Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: Syndrome and FOXP3[original query] |
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No association between variation of the FOXP3 gene and common type 1 diabetes in the Sardinian population. Diabetes 2004 Jul 53 (7): 1911-4. Zavattari Patrizia, Deidda Elisabetta, Pitzalis Maristella, Zoa Barbara, Moi Loredana, Lampis Rosanna, Contu Daniela, Motzo Costantino, Frongia Paola, Angius Efisio, Maioli Mario, Todd John A, Cucca Frances |
Autoimmune thyroiditis and diabetes: dissecting the joint genetic susceptibility in a large cohort of multiplex families. The Journal of clinical endocrinology and metabolism 2009 Apr 94 (4): 1458-66. Villano Maria Justina B, Huber Amanda K, Greenberg David A, Golden Brian K, Concepcion Erlinda, Tomer Yar |
[A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child]. Zhonghua er ke za zhi = Chinese journal of pediatrics 2010 1 47 (11): 824-8. An Yun-fei, Zhao Xiao-dong, Xu Feng, Yang Xi-qia |
FOXP3 genetic variant and risk of acute coronary syndrome in Chinese Han population. Cell biochemistry and function 2013 Oct 31 (7): 599-602. Yang Qing, Chen Yu, Yong W |
Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome. Scientific reports 2015 5 9511. Liao Dan, Hou Shengping, Zhang Jun, Fang Jing, Liu Yunjia, Bai Lin, Cao Qingfeng, Kijlstra Aize, Yang Peize |
Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome. Circulation. Cardiovascular genetics 2015 Dec . Sinisalo Juha, Vlachopoulou Efthymia, Marchesani Marja, Nokelainen Johanna, Mäyränpää Mikko I, Lappalainen Jani, Paakkanen Riitta, Wennerström Annika, Salli Krista, Niemi Heikki J, Männistö Satu, Salo Perttu, Junttila Juhani, Eskola Markku, Nikus Kjell, Arstila T Petteri, Perola Markus, Huikuri Heikki, Karhunen Pekka J, Kovanen Petri T, Palotie Aarno, Havulinna Aki S, Lluís-Ganella Carla, Marrugat Jaume, Elosua Roberto, Salomaa Veikko, Nieminen Markku S, Lokki Marja-Lii |
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells. The Journal of allergy and clinical immunology 2016 Jun . Chen Hannah H, Händel Norman, Ngeow Joanne, Muller James, Hühn Michael, Yang Huei-Ting, Heindl Mario, Berbers Roos-Marijn, Hegazy Ahmed N, Kionke Janina, Yehia Lamis, Sack Ulrich, Bläser Frank, Rensing-Ehl Anne, Reifenberger Julia, Keith Julia, Travis Simon, Merkenschlager Andreas, Kiess Wieland, Wittekind Christian, Walker Lisa, Ehl Stephan, Aretz Stefan, Dustin Michael L, Eng Charis, Powrie Fiona, Uhlig Holm |
Genetic variants and expression study of FOXP3 gene in acute coronary syndrome in Iranian patients. Cell biochemistry and function 2016 Apr 34 (3): 158-62. Gholami Milad, Esfandiary Ali, Vatanparast Masoumeh, Mirfakhraie Reza, Hosseini Mir Mohsen, Ghafouri-Fard Soud |
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: A systematic review. Autoimmunity reviews 2020 4 19 (6): 102526. Park Jae Hyon, Lee Keum Hwa, Jeon Bokyoung, Ochs Hans D, Lee Joon Suk, Gee Heon Yung, Seo Seeun, Geum Dongil, Piccirillo Ciriaco A, Eisenhut Michael, van der Vliet Hans J, Lee Jiwon M, Kronbichler Andreas, Ko Younhee, Shin Jae |
SNPs and transcriptional activity of genes of innate and adaptive immunity at the maternal-fetal interface in woman with preterm labour, associated with preterm premature rupture of membranes. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2020 73 (1): 25-30. Lyubomirskaya Ekaterina S, Kamyshnyi Alexandr M, Krut Yuriy Ya, Smiianov Vladyslav A, Fedoniuk Larisa Ya, Romanyuk Lidiya B, Kravets Natalya Ya, Mochulska Oksana |
The Relationship Between Serum Concentration of Interleukin-35 and FoxP3 Polymorphism in Patients Undergoing Coronary Artery Bypass Graft Surgery. Brazilian journal of cardiovascular surgery 2020 10 35 (5): 697-705. Dasturian Farzaneh, Naderi Nadereh, Farshidfar Gholamreza, Montazerghaem Hossein, Khayatian Mahmood, Chegeni Sara Aghakhani, Rahimzadeh Mah |
Impact of TNF-? Gene Polymorphisms on Pancreatic and Non-Small Cell Lung Cancer-Induced Cachexia in Adult Egyptian Patients: A Focus on Pathogenic Trajectories. Frontiers in oncology 2021 12 11 783231. Yehia Rana, Schaalan Mona, Abdallah Dalaal M, Saad Amr S, Sarhan Neven, Saleh Sami |
Analysis of selected polymorphisms in FOXP3 gene in a cohort of Egyptian patients with schizophrenia. Journal, genetic engineering & biotechnology 2022 5 20 (1): 83. Mostafa Maged, Fathy Aya Ahmed, Elwasify Mohamed, Abdelsalam Ma |
DNA Polymorphisms in Pregnant Women with Sticky Platelet Syndrome. Journal of clinical medicine 2022 11 11 (21): . Stan?iaková Lucia, Žolková Jana, Vadelová ?ubica, Hornáková Andrea, Kolková Zuzana, Vážan Martin, Dobrotová Miroslava, Hollý Pavol, Jedináková Zuzana, Grendár Marián, Bolek Tomáš, Samoš Matej, Biringer Kamil, Danko Ján, Burjanivová Tatiana, Lasabová Zora, Kubisz Peter, Staško J |
Autoimmune regulator (AIRE): Takes a hypoxia-inducing factor 1A (HIF1A) route to regulate FOXP3 expression in PCOS. American journal of reproductive immunology (New York, N.Y. : 1989) 2022 10 89 (2): e13637. Padmanabhan Renjini Ambika, Johnson Betcy Susan, Dhyani Ajay Kumar, Pillai Sathy M, Jayakrishnan K, Laloraya Mali |
FOXP3-positive cell infiltration in the chorionic villi is increased in the placenta accreta and decreased in the placental abruption. Ginekologia polska 2023 8 . Magdalena Dutsch-Wicherek, Blazej Nowakowski, Jan Faryna, Krystyna Galazka, Michal Lew-Starowicz, Sebastian Szube |
Immunophenotypic Alterations in Adult Patients with Steroid-Dependent and Frequently Relapsing Nephrotic Syndrome. International journal of molecular sciences 2023 5 24 (9): . Federica Casiraghi, Marta Todeschini, Manuel Alfredo Podestà, Marilena Mister, Barbara Ruggiero, Matias Trillini, Camillo Carrara, Olimpia Diadei, Alessandro Villa, Ariela Benigni, Giuseppe Remuz |
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