Genome-wide association study for single nucleotide polymorphism associated with mural and cumulus granulosa cells of PCOS (polycystic ovary syndrome) and non-PCOS patients

Qazvini NT, Zinatloo S (2011) Synthesis and characterization of gelatin nanoparticles using CDI/NHS as a non-toxic cross-linking system. J Mater Sci: Mater Med 22(1):63–69. https://doi.org/10.1007/s10856-010-4178-2

Article  CAS  PubMed  Google Scholar 

Zinatloo-Ajabshir S, Qazvinia NT (2014) Inverse miniemulsion method for synthesis of gelatin nanoparticles in presence of CDI/NHS as a non-toxic cross-linking system. J Nanostruct 4:267–275. https://doi.org/10.7508/jns.2014.03.003

Article  Google Scholar 

Zinatloo-Ajabshir S, Taheri Qazvini N (2015) Effect of some synthetic parameters on size and polydispersity index of gelatin nanoparticles cross-linked by CDI/NHS system. J Nanostruct 5(2):137–144. https://doi.org/10.7508/jns.2015.02.008

Article  Google Scholar 

Zinatloo-Ajabshir Z, Zinatloo-Ajabshir S (2019) Preparation and characterization of curcumin niosomal nanoparticles via a simple and eco-friendly route. J Nanostruct 9(4):784–790. https://doi.org/10.22052/JNS.2019.04.020

Article  CAS  Google Scholar 

Zinatloo-Ajabshir S, Heidari-Asil SA, Salavati-Niasari M (2022) Rapid and green combustion synthesis of nanocomposites based on Zn–Co–O nanostructures as photocatalysts for enhanced degradation of acid brown 14 contaminant under sunlight. Sep Purif Technol 280:119841. https://doi.org/10.1016/j.seppur.2021.119841

Article  CAS  Google Scholar 

Mahdavi K, Zinatloo-Ajabshir S, Yousif QA, Salavati-Niasari M (2022) Enhanced photocatalytic degradation of toxic contaminants using Dy2O3-SiO2 ceramic nanostructured materials fabricated by a new, simple and rapid sonochemical approach. Ultrason Sonochem 82:105892. https://doi.org/10.1016/j.ultsonch.2021.105892

Article  CAS  PubMed  Google Scholar 

Hosseinzadeh G, Ghasemian N, Zinatloo-Ajabshir S (2022) TiO2/graphene nanocomposite supported on clinoptilolite nanoplate and its enhanced visible light photocatalytic activity. Inorg Chem Commun 136:109144. https://doi.org/10.1016/j.inoche.2021.109144

Article  CAS  Google Scholar 

Tabatabaeinejada SM, Zinatloo-Ajabshir S, Amiric O, Salavati-Niasari M (2021) Magnetic Lu2Cu2O5-based ceramic nanostructured materials fabricated by a simple and green approach for an effective photocatalytic degradation of organic contamination. RSC Adv 11:40100–40111. https://doi.org/10.1039/d1ra06101a

Article  CAS  Google Scholar 

Zinatloo-Ajabshir S, Heidari-Asil SA, Salavati-Niasari M (2021) Simple and eco-friendly synthesis of recoverable zinc cobalt oxide-based ceramic nanostructure as high-performance photocatalyst for enhanced photocatalytic removal of organic contamination under solar light. Sep Purif Technol 267:118667. https://doi.org/10.1016/j.seppur.2021.118667

Article  CAS  Google Scholar 

Salehi Z, Zinatloo-Ajabshir S, Salavati-Niasari M (2016) Novel synthesis of Dy2Ce2O7 nanostructures via a facile combustion route. RSC Adv 6:26895–26901. https://doi.org/10.1039/C5RA27919D

Article  CAS  Google Scholar 

Chang M, He L, Cai L (2018) An Overview of Genome-Wide Association Studies. Methods Mol Biol 1754:97–108. https://doi.org/10.1007/978-1-4939-7717-8_6

Article  CAS  PubMed  Google Scholar 

Wellcome Trust Case Control Consortium (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447(7145):661–678. https://doi.org/10.1038/nature05911

Article  CAS  Google Scholar 

Khatri B, Tessneer KL, Rasmussen A, Aghakhanian F, Reksten TR, Adler A, Alevizos I, Anaya JM, Aqrawi LA, Baecklund E, Brun JG, Bucher SM, Eloranta ML, Engelke F, Forsblad-d’Elia H, Glenn SB, Hammenfors D, Imgenberg-Kreuz J, Jensen JL, Johnsen SJA, Lessard CJ (2022) Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells. Nat Commun 13(1):4287. https://doi.org/10.1038/s41467-022-30773-y

Article  CAS  PubMed  PubMed Central  Google Scholar 

Vijayan SM, Kalaivani H, Mitra S, John J, Anila A, Damini Boban L, Chowdhury P, Gayen S (2022) Barriers to treatment regimen adherence in Indian women with polycystic ovarian syndrome. J Fam Med Prim Care 11:3687–3692. https://doi.org/10.4103/jfmpc.jfmpc_2360_21

Article  Google Scholar 

Zhu YN, Zhang YT, Liu Q, Shen SM, Zou X, Cao YX (2020) Association analysis between the tag single nucleotide polymorphisms of DENND1A and the risk of polycystic ovary syndrome in Chinese Han women. BMC Med Genet 21(1):14. https://doi.org/10.1186/s12881-019-0945-1

Article  CAS  PubMed  PubMed Central  Google Scholar 

Shukla P, Mukherjee S, Patil A, Joshi B (2022) Molecular characterization of variants in mitochondrial DNA encoded genes using next generation sequencing analysis and mitochondrial dysfunction in women with PCOS. Gene 855:147126. https://doi.org/10.1016/j.gene.2022.147126

Article  CAS  PubMed  Google Scholar 

Karen Nenonene E, Trottier-Lavoie M, Marchais M, Bastien A, Gilbert I, Macaulay AD, Khandjian EW, Maria Luciano A, Lodde V, Viger RS, Robert C (2023) Roles of the cumulus-oocyte transzonal network and the Fragile X protein family in oocyte competence. Reproduction (Cambridge, England) 165(2):209–219. https://doi.org/10.1530/REP-22-0165

Article  PubMed  Google Scholar 

Chen L, Hu M, Wang F, Yang Y, Huang Y, Zhou W, Sun X (2017) Genome-wide association study for SNPs associated with PCOS in human patients. Exp Ther Med 14(5):4896–4900. https://doi.org/10.3892/etm.2017.5113

Article  CAS  PubMed  PubMed Central  Google Scholar 

Dai W, Zou X, Jia H, Peng Y, La B, Yan Z, Gao L, Qin L, Diao F, Ma X, Meng Y, Cui Y, Liu J (2022) Peroxiredoxin 4 secreted by cumulus cells ameliorates the maturation of oocytes in vitro. Biochem Biophys Res Commun 636(Pt 1):155–161. https://doi.org/10.1016/j.bbrc.2022.10.073

Article  CAS  PubMed  Google Scholar 

Nagy RA, van Montfoort A, Tietge U, Terpstra M, Kok K, van den Berg A, Hoek A, Kluiver J, Donker R (2019) Differential miRNA expression profiles in cumulus and mural granulosa cells from human pre-ovulatory follicles. Microrna 8(1):61–67. https://doi.org/10.2174/2211536607666180912152618

Article  CAS  PubMed  PubMed Central  Google Scholar 

Karakaya C, Guzeloglu-Kayisli O, Hobbs RJ, Gerasimova T, Uyar A, Erdem M, Oktem M, Erdem A, Gumuslu S, Ercan D, Sakkas D, Comizzoli P, Seli E, Lalioti MD (2014) Follicle-stimulating hormone receptor (FSHR) alternative skipping of exon 2 or 3 affects ovarian response to FSH. Mol Hum Reprod 20(7):630–643. https://doi.org/10.1093/molehr/gau024

Article  CAS  PubMed  PubMed Central  Google Scholar 

Han Y, Gao G, Li S, Xiao N, Zhang Y, Luo H (2021) Development of an optimal protocol for isolation and purification of human granulosa cells in patients with different ovarian reserves. Exp Ther Med 22(3):938. https://doi.org/10.3892/etm.2021.10370

Article  CAS  PubMed  PubMed Central  Google Scholar 

Diefenbach RJ, Lee JH, Kefford RF, Rizos H (2018) Evaluation of commercial kits for purification of circulating free DNA. Cancer Genet 228–229:21–27. https://doi.org/10.1016/j.cancergen.2018.08.005

Article  CAS  PubMed  Google Scholar 

Andrei D, Nagy RA, van Montfoort A, Tietge U, Terpstra M, Kok K, van den Berg A, Hoek A, Kluiver J, Donker R (2018) An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region. PeerJ 6:e4816. https://doi.org/10.7717/peerj.4816

Article  CAS  Google Scholar 

Santos K, Preussner M, Heroven AC, Weber G (2015) Crystallization and biochemical characterization of the human spliceosomal Aar2–Prp8RNaseH complex. Acta Crystallogr F Struct Biol Commun 71(Pt 11):1421–1428. https://doi.org/10.1107/S2053230X15019202

Article  CAS  PubMed  PubMed Central  Google Scholar 

Peralta S, González-Quintana A, Ybarra M, Delmiro A, Pérez-Pérez R, Docampo J, Arenas J, Blázquez A, Ugalde C, Martín MA (2019) Novel ATAD3A recessive mutation associated to fatal cerebellar hypoplasia with multiorgan involvement and mitochondrial structural abnormalities. Mol Genet Metab 128(4):452–462. https://doi.org/10.1016/j.ymgme.2019.10.012

Article  CAS  PubMed  Google Scholar 

Nomoto H, Oohashi T, Hirakawa S, Ueki Y, Ohtsuki H, Ninomiya Y (2002) Human BRAL1 and BCAN genes that belong to the link-module superfamily are tandemly arranged on chromosome 1q21-23. Acta Med Okayama 56(1):25–29. https://doi.org/10.18926/AMO/31728

Article  CAS  PubMed  Google Scholar 

Hiatt SM, Thompson ML, Prokop JW, Lawlor JMJ, Gray DE, Bebin EM, Rinne T, Kempers M, Pfundt R, van Bon BW, Mignot C, Nava C, Depienne C, Kalsner L, Rauch A, Joset P, Bachmann-Gagescu R, Wentzensen IM, McWalter K, Cooper GM (2019) Deleterious variation in BRSK2 associates with a neurodevelopmental disorder. Am J Hum Genet 104(4):701–708. https://doi.org/10.18926/AMO/31728

Article  CAS  PubMed  PubMed Central  Google Scholar 

Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics; Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study; Hedrich UBS, Scheffer IE, Helbig I, Zamponi GW, Lerche H, Mefford HC (2018) De novo pathogenic variants in CACNA1E cause developmental and epileptic encephalopathy with contractures, macrocephaly, and dyskinesias. Am J Hum Genet 103(5):666–678. https://doi.org/10.1016/j.ajhg.2018.09.006

Don AS, Rosen H (2009) A lipid binding domain in sphingosine kinase 2. Biochem Biophys Res Commun 380(1):87–92. https://doi.org/10.1016/j.bbrc.2009.01.075

Article  CAS  PubMed  PubMed Central  Google Scholar 

Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, Szpyt J, Gassaway BM, Panov A, Parzen H, Fu S, Golbazi A, Maenpaa E, Stricker K, Guha Thakurta S, Zhang T, Rad R, Pan J, Nusinow DP, Paulo JA, Schweppe DK, Vaites LP, Harper JW, Gygi SP (2021) Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. Cell 184(11):3022-3040.e28. https://doi.org/10.1016/j.cell.2021.04.011

Article  CAS  PubMed  PubMed Central  Google Scholar 

Parenti I, Lehalle D, Nava C, Torti E, Leitão E, Person R, Mizuguchi T, Matsumoto N, Kato M, Nakamura K, de Man SA, Cope H, Shashi V; Undiagnosed Diseases Network; Friedman J, Joset P, Steindl K, Rauch A, Muffels I, van Hasselt PM, Petit F, Smol T, Le Guyader G, Bilan F, Sorlin A, Vitobello A, Philippe C, van de Laar IMBH, van Slegtenhorst MA, Campeau PM, Au PYB, Nakashima M, Saitsu H, Yamamoto T, Nomura Y, Louie RJ, Lyons MJ, Dobson A, Plomp AS, Motazacker MM, Kaiser FJ, Timberlake AT, Fuchs SA, Depienne C, Mignot C (2021) Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy. Hum Genet 140(7):1109–1120. https://doi.org/10.1007/s00439-021-02283-2

Ferreira CR, Xia ZJ, Clément A, Parry DA, Davids M, Taylan F, Sharma P, Turgeon CT, Blanco-Sánchez B, Ng BG, Logan CV, Wolfe LA, Solomon BD, Cho MT, Douglas G, Carvalho DR, Bratke H, Haug MG, Phillips JB, Wegner J, Tiemeyer M, Aoki K (2018) A recurrent de novo heterozygous COG4 substitution leads to Saul-Wilson syndrome, disrupted vesicular trafficking, and altered proteoglycan glycosylation. Am J Hum Genet 103(4):553–567. https://doi.org/10.1016/j.ajhg.2018.09.003

Article  CAS  PubMed  PubMed Central 

留言 (0)

沒有登入
gif