Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: HSD11B2[original query] |
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Association studies between the HSD11B2 gene (encoding human 11beta-hydroxysteroid dehydrogenase type 2), type 1 diabetes mellitus and diabetic nephropathy. European journal of endocrinology / European Federation of Endocrine Societies 2002 Apr 146 (4): 553-8. Lavery Gareth G, McTernan Claire L, Bain Stephen C, Chowdhury Tahseen A, Hewison Martin, Stewart Paul |
Genetic analysis of 22 candidate genes for hypertension in the Japanese population. Journal of hypertension 2004 Jun 22 (6): 1119-26. Iwai Naoharu, Tago Naomi, Yasui Naomi, Kokubo Yoshihiro, Inamoto Nozomu, Tomoike Hitonobu, Shioji Keisu |
Analysis of the 11beta-hydroxysteroid dehydrogenase type 2 gene (HSD11B2) in human essential hypertension. American journal of hypertension 2005 Aug 18 (8): 1091-8. Mariniello Barbara, Ronconi Vanessa, Sardu Cipriana, Pagliericcio Antonella, Galletti Ferruccio, Strazzullo Pasquale, Palermo Mario, Boscaro Marco, Stewart Paul M, Mantero Franco, Giacchetti Gilber |
Role of HSD11B2 polymorphisms in essential hypertension and the diuretic response to thiazides. Kidney international 2005 Feb 67 (2): 631-7. Williams Tracy A, Mulatero Paolo, Filigheddu Fabiana, Troffa Chiara, Milan Alberto, Argiolas Giuseppe, Parpaglia Paolo Pinna, Veglio Franco, Glorioso Nico |
Biochemical and genetic characterization of 11 beta-hydroxysteroid dehydrogenase type 2 in low-renin essential hypertensives. Journal of hypertension 2005 1 23 (1): 71-7. Carvajal Cristian A, Romero Damián G, Mosso Lorena M, González Alexis A, Campino Carmen, Montero Joaquín, Fardella Carlos |
Genetic variations of HSD11B2 in hypertensive patients and in the general population, six rare missense/frameshift mutations. Hypertension research : official journal of the Japanese Society of Hypertension 2006 Apr 29 (4): 243-52. Kamide Kei, Kokubo Yoshihiro, Hanada Hironori, Nagura Junko, Yang Jin, Takiuchi Shin, Tanaka Chihiro, Banno Mariko, Miwa Yoshikazu, Yoshii Masayoshi, Matayoshi Tetsutaro, Yasuda Hisayo, Horio Takeshi, Okayama Akira, Tomoike Hitonobu, Kawano Yuhei, Miyata Toshiyu |
Identification of polymorphisms in the human 11beta-hydroxysteroid dehydrogenase type 2 gene promoter: functional characterization and relevance for salt sensitivity. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007 Nov 21 (13): 3618-28. Alikhani-Koupaei Rasoul, Fouladkou Fatemeh, Fustier Pierre, Cenni Bruno, Sharma Arya M, Deter Hans-Christian, Frey Brigitte M, Frey Felix |
SRD5A2 is associated with increased cortisol metabolism in schizophrenia spectrum disorders. Progress in neuro-psychopharmacology & biological psychiatry 2010 Dec 34 (8): 1500-6. Steen Nils Eiel, Tesli Martin, Kähler Anna K, Methlie Paal, Hope Sigrun, Barrett Elizabeth A, Larsson Sara, Mork Erlend, Løvås Kristian, Røssberg Jan Ivar, Agartz Ingrid, Melle Ingrid, Djurovic Srdjan, Lorentzen Steinar, Berg Jens P, Andreassen Ole |
Genetic variants in the renin-angiotensin-aldosterone system and blood pressure responses to potassium intake. Journal of hypertension 2011 Sep 29 (9): 1719-30. He Jiang, Gu Dongfeng, Kelly Tanika N, Hixson James E, Rao Dabeeru C, Jaquish Cashell E, Chen Jing, Zhao Qi, Gu Chi, Huang Jianfeng, Shimmin Lawrence C, Chen Ji-Chun, Mu Jianjun, Ji Xu, Liu De-Pei, Whelton Paul K, |
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation research 2012 Nov . Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freeman BI, Coresh J, Kao LW, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A |
11ß-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohort. American journal of hypertension 2012 May 25 (5): 597-603. Campino Carmen, Quinteros Hector, Owen Gareth I, Carvajal Cristian A, Morales Mauricio, Olivieri Oliviero, Guidi Giancesare, Faccini Giovanni, Pasini Francesco, Baudrand Rene, Padilla Oslando, Valdivia Carolina, Thichauer Juan, Lagos Carlos F, Kalergis Alexis M, Fardella Carlos |
Glucocorticoid synthesis-related genes: HSD11B1 and HSD11B2 in hypertensive disorders in pregnancy. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2013 Jul 29 (7): 657-61. Shimodaira Masanori, Nakayama Tomohiro, Sato Ichiro, Sato Naoyuki, Izawa Noriko, Mizutani Yoshihiro, Furuya Kiyohide, Yamamoto Tats |
Genetic polymorphisms in 11ß-hydroxysteroid dehydrogenase type 1 correlate with the postdexamethasone cortisol levels and bone mineral density in patients evaluated for osteoporosis. The Journal of clinical endocrinology and metabolism 2014 Feb 99 (2): E293-302. Siggelkow Heide, Etmanski Michael, Bozkurt Sarayi, Gro? Parissa, Koepp Regine, Brockmöller Jürgen, Tzvetkov Mladen |
Longer HSD11B2 CA-repeat in impaired glucose tolerance and type 2 diabetes. Endocrine journal 2013 60 (5): 671-8. Mune Tomoatsu, Suwa Tetsuya, Morita Hiroyuki, Isomura Yukinori, Takada Nobuki, Yamamoto Yoritsuna, Hayashi Makoto, Yamakita Noriyoshi, Sasaki Akihiko, Takeda Noriyuki, Takeda Jun, White Perrin C, Kaku Koh |
11ß-Hydroxysteroid dehydrogenase type 2 in hypertension: comparison of phenotype and genotype analysis. Journal of human hypertension 2013 Aug 27 (8): 510-5. Kosicka K, Cymerys M, Majchrzak-Celi?ska A, Chuchracki M, G?ówka F |
[Association between HSD11B2 gene polymorphism and fetal growth]. Nan fang yi ke da xue xue bao = Journal of Southern Medical University 2014 Aug 34 (9): 1286-90. Li Jian, Wang Zineng, Dong Yunpeng, Chen Dan, Chen Youpeng, Lu Yongping, Hocher Bertho |
Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia. Psychoneuroendocrinology 2015 Oct 60 18-27. Debost Jean-Christophe, Petersen Liselotte, Grove Jakob, Hedemand Anne, Khashan Ali, Henriksen Tine, Mors Ole, Hollegaard Mads, Hougaard David, Nyegaard Mette, Børglum Anders, Mortensen Preben |
Variants of HSD11B2 gene in hypertensive disorders of pregnancy. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2016 Aug 1-6. Kosicka Katarzyna, Siemi?tkowska Anna, P?kal Agnieszka, Majchrzak-Celi?ska Aleksandra, Br?borowicz Grzegorz, Krzy?cin Mariola, G?ówka Francisz |
Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients. Journal of hypertension 2017 Sep . Liu Kai, Qin Fang, Sun Xiaolu, Zhang Yang, Wang Jizheng, Wu Yajie, Ma Wenjun, Wang Wei, Wu Xueyi, Qin Ying, Zhang Huimin, Zhou Xianliang, Wu Haiying, Hui Rutai, Zou Yubao, Jiang Xiongjing, Song L |
Prednisolone and Prednisone Pharmacokinetics in Pediatric Renal Transplant Recipients-A Prospective Study. Therapeutic drug monitoring 2017 7 39 (5): 472-482. Skauby Ragnhild Heier, Bjerre Anna, Sæves Ingjerd, Vethe Nils Tore, Bremer Sara, Svarstad Anja, Bergan Ste |
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
![]() PLoS genetics 2017 Apr 13 (4): e1006719. Ng Maggie C Y, Graff Mariaelisa, Lu Yingchang, Justice Anne E, Mudgal Poorva, Liu Ching-Ti, Young Kristin, Yanek Lisa R, Feitosa Mary F, Wojczynski Mary K, Rand Kristin, Brody Jennifer A, Cade Brian E, Dimitrov Latchezar, Duan Qing, Guo Xiuqing, Lange Leslie A, Nalls Michael A, Okut Hayrettin, Tajuddin Salman M, Tayo Bamidele O, Vedantam Sailaja, Bradfield Jonathan P, Chen Guanjie, Chen Wei-Min, Chesi Alessandra, Irvin Marguerite R, Padhukasahasram Badri, Smith Jennifer A, Zheng Wei, Allison Matthew A, Ambrosone Christine B, Bandera Elisa V, Bartz Traci M, Berndt Sonja I, Bernstein Leslie, Blot William J, Bottinger Erwin P, Carpten John, Chanock Stephen J, Chen Yii-Der Ida, Conti David V, Cooper Richard S, Fornage Myriam, Freedman Barry I, Garcia Melissa, Goodman Phyllis J, Hsu Yu-Han H, Hu Jennifer, Huff Chad D, Ingles Sue A, John Esther M, Kittles Rick, Klein Eric, Li Jin, McKnight Barbara, Nayak Uma, Nemesure Barbara, Ogunniyi Adesola, Olshan Andrew, Press Michael F, Rohde Rebecca, Rybicki Benjamin A, Salako Babatunde, Sanderson Maureen, Shao Yaming, Siscovick David S, Stanford Janet L, Stevens Victoria L, Stram Alex, Strom Sara S, Vaidya Dhananjay, Witte John S, Yao Jie, Zhu Xiaofeng, Ziegler Regina G, Zonderman Alan B, Adeyemo Adebowale, Ambs Stefan, Cushman Mary, Faul Jessica D, Hakonarson Hakon, Levin Albert M, Nathanson Katherine L, Ware Erin B, Weir David R, Zhao Wei, Zhi Degui, , Arnett Donna K, Grant Struan F A, Kardia Sharon L R, Oloapde Olufunmilayo I, Rao D C, Rotimi Charles N, Sale Michele M, Williams L Keoki, Zemel Babette S, Becker Diane M, Borecki Ingrid B, Evans Michele K, Harris Tamara B, Hirschhorn Joel N, Li Yun, Patel Sanjay R, Psaty Bruce M, Rotter Jerome I, Wilson James G, Bowden Donald W, Cupples L Adrienne, Haiman Christopher A, Loos Ruth J F, North Kari |
Are genetic polymorphisms in the renin-angiotensin-aldosterone system associated with essential hypertension? Evidence from genome-wide association studies. Journal of human hypertension 2017 Apr . Ji L-D, Li J-Y, Yao B-B, Cai X-B, Shen Q-J, Xu |
Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11?-hydroxysteroid dehydrogenase type 2 deficiency. Proceedings of the National Academy of Sciences of the United States of America 2017 12 114 (52): E11248-E11256. Yau Mabel, Haider Shozeb, Khattab Ahmed, Ling Chen, Mathew Mehr, Zaidi Samir, Bloch Madison, Patel Monica, Ewert Sinead, Abdullah Wafa, Toygar Aysenur, Mudryi Vitalii, Al Badi Maryam, Alzubdi Mouch, Wilson Robert C, Al Azkawi Hanan Said, Ozdemir Hatice Nur, Abu-Amer Wahid, Hertecant Jozef, Razzaghy-Azar Maryam, Funder John W, Al Senani Aisha, Sun Li, Kim Se-Min, Yuen Tony, Zaidi Mone, New Maria |
Clinical, Biochemical, and Genetic Characteristics of "Nonclassic" Apparent Mineralocorticoid Excess Syndrome. The Journal of clinical endocrinology and metabolism 2018 9 104 (2): 595-603. Tapia-Castillo Alejandra, Baudrand Rene, Vaidya Anand, Campino Carmen, Allende Fidel, Valdivia Carolina, Vecchiola Andrea, Lagos Carlos F, Fuentes Cristóbal A, Solari Sandra, Martínez-Aguayo Alejandro, García Hernán, Carvajal Cristian A, Fardella Carlos |
Genomic imbalances in the placenta are associated with poor fetal growth. Molecular medicine (Cambridge, Mass.) 2021 1 27 (1): 3. Del Gobbo Giulia F, Yin Yue, Choufani Sanaa, Butcher Emma A, Wei John, Rajcan-Separovic Evica, Bos Hayley, von Dadelszen Peter, Weksberg Rosanna, Robinson Wendy P, Yuen Ryan K |
Atypical haemolytic uraemic syndrome in the era of terminal complement inhibition- An observational cohort study. Blood 2023 6 . Vicky Brocklebank, Patrick R Walsh, Kate Smith-Jackson, Thomas M Hallam, Kevin J Marchbank, Valerie Wilson, Theophile Bigirumurame, Tina Dutt, Emma K Montgomery, Michal Malina, Edwin Ks Wong, Sally Johnson, Neil Sheerin, David Kavana |
Predisposing factors for adrenal crisis in chronic adrenal insufficiency: a case-control study. European journal of endocrinology 2023 11 189 (5): 537-545. Irina Chifu, Stephanie Burger-Stritt, Anna Schrader, Sabine Herterich, Janik Freytag, Max Kurlbaum, Nora Vogg, Johanna Werner, Marcus Quinkler, Stefanie Hahn |
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- Page last updated:Jun 24, 2024
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