Google Scholar
Budna J, Celichowski P, Bryja A, Dyszkiewicz-Konwińska M, Jeseta M, Bukowska D, Antosik P, Brüssow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. Significant down-regulation of “biological adhesion” genes in porcine oocytes after IVM. Int J Mol Sci. 2017;18:2685; DOI:10.3390/ijms18122685.BudnaJCelichowskiPBryjaADyszkiewicz-KonwińskaMJesetaMBukowskaDAntosikPBrüssowKPBruskaMNowickiMZabelMKempistyBSignificant down-regulation of “biological adhesion” genes in porcine oocytes after IVM201718268510.3390/ijms18122685575128729232894Open DOISearch in Google Scholar
Chi C, Liu N, Yue L, Qi W-W, Xu L-L, Qiu W-S. RTN4/Nogo is an independent prognostic marker for gastric cancer: preliminary results. Eur Rev Med Pharmacol Sci. 2015;19:241–6.ChiCLiuNYueLQiW-WXuL-LQiuW-SRTN4/Nogo is an independent prognostic marker for gastric cancer: preliminary results2015192416Search in Google Scholar
Teng FYH, Tang BL. Nogo/RTN4 isoforms and RTN3 expression protect SH-SY5Y cells against multiple death insults. Mol Cell Biochem. 2013;384:7–19; DOI:10.1007/s11010-013-1776-6.TengFYHTangBLNogo/RTN4 isoforms and RTN3 expression protect SH-SY5Y cells against multiple death insults201338471910.1007/s11010-013-1776-623955438Open DOISearch in Google Scholar
Kranc W, Budna J, Chachuła A, Borys S, Bryja A, Rybska M, Ciesiółka S, Sumelka E, Jeseta M, Brüssow KP, Bukowska D, Antosik P, Bruska M, Nowicki M, Zabel M, Kempisty B. “Cell Migration” Is the Ontology Group Differentially Expressed in Porcine Oocytes Before and After In vitro Maturation: A Microarray Approach. DNA Cell Biol. 2017;36:273–82; DOI:10.1089/dna.2016.3425.KrancWBudnaJChachułaABorysSBryjaARybskaMCiesiółkaSSumelkaEJesetaMBrüssowKPBukowskaDAntosikPBruskaMNowickiMZabelMKempistyB.“Cell Migration” Is the Ontology Group Differentially Expressed in Porcine Oocytes Before and After In vitro Maturation: A Microarray Approach2017362738210.1089/dna.2016.342528384068Open DOISearch in Google Scholar
Takeuchi A, O’Leary DDM. Radial migration of superficial layer cortical neurons controlled by novel Ig cell adhesion molecule MDGA1. J Neurosci. 2006;26:4460–4; DOI:10.1523/JNEUROSCI.4935-05.2006.TakeuchiAO’LearyDDMRadial migration of superficial layer cortical neurons controlled by novel Ig cell adhesion molecule MDGA12006264460410.1523/JNEUROSCI.4935-05.2006667406516641224Open DOISearch in Google Scholar
Kähler AK, Djurovic S, Kulle B, Jönsson EG, Agartz I, Hall H, Opjordsmoen S, Jakobsen KD, Hansen T, Melle I, Werge T, Steen VM, Andreassen OA. Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene. Am J Med Genet Part B Neuropsychiatr Genet. 2008;147:1089–100; DOI:10.1002/ajmg.b.30726.KählerAKDjurovicSKulleBJönssonEGAgartzIHallHOpjordsmoenSJakobsenKDHansenTMelleIWergeTSteenVMAndreassenOAAssociation analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene2008147108910010.1002/ajmg.b.3072618384059Open DOISearch in Google Scholar
Driancourt MA, Reynaud K, Cortvrindt R, Smitz J. Roles of KIT and KIT LIGAND in ovarian function. Rev Reprod. 2000;5:143–52; DOI:10.1530/ror.0.0050143.DriancourtMAReynaudKCortvrindtRSmitzJRoles of KIT and KIT LIGAND in ovarian function200051435210.1530/ror.0.005014311006164Open DOISearch in Google Scholar
Conde P, Morado S, Alvarez G, Smitz J, Gentile T, Cetica P. Effect of the hematopoietic growth factors erythropoietin and kit ligand on bovine oocyte in vitro maturation and developmental competence. Theriogenology. 2019;123:37–44; DOI:10.1016/j.theriogenology.2018.09.014.CondePMoradoSAlvarezGSmitzJGentileTCeticaPEffect of the hematopoietic growth factors erythropoietin and kit ligand on bovine oocyte in vitro maturation and developmental competence2019123374410.1016/j.theriogenology.2018.09.01430273739Open DOISearch in Google Scholar
Xu B, Zhang YW, Tong XH, Liu YS. Characterization of microRNA profile in human cumulus granulosa cells: Identification of microRNAs that regulate Notch signaling and are associated with PCOS. Mol Cell Endocrinol. 2015;404:26–36; DOI:10.1016/j.mce.2015.01.030.XuBZhangYWTongXHLiuYSCharacterization of microRNA profile in human cumulus granulosa cells: Identification of microRNAs that regulate Notch signaling and are associated with PCOS2015404263610.1016/j.mce.2015.01.03025622783Open DOISearch in Google Scholar
Sun T, Diaz FJ. Ovulatory signals alter granulosa cell behavior through YAP1 signaling. Reprod Biol Endocrinol. 2019;17:1–14; DOI:10.1186/s12958-019-0552-1.SunTDiazFJOvulatory signals alter granulosa cell behavior through YAP1 signaling20191711410.1186/s12958-019-0552-1693517731883523Open DOISearch in Google Scholar
Chang WH, Choi SH, Moon BS, Cai M, Lyu J, Bai J, Gao F, Hajjali I, Zhao Z, Campbell DB, Weiner LP, Lu W. Smek1/2 is a nuclear chaperone and cofactor for cleaved Wnt receptor Ryk, regulating cortical neurogenesis. Proc Natl Acad Sci U S A. 2017;114:E10717–25; DOI:10.1073/pnas.1715772114.ChangWHChoiSHMoonBSCaiMLyuJBaiJGaoFHajjaliIZhaoZCampbellDBWeinerLPLuWSmek1/2 is a nuclear chaperone and cofactor for cleaved Wnt receptor Ryk, regulating cortical neurogenesis2017114E107172510.1073/pnas.1715772114574065129180410Open DOISearch in Google Scholar
Budna J, Bryja A, Celichowski P, Kahan R, Kranc W, Ciesiółka S, Rybska M, Borys S, Jeseta M, Bukowska D, Antosik P, Brüssow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. Genes of cellular components of morphogenesis in porcine oocytes before and after IVM. Reproduction. 2017;154:535–45; DOI:10.1530/REP-17-0367.BudnaJBryjaACelichowskiPKahanRKrancWCiesiółkaSRybskaMBorysSJesetaMBukowskaDAntosikPBrüssowKPBruskaMNowickiMZabelMKempistyBGenes of cellular components of morphogenesis in porcine oocytes before and after IVM20171545354510.1530/REP-17-036728733345Open DOISearch in Google Scholar
Kranc W, Celichowski P, Budna J, Khozmi R, Bryja A, Ciesiółka S, Rybska M, Borys S, Jeseta M, Bukowska D, Antosik P, Brüssow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. Positive regulation of macromolecule metabolic process belongs to the main mechanisms crucial for porcine oocytes maturation. Adv Cell Biol. 2017;5:15–31; DOI:10.1515/acb-2017-0002.KrancWCelichowskiPBudnaJKhozmiRBryjaACiesiółkaSRybskaMBorysSJesetaMBukowskaDAntosikPBrüssowKPBruskaMNowickiMZabelMKempistyBPositive regulation of macromolecule metabolic process belongs to the main mechanisms crucial for porcine oocytes maturation20175153110.1515/acb-2017-0002Open DOISearch in Google Scholar
Kawaguchi-Niida M, Shibata N, Furuta Y. Smad4 is essential for directional progression from committed neural progenitor cells through neuronal differentiation in the postnatal mouse brain. Mol Cell Neurosci. 2017;83:55–64; DOI:10.1016/j.mcn.2017.06.008.Kawaguchi-NiidaMShibataNFurutaYSmad4 is essential for directional progression from committed neural progenitor cells through neuronal differentiation in the postnatal mouse brain201783556410.1016/j.mcn.2017.06.00828669622Open DOISearch in Google Scholar
Xing N, Liang Y, Gao Z, He J, He X, Li H, Dong C. Expression and localization of Smad2 and Smad4 proteins in the porcine ovary. Acta Histochem. 2014;116:1301–6; DOI:10.1016/j.acthis.2014.07.014.XingNLiangYGaoZHeJHeXLiHDongCExpression and localization of Smad2 and Smad4 proteins in the porcine ovary20141161301610.1016/j.acthis.2014.07.01425190106Open DOISearch in Google Scholar
Goldberg JL, Vargas ME, Wang JT, Mandemakers W, Oster SF, Sretavan DW, Barres BA. An oligodendrocyte lineage-specific semaphorin, sema5A, inhibits axon growth by retinal ganglion cells. J Neurosci. 2004;24:4989–99; DOI:10.1523/JNEUROSCI.4390-03.2004.GoldbergJLVargasMEWangJTMandemakersWOsterSFSretavanDWBarresBAAn oligodendrocyte lineage-specific semaphorin, sema5A, inhibits axon growth by retinal ganglion cells20042449899910.1523/JNEUROSCI.4390-03.2004672938015163691Open DOISearch in Google Scholar
Nawrocki M, Celichowski P, Budna J, Bryja A, Kranc W, Ciesiółka S, Borys S, Knap S, Jeseta M, Khozmii R, Bukowska D, Antosik P, Brussow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. The blood vessels development, morphogenesis and blood circulation are three ontologic groups highly up-regulated in porcine oocytes before in vitro. Med J Cell Biol. 2017;5:135–142; DOI:10.1515/acb-2017-0012.NawrockiMCelichowskiPBudnaJBryjaAKrancWCiesiółkaSBorysSKnapSJesetaMKhozmiiRBukowskaDAntosikPBrussowKPBruskaMNowickiMZabelMKempistyBThe blood vessels development, morphogenesis and blood circulation are three ontologic groups highly up-regulated in porcine oocytes before in vitro2017513514210.1515/acb-2017-0012Open DOISearch in Google Scholar
Goodwin LR, Picketts DJ. The role of ISWI chromatin remodeling complexes in brain development and neurodevelopmental disorders. Mol Cell Neurosci. 2018;87:55–64; DOI:10.1016/j.mcn.2017.10.008.GoodwinLRPickettsDJThe role of ISWI chromatin remodeling complexes in brain development and neurodevelopmental disorders201887556410.1016/j.mcn.2017.10.00829249292Open DOISearch in Google Scholar
Bergström P, Agholme L, Nazir FH, Satir TM, Toombs J, Wellington H, Strandberg J, Bontell TO, Kvartsberg H, Holmström M, Boreström C, Simonsson S, Kunath T, Lindahl A, Blennow K, Hanse E, Portelius E, Wray S, Zetterberg H. Amyloid precursor protein expression and processing are differentially regulated during cortical neuron differentiation. Sci Rep. 2016;6:1–14; DOI:10.1038/srep29200.BergströmPAgholmeLNazirFHSatirTMToombsJWellingtonHStrandbergJBontellTOKvartsbergHHolmströmMBoreströmCSimonssonSKunathTLindahlABlennowKHanseEPorteliusEWraySZetterbergHAmyloid precursor protein expression and processing are differentially regulated during cortical neuron differentiation2016611410.1038/srep29200493587727383650Open DOISearch in Google Scholar