Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 32 Records) |
| Query Trace: Syndrome and NR3C1[original query] |
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| Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome. Biochemical and biophysical research communications 2006 Sep 348 (2): 507-13. Ye Jianwei, Yu Zihua, Ding Jie, Chen Yan, Huang Jianping, Yao Yong, Xiao Huijie, Yang Jiyun, Shen Ying, Meng Q |
| Glucocorticoid receptor polymorphisms and haplotypes associated with chronic fatigue syndrome. Genes, brain, and behavior 2007 Mar 6 (2): 167-76. Rajeevan M S, Smith A K, Dimulescu I, Unger E R, Vernon S D, Heim C, Reeves W |
| Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue. Pharmacogenomics 2006 Apr 7 (3): 387-94. Smith Alicia K, White Peter D, Aslakson Eric, Vollmer-Conna Ute, Rajeevan Mangalathu |
| Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome. Pharmacogenomics 2006 Apr 7 (3): 475-83. Goertzel Benjamin N, Pennachin Cassio, de Souza Coelho Lucio, Gurbaxani Brian, Maloney Elizabeth M, Jones James |
| Response to prednisone in relation to NR3C1 intron B polymorphisms in childhood nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2008 Jul 23 (7): 1073-8. Zalewski Grzegorz, Wasilewska Anna, Zoch-Zwierz Walentyna, Chyczewski Le |
| A Bayesian approach to gene-gene and gene-environment interactions in chronic fatigue syndrome. Pharmacogenomics 2009 Jan 10 (1): 35-42. Lin Eugene, Hsu Sen-Y |
| Glutathione-S-transferase-P1 I105V polymorphism and response to antenatal betamethasone in the prevention of respiratory distress syndrome. European journal of clinical pharmacology 2009 May 65 (5): 483-91. Oretti Chiara, Marino Sara, Mosca Fabio, Colnaghi Maria Rosa, De Iudicibus Sara, Drigo Ilenia, Stocco Gabriele, Bartoli Fiora, Decorti Giuliana, Demarini Serg |
| Association of glucocorticoid receptor polymorphism A3669G with decreased risk of developing diabetes in patients with Cushing's syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2012 Jan 166 (1): 35-42. Trementino Laura, Appolloni Gloria, Concettoni Carolina, Cardinaletti Marina, Boscaro Marco, Arnaldi Giorg |
| BClI polymorphism of the glucocorticoid receptor gene is associated with increased obesity, impaired glucose metabolism and dyslipidaemia in patients with Addison's disease. Clinical endocrinology 2012 Dec 77 (6): 863-70. Giordano Roberta, Marzotti Stefania, Berardelli Rita, Karamouzis Ioannis, Brozzetti Annalisa, D'Angelo Valentina, Mengozzi Giulio, Mandrile Giorgia, Giachino Daniela, Migliaretti Giuseppe, Bini Vittorio, Falorni Alberto, Ghigo Ezio, Arvat Emanue |
| Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency. PloS one 2012 7 (9): 9. Moreira RP, Gomes LG, Mendonca BB, Bachega TA |
| Polymorphisms in NR3C1 gene associated with risk of metabolic syndrome in a Chinese population. Endocrine 2014 Dec 47 (3): 740-8. Yan Yu-Xiang, Dong Jing, Zhang Jie, Liu Fen, Wang Wei, Zhang Ling, He Y |
| Common genetic variants in the glucocorticoid receptor and the 11ß-hydroxysteroid dehydrogenase type 1 genes influence long-term cognitive impairments in patients with Cushing's syndrome in remission. The Journal of clinical endocrinology and metabolism 2014 Sep 99 (9): E1803-7. Ragnarsson Oskar, Glad Camilla A M, Berglund Peter, Bergthorsdottir Ragnhildur, Eder Derek N, Johannsson Gudmund |
| Association of glucocorticoid receptor polymorphisms with clinical and metabolic profiles in polycystic ovary syndrome. Clinics (São Paulo, Brazil) 2014 Mar 69 (3): 179-84. Maciel Gustavo A Rosa, Moreira Ricardo P P, Bugano Diogo D G, Hayashida Sylvia A Y, Marcondes José A M, Gomes Larissa G, Mendonça Berenice B, Bachega Tânia A S S, Baracat Edmund |
| Body composition and bone mineral density in women with Cushing's syndrome in remission and the association with common genetic variants influencing glucocorticoid sensitivity. European journal of endocrinology / European Federation of Endocrine Societies 2015 Jan 172 (1): 1-10. Ragnarsson Oskar, Glad Camilla A M, Bergthorsdottir Ragnhildur, Almqvist Erik G, Ekerstad Eva, Widell Håkan, Wängberg Bo, Johannsson Gudmund |
| Impact of glucocorticoid receptor gene (NR3C1) polymorphisms in Turkish patients with metabolic syndrome. Journal of endocrinological investigation 2015 Nov . Kaya Z, Caglayan S, Akkiprik M, Aral C, Ozisik G, Ozata M, Ozer |
| Interactions of early adversity with stress-related gene polymorphisms impact regional brain structure in females. Brain structure & function 2015 Jan . Gupta Arpana, Labus Jennifer, Kilpatrick Lisa A, Bonyadi Mariam, Ashe-McNalley Cody, Heendeniya Nuwanthi, Bradesi Sylvie, Chang Lin, Mayer Emeran |
| Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome. International journal of nephrology 2016 2016 1417456. Suvanto Maija, Jahnukainen Timo, Kestilä Marjo, Jalanko Han |
| HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome. Diabetes/metabolism research and reviews 2016 Aug . Martins Clarissa Silva, Elias Daniel, Colli Leandro Machado, Couri Carlos Eduardo, Souza Manoel Carlos L A, Moreira Ayrton C, Foss Milton C, Elias Lucila L K, de Castro Margar |
| Decreased comfort food intake and allostatic load in adolescents carrying the A3669G variant of the glucocorticoid receptor gene. Appetite 2017 Apr . Rodrigues Danitsa Marcos, Reis Roberta Sena, Dalle Molle Roberta, Machado Tania Diniz, Mucellini Amanda Brondani, Bortoluzzi Andressa, Toazza Rudineia, Pérez Juliano Adams, Salum Giovanni Abrahão, Agranonik Marilyn, Minuzzi Luciano, Levitan Robert D, Buchweitz Augusto, Franco Alexandre Rosa, Manfro Gisele Gus, Silveira Patrícia Pelu |
| NR3C1 gene polymorphisms are associated with steroid resistance in patients with primary nephrotic syndrome. Pharmacogenomics 2017 Dec . Liu Jie, Wan Zan, Song Qianqian, Li Zhi, He Yijing, Tang Yongjun, Xie Wanying, Xie Yanyun, Zhang J |
| A systematic review of the association between fatigue and genetic polymorphisms. Brain, behavior, and immunity 2017 1 62 230-244. Wang Tengteng, Yin Jie, Miller Andrew H, Xiao Canh |
| A Novel Pathogenic Variant in the N-Terminal Domain of the Glucocorticoid Receptor, Causing Glucocorticoid Resistance. Molecular diagnosis & therapy 2020 7 24 (4): 473-485. Paragliola Rosa Maria, Costella Alessandra, Corsello Andrea, Urbani Andrea, Concolino Pao |
| Glucocorticoid regulation and neuroanatomy in fragile x syndrome. Journal of psychiatric research 2020 Dec 134 81-88. Bruno Jennifer L, Hong David S, Lightbody Amy A, Hosseini S M Hadi, Hallmayer Joachim, Reiss Allan |
| Pituitary dysmaturation affects psychopathology and neurodevelopment in 22q11.2 Deletion Syndrome. Psychoneuroendocrinology 2020 1 113 104540. Sandini Corrado, Chambaz Maëlle, Schneider Maude, Armando Marco, Zöller Daniela, Schaer Marie, Sandi Carmen, Van De Ville Dimitri, Eliez Steph |
| Children with Down syndrome: association of Bcl-I polymorphism of nuclear receptor subfamily 3 group C member 1 gene with obesity. Pediatric research 2021 8 92 (1): 216-224. Abo El-Fotoh Wafaa Moustafa M, Bahbah Hebatallah Mohammed Nasser, Elaithy Manal Abd El-Monem, Ahmed Rana Khairy Rashad, Bayomy Noha Rab |
| Untargeted Plasma Metabolomics Unravels a Metabolic Signature for Tissue Sensitivity to Glucocorticoids in Healthy Subjects: Its Implications in Dietary Planning for a Healthy Lifestyle. Nutrients 2021 7 13 (6): . Nicolaides Nicolas C, Ioannidi Maria-Konstantina, Koniari Eleni, Papageorgiou Ifigeneia, Bartzeliotou Anastasia, Sertedaki Amalia, Klapa Maria I, Charmandari Evangel |
| Assessment of the Link of ABCB1 and NR3C1 gene polymorphisms with the prednisolone resistance in pediatric nephrotic syndrome patients of Bangladesh: A genotype and haplotype approach. Journal of advanced research 2021 Nov 33 141-151. Parvin Most Nazma, Aziz Md Abdul, Rabbi Sikder Nahidul Islam, Al-Mamun Mir Md Abdullah, Hanif Mohammed, Islam Md Saiful, Islam Mohammad Safiq |
| Clinicopathological Impact of Gene Polymorphism of Nephrin and Glucocorticoid Receptor Genes in Egyptian Children with Nonfamilial Nephrotic Syndrome. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 0 32 (6): 1615-1627. El-Refaey Ahmed M, Elsamanoudy Ayman Z, Elmorsy Zakarya, Gaber Eman, Sarhan Amr, Hammad Aymman, Zedan Mohamed M, Bakr Ashr |
| SFTPB (rs11130866) and NR3C1 (rs41423247) gene variants as potential clinical biomarkers for personalized treatment strategy selection in patients with severe COVID-19 pneumonia. Respiratory investigation 2022 12 61 (1): 103-109. Fishchuk Liliia, Rossokha Zoia, Pokhylko Valeriy, Cherniavska Yuliia, Popova Olena, Vershyhora Viktoriia, Kovtun Serhii, Gorovenko Natali |
| Familial Linkage and Association of the NR3C1 Gene with Type 2 Diabetes and Depression Comorbidity. International journal of molecular sciences 2022 10 23 (19): . Amin Mutaz, Syed Shumail, Wu Rongling, Postolache Teodor Tudorel, Gragnoli Claud |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
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