Assessment of the Potential Role of Selected Single Nucleotide Polymorphisms (SNPs) of Genes Related to the Functioning of Regulatory T Cells in the Pathogenesis of Psoriasis.
International Journal Of Molecular Sciences
Purzycka-Bohdan, Dorota D; Nedoszytko, Bogusław B; Sobalska-Kwapis, Marta M; Zabłotna, Monika M; Żmijewski, Michał A MA; Wierzbicka, Justyna J; Gleń, Jolanta J; Strapagiel, Dominik D; Szczerkowska-Dobosz, Aneta A; Nowicki, Roman J RJ
Forkhead box P3 gene polymorphisms predispose to type 2 diabetes and diabetic nephropathy in the Han Chinese populations: a genetic-association and gender-based evaluation study.
Pre-Existing Diabetes Mellitus, Hypertension and KidneyDisease as Risk Factors of Pre-Eclampsia: A Disease of Theories and Its Association with Genetic Polymorphism.
International Journal Of Environmental Research And Public Health
Alanazi, Abdullah Salah AS; Victor, Francis F; Rehman, Kanwal K; Khan, Yusra Habib YH; Yunusa, Ismaeel I; Alzarea, Abdulaziz Ibrahim AI; Akash, Muhammad Sajid Hamid MSH; Mallhi, Tauqeer Hussain TH
Anti-Thymocyte Globulin (ATG)-Free Nonmyeloablative Haploidentical PBSCT Plus Post-Transplantation Cyclophosphamide Is a Safe and Efficient Treatment Approach for Pediatric Acquired Aplastic Anemia.
DNA Polymorphisms in Pregnant Women with Sticky Platelet Syndrome.
Journal Of Clinical Medicine
Stančiaková, Lucia L; Žolková, Jana J; Vadelová, Ľubica Ľ; Hornáková, Andrea A; Kolková, Zuzana Z; Vážan, Martin M; Dobrotová, Miroslava M; Hollý, Pavol P; Jedináková, Zuzana Z; Grendár, Marián M; Bolek, Tomáš T; Samoš, Matej M; Biringer, Kamil K; Danko, Ján J; Burjanivová, Tatiana T; Lasabová, Zora Z; Kubisz, Peter P; Staško, Ján J
LncRNA-miRNA network analysis across the Th17 cell line reveals biomarker potency of lncRNA NEAT1 and KCNQ1OT1 in multiple sclerosis.
Journal Of Cellular And Molecular Medicine
Karimi, Elham E; Azari, Hanieh H; Tahmasebi, Ahmad A; Nikpoor, Amin Reza AR; Negahi, Ahmad Agha AA; Sanadgol, Nima N; Shekari, Mohammad M; Mousavi, Pegah P
A systematic review of common genetic variation and biological pathways in autism spectrum disorder.
Bmc Neuroscience
Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C
FOXP3 and GATA3 Polymorphisms, Vitamin D3 and Multiple Sclerosis.
Brain Sciences
Scazzone, Concetta C; Agnello, Luisa L; Lo Sasso, Bruna B; Salemi, Giuseppe G; Gambino, Caterina Maria CM; Ragonese, Paolo P; Candore, Giuseppina G; Ciaccio, Anna Maria AM; Giglio, Rosaria Vincenza RV; Bivona, Giulia G; Vidali, Matteo M; Ciaccio, Marcello M
Polymorphisms in the TGFB1 and FOXP3 genes are associated with the presence of antinuclear antibodies in chronic hepatitis C.
Heliyon
de Castro, Geison Luiz Costa GLC; Bichara, Carlos David A CDA; Santiago, Angélica Menezes AM; de Brito, William Botelho WB; Pereira, Leonn Mendes Soares LMS; Moura, Tuane Carolina Ferreira TCF; da Silva Graça Amoras, Ednelza E; de Araújo, Mauro Sérgio Moura MSM; da Silva Conde, Simone Regina Souza SRS; Queiroz, Maria Alice Freitas MAF; Ishak, Ricardo R; Vallinoto, Antonio Carlos Rosário ACR
Pathogenesis of psoriasis in the "omic" era. Part I. Epidemiology, clinical manifestation, immunological and neuroendocrine disturbances.
Postepy Dermatologii I Alergologii
Samotij, Dominik D; Nedoszytko, Bogusław B; Bartosińska, Joanna J; Batycka-Baran, Aleksandra A; Czajkowski, Rafał R; Dobrucki, Iwona T IT; Dobrucki, Lawrence W LW; Górecka-Sokołowska, Magdalena M; Janaszak-Jasienicka, Anna A; Krasowska, Dorota D; Kalinowski, Leszek L; Macieja-Stawczyk, Marta M; Nowicki, Roman J RJ; Owczarczyk-Saczonek, Agnieszka A; Płoska, Agata A; Purzycka-Bohdan, Dorota D; Radulska, Adrianna A; Reszka, Edyta E; Siekierzycka, Anna A; Słomiński, Andrzej A; Słomiński, Radomir R; Sobalska-Kwapis, Marta M; Strapagiel, Dominik D; Szczerkowska-Dobosz, Aneta A; Szczęch, Justyna J; Żmijewski, Michał M; Reich, Adam A
Transcription factor FOXP3 gene variants affect epithelial ovarian carcinoma in the Han Chinese population.
International Journal Of Clinical And Experimental Pathology
Zhang, Yan Y; Xu, Lian L; Zhou, Bin B; Li, Qin Q; You, Di D; Liu, Chenlu C; Song, Huizi H; Wang, Yanyun Y; Song, Yaping Y; Su, Min M; Huang, Xingming X; Yuan, Mingwei M; Lan, Zhu Z; Wang, Wei W
Identification of genetic variants associated with tacrolimus metabolism in kidney transplant recipients by extreme phenotype sampling and next generation sequencing.
The Pharmacogenomics Journal
Dorr, Casey R CR; Wu, Baolin B; Remmel, Rory P RP; Muthusamy, Amutha A; Schladt, David P DP; Abrahante, Juan E JE; Guan, Weihua W; Mannon, Roslyn B RB; Matas, Arthur J AJ; Oetting, William S WS; Jacobson, Pamala A PA; Israni, Ajay K AK; ,