Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: CYP11B1[original query] |
---|
Characteristics of Japanese aldosterone-producing adenomas with KCNJ5 mutations. Endocrine journal 2016 Sep . Okamura Takashi, Nakajima Yasuyo, Katano-Toki Akiko, Horiguchi Kazuhiko, Matsumoto Shunichi, Yoshino Satoshi, Yamada Eijiro, Tomaru Takuya, Ishii Sumiyasu, Saito Tsugumichi, Ozawa Atsushi, Shibusawa Nobuyuki, Satoh Tetsurou, Okada Shuichi, Nagaoka Rin, Takada Daisuke, Horiguchi Jun, Oyama Tetsunari, Yamada Masano |
A polymorphism in the CYP17A1 gene influences the therapeutic response to steroidogenesis inhibitors in Cushing's syndrome. Clinical endocrinology 2017 Jun . Valassi Elena, Aulinas Anna, Glad Camilla Am, Johannsson Gudmundur, Ragnarsson Oskar, Webb Susan |
An exploratory study by DMET array identifies a germline signature associated with imatinib response in gastrointestinal stromal tumor. The pharmacogenomics journal 2019 Aug 19 (4): 390-400. Ravegnini Gloria, Urbini Milena, Simeon Vittorio, Genovese Chiara, Astolfi Annalisa, Nannini Margherita, Gatto Lidia, Saponara Maristella, Ianni Manuela, Indio Valentina, Brandi Giovanni, Trino Stefania, Hrelia Patrizia, Biasco Guido, Angelini Sabrina, Pantaleo Maria |
Aldosterone Suppression by Dexamethasone in Patients With KCNJ5-Mutated Aldosterone-Producing Adenoma. The Journal of clinical endocrinology and metabolism 2018 7 103 (9): 3477-3485. Inoue Kosuke, Yamazaki Yuto, Kitamoto Takumi, Hirose Rei, Saito Jun, Omura Masao, Sasano Hironobu, Nishikawa Tets |
Prevalence, clinical characteristics and long-term outcomes of classical 11 ?-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene. The Journal of steroid biochemistry and molecular biology 2018 4 181 88-97. Ba? Firdevs, Toksoy Güven, Ergun-Longmire Berrin, Uyguner Zehra Oya, Abal? Zehra Yava?, Poyrazo?lu ?ükran, Karaman Volkan, Avc? ?ahin, Altuno?lu Umut, Bundak Ruveyde, Karaman Birsen, Ba?aran Seher, Darendeliler Fey |
Giant bilateral adrenal myelolipomas in two Chinese families with congenital adrenal hyperplasia. Endocrine connections 2018 10 7 (11): 1136-41. Liu Qiuli, Wang Lin-Ang, Su Jian, Tong Dali, Lan Weihua, Wang Luofu, Liu Gaolei, Zhang Jun, Zhang Victor Wei, Zhang Dianzheng, Chen Rongrong, Zhu Qingyi, Jiang J |
Genetic Determinants of Circulating Estrogen Levels and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
The Journal of clinical endocrinology and metabolism 2018 Jan . Eriksson Anna L, Perry John R B, Coviello Andrea D, Delgado Graciela E, Ferrucci Luigi, Hoffman Andrew R, Huhtaniemi Ilpo T, Ikram M Arfan, Karlsson Magnus K, Kleber Marcus E, Laughlin Gail A, Liu Yongmei, Lorentzon Mattias, Lunetta Kathryn L, Mellström Dan, Murabito Joanne M, Murray Anna, Nethander Maria, Nielson Carrie M, Prokopenko Inga, Pye Stephen R, Raffel Leslie J, Rivadeneira Fernando, Srikanth Priya, Stolk Lisette, Teumer Alexander, Travison Thomas G, Uitterlinden André G, Vaidya Dhananjay, Vanderschueren Dirk, Zmuda Joseph M, März Winfried, Orwoll Eric S, Ouyang Pamela, Vandenput Liesbeth, Wu Frederick C W, de Jong Frank H, Bhasin Shalender, Kiel Douglas P, Ohlsson Cla |
In situ metabolomics of aldosterone-producing adenomas. JCI insight 2019 Sep 4 (17): . Murakami Masanori, Rhayem Yara, Kunzke Thomas, Sun Na, Feuchtinger Annette, Ludwig Philippe, Strom Tim Matthias, Gomez-Sanchez Celso, Knösel Thomas, Kirchner Thomas, Williams Tracy Ann, Reincke Martin, Walch Axel Karl, Beuschlein Fel |
Steroid metabolism gene variants and their genotype-phenotype correlations in Chinese early-onset hypertension patients. Hypertension research : official journal of the Japanese Society of Hypertension 2019 8 42 (10): 1536-1543. Qin Fang, Liu Kai, Zhang Ce, Sun Xiaolu, Zhang Yang, Wu Yajie, Ma Wenjun, Wang Wei, Wu Xueyi, Qin Ying, Zou Yubao, Zhou Xianliang, Jiang Xiongjing, Wu Haiying, Hui Rutai, Wang Jizheng, Zhang Huimin, Song L |
Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease.
The Journal of clinical endocrinology and metabolism 2019 Nov 104 (11): 5008-5023. Pott Janne, Bae Yoon Ju, Horn Katrin, Teren Andrej, Kühnapfel Andreas, Kirsten Holger, Ceglarek Uta, Loeffler Markus, Thiery Joachim, Kratzsch Jürgen, Scholz Mark |
Comprehensive genotyping of Turkish women with hirsutism. Journal of endocrinological investigation 2019 2 42 (9): 1077-1087. Polat S, Karaburgu S, Ünlühizarc? K, Dündar M, Özkul Y, Arslan Y K, Karaca Z, Kelestimur |
Identification of Genetic Factors Underlying the Association between Sodium Intake Habits and Hypertension Risk. Nutrients 2020 8 12 (9): . Kwon Yu-Jin, Kim Jung Oh, Park Jae-Min, Choi Ja-Eun, Park Da-Hyun, Song Youhyun, Kim Seong-Jin, Lee Ji-Won, Hong Kyung-W |
Pharmacogenetic study of ACE, AGT, CYP11B1, CYP11B2 and eNOS gene variants in hypertensive patients from Faisalabad, Pakistan. JPMA. The Journal of the Pakistan Medical Association 2020 Apr 70 (4): 624-629. Hussain Misbah, Bilal Ahmed, Awan Fazli Rab |
11?-Hydroxylase (CYP11B1) gene variants and new-onset depression in later life. Journal of psychiatry & neuroscience : JPN 2020 Nov 46 (1): 190177. Ancelin Marie-Laure, Norton Joanna, Ritchie Karen, Chaudieu Isabelle, Ryan Joan |
Intratumoral heterogeneity of the tumor cells based on in situ cortisol excess in cortisol-producing adenomas; ?An association among morphometry, genotype and cellular senescence?. The Journal of steroid biochemistry and molecular biology 2020 10 204 105764. Gao Xin, Yamazaki Yuto, Tezuka Yuta, Pieroni Jacopo, Ishii Kae, Atsumi Nanako, Ono Yoshikiyo, Omata Kei, Morimoto Ryo, Nakamura Yasuhiro, Satoh Fumitoshi, Sasano Hirono |
Investigation of the FSHR, CYP11, and INSR Mutations and Polymorphisms in Iranian Infertile Women with Polycystic Ovary Syndrome (PCOS). Reports of biochemistry & molecular biology 2021 5 9 (4): 470-477. Seyed Abutorabi Elaheh, Hossein Rashidi Batool, Irani Shiva, Haghollahi Fedyeh, Bagheri Mary |
Variable expression quantitative trait loci analysis of breast cancer risk variants. Scientific reports 2021 3 11 (1): 7192. Wiggins George A R, Black Michael A, Dunbier Anita, Merriman Tony R, Pearson John F, Walker Logan |
CYP11B1 variants influence skeletal maturation via alternative splicing.
Communications biology 2021 Nov 4 (1): 1274. Grgic Olja, Gazzara Matthew R, Chesi Alessandra, Medina-Gomez Carolina, Cousminer Diana L, Mitchell Jonathan A, Prijatelj Vid, de Vries Jard, Shevroja Enisa, McCormack Shana E, Kalkwarf Heidi J, Lappe Joan M, Gilsanz Vicente, Oberfield Sharon E, Shepherd John A, Kelly Andrea, Mahboubi Soroosh, Faucz Fabio R, Feelders Richard A, de Jong Frank H, Uitterlinden Andre G, Visser Jenny A, Ghanem Louis R, Wolvius Eppo B, Hofland Leo J, Stratakis Constantine A, Zemel Babette S, Barash Yoseph, Grant Struan F A, Rivadeneira Fernan |
Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India. European journal of medical genetics 2021 10 64 (12): 104369. Ravichandran Lavanya, Korula Sophy, Asha H S, Varghese Deny, Parthiban R , Johnson Jabasteen, Ishwarya Janani, Shetty Sahana, Cherian Kripa Elizabeth, Jebasingh Felix, Kapoor Nitin, Pachat Divya, Mathai Sarah, Simon Anna, Rajaratnam Simon, Paul Thomas V, Thomas Nihal, Chapla Aar |
Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease. BMC medical genomics 2022 Jul 15 (1): 158. Huang Xiaoli, Cheng Yimin, Wang |
Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal Hyperplasia. MethodsX 2022 6 9 101748. Ravichandran Lavanya, Varghese Deny, R Parthiban, S Asha H, Korula Sophy, Thomas Nihal, Chapla Aar |
Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read Sequencing. Clinical chemistry 2022 6 68 (7): 927-939. Liu Yingdi, Chen Miaomiao, Liu Jing, Mao Aiping, Teng Yanling, Yan Huiming, Zhu Huimin, Li Zhuo, Liang Desheng, Wu Lingqi |
Exploration of KCNJ5 Somatic Mutation and CYP11B1/CYP11B2 Staining in Multiple Nodules in Primary Aldosteronism. Frontiers in medicine 2022 9 823065. Xie Jing, Zhang Cui, Wang Xuefeng, Jiang Yiran, Wu Luming, Ye Lei, Wang Xuan, Xie Wen, Xu Haimin, Wang Weiqi |
CYP11B1 gene polymorphisms and susceptibility to ischemic stroke in a Chinese Han population. Frontiers in neuroscience 2022 12 16 1030551. Liu Gaowen, Duan Yi |
Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor. European journal of medical genetics 2022 11 65 (12): 104654. Aycan Zehra, Keskin Melik?ah, Lafc? Naz Güleray, Sava?-Erdeve ?enay, Ba? Firdevs, Poyrazo?lu ?ükran, Öztürk P?nar, Parlak Mesut, Ercan Oya, Güran Tülay, Hatipo?lu Nihal, Uçaktürk Seyit Ahmet, Çatl? Gönül, Akyürek Nesibe, Önder A?an, K?l?nç Suna, Çetinkaya Sem |
Association between Germline Single-Nucleotide Variants in ADME Genes and Major Molecular Response to Imatinib in Chronic Myeloid Leukemia Patients. Journal of clinical medicine 2022 10 11 (20): . Estrada Natalia, Zamora Lurdes, Ferrer-Marín Francisca, Palomo Laura, García Olga, Vélez Patricia, De la Fuente Iris, Sagüés Miguel, Cabezón Marta, Cortés Montserrat, Vallansot Rolando Omar, Senín-Magán María Alicia, Boqué Concepción, Xicoy Blan |
Cytogenetic and molecular insight into the genetic background of disorders of sex development in seventeen cats. Scientific reports 2022 10 12 (1): 17807. Stachowiak Monika, Szczerbal Izabela, Nowacka-Woszuk Joanna, Nowak Tomasz, Sowinska Natalia, Lukomska Anna, Gogulski Maciej, Badura Malgorzata, Sklorz-Mencel Karolina, Jagodka Dariusz, Nizanski Wojciech, Dzimira Stanislaw, Switonski Mar |
Association Between the Polymorphism of Steroid Hormone Metabolism Genes and High-Altitude Pulmonary Edema in the Chinese Han Population. International journal of general medicine 2022 15 787-794. Gao Hui, Xu Jin, Ma Qiang, Tang Feng, Ga Qin, Li Yuhong, Guan Wei, Ge Ri-Li, Yang Ying-Zho |
Serum Androgen Metabolites Correlate with Clinical Variables in African and European American Men with Localized, Therapy Naïve Prostate Cancer. Metabolites 2023 2 13 (2): . Ramakrishnan Swathi, Kittles Rick A, Huss Wendy J, Wang Jianmin, Attwood Kristopher, Woloszynska An |
A common germline variant in CYP11B1 is associated with adverse clinical outcome of treatment with abiraterone or enzalutamide. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2023 11 169 115890. Stefan A J Buck, Marinda Meertens, Frederiek M F van Ooijen, Esther Oomen-de Hoop, Evert de Jonge, Marieke J H Coenen, Andries M Bergman, Stijn L W Koolen, Ronald de Wit, Alwin D R Huitema, Ron H N van Schaik, Ron H J Mathijss |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: