Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: PROK2[original query] |
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Genome-wide association of sleep and circadian phenotypes.
BMC medical genetics 2007 8 Suppl 1 S9. Gottlieb Daniel J, O'Connor George T, Wilk Jemma |
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. The Journal of clinical endocrinology and metabolism 2008 Oct 93 (10): 4113-8. Abreu Ana Paula, Trarbach Ericka Barbosa, de Castro Margaret, Frade Costa Elaine Maria, Versiani Beatriz, Matias Baptista Maria Tereza, Garmes Heraldo Mendes, Mendonca Berenice Bilharinho, Latronico Ana Claud |
Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1. Journal of andrology 0 30 (1): 41-5. Canto P, Munguía P, Söderlund D, Castro J J, Méndez J |
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome. Clinical genetics 2009 Jan 75 (1): 65-71. Jongmans M C J, van Ravenswaaij-Arts C M A, Pitteloud N, Ogata T, Sato N, Claahsen-van der Grinten H L, van der Donk K, Seminara S, Bergman J E H, Brunner H G, Crowley W F, Hoefsloot L |
A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes. The Journal of clinical endocrinology and metabolism 2010 Feb 95 (2): 659-69. Sarfati Julie, Guiochon-Mantel Anne, Rondard Philippe, Arnulf Isabelle, Garcia-Piñero Alfons, Wolczynski Slawomir, Brailly-Tabard Sylvie, Bidet Maud, Ramos-Arroyo Maria, Mathieu Michèle, Lienhardt-Roussie Anne, Morgan Graeme, Turki Zinet, Bremont Catherine, Lespinasse James, Du Boullay Hélène, Chabbert-Buffet Nathalie, Jacquemont Sébastien, Reach Gérard, De Talence Nicole, Tonella Paolo, Conrad Bernard, Despert Francois, Delobel Bruno, Brue Thierry, Bouvattier Claire, Cabrol Sylvie, Pugeat Michel, Murat Arnaud, Bouchard Philippe, Hardelin Jean-Pierre, Dodé Catherine, Young Jacqu |
Lack of association between prokineticin 2 gene and Japanese methamphetamine dependence. Current neuropharmacology 2011 Mar 9 (1): 133-6. Kishi Taro, Kitajima Tsuyoshi, Tsunoka Tomoko, Okumura Takenori, Kawashima Kunihiro, Okochi Tomo, Yamanouchi Yoshio, Kinoshita Yoko, Ujike Hiroshi, Inada Toshiya, Yamada Mitsuhiko, Uchimura Naohisa, Sora Ichiro, Iyo Masaomi, Ozaki Norio, Iwata Nak |
Isolated cryptorchidism: no evidence for involvement of genes underlying isolated hypogonadotropic hypogonadism. Molecular and cellular endocrinology 2011 Jul 341 (1-2): 35-8. Laitinen Eeva-Maria, Tommiska Johanna, Virtanen Helena E, Oehlandt Heidi, Koivu Rosanna, Vaaralahti Kirsi, Toppari Jorma, Raivio Tane |
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia. The Journal of clinical endocrinology and metabolism 2012 Feb . Raivio T, Avbelj M, McCabe MJ, Romero CJ, Dwyer AA, Tommiska J, Sykiotis GP, Gregory LC, Diaczok D, Tziaferi V, Elting MW, Padidela R, Plummer L, Martin C, Feng B, Zhang C, Zhou QY, Chen H, Mohammadi M, Quinton R, Sidis Y, Radovick S, Dattani MT, Pitteloud N |
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients. European journal of endocrinology / European Federation of Endocrine Societies 2013 Dec 169 (6): 805-9. Sarfati Julie, Fouveaut Corinne, Leroy Chrystel, Jeanpierre Marc, Hardelin Jean-Pierre, Dodé Catheri |
Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia. The Journal of clinical endocrinology and metabolism 2013 Mar 98 (3): E547-57. McCabe Mark J, Gaston-Massuet Carles, Gregory Louise C, Alatzoglou Kyriaki S, Tziaferi Vaitsa, Sbai Oualid, Rondard Philippe, Masumoto Koh-hei, Nagano Mamoru, Shigeyoshi Yasufumi, Pfeifer Marija, Hulse Tony, Buchanan Charles R, Pitteloud Nelly, Martinez-Barbera Juan-Pedro, Dattani Mehul |
Genetics of congenital hypogonadotropic hypogonadism in Denmark. European journal of medical genetics 2014 Jul 57 (7): 345-8. Tommiska Johanna, Känsäkoski Johanna, Christiansen Peter, Jørgensen Niels, Lawaetz Jacob Gerner, Juul Anders, Raivio Tane |
Huntington's disease biomarker progression profile identified by transcriptome sequencing in peripheral blood. European journal of human genetics : EJHG 2015 Oct 23 (10): 1349-56. Mastrokolias Anastasios, Ariyurek Yavuz, Goeman Jelle J, van Duijn Erik, Roos Raymund Ac, van der Mast Roos C, van Ommen GertJan B, den Dunnen Johan T, 't Hoen Peter Ac, van Roon-Mom Willeke |
Correlation between Pituitary Stalk Interruption Syndrome and Prokineticin Receptor 2 and Prokineticin 2 Mutations. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2016 Feb 38 (1): 37-41. Han Bai-Yu, Li Le-le, Wang Cheng-Zhi, Guo Qing-Hua, Lv Zhao-Hui, Mu Yi-Ming, Dou Jing-T |
Next-generation sequencing of patients with congenital anosmia. European journal of human genetics : EJHG 2017 12 25 (12): 1377-1387. Alkelai Anna, Olender Tsviya, Dode Catherine, Shushan Sagit, Tatarskyy Pavel, Furman-Haran Edna, Boyko Valery, Gross-Isseroff Ruth, Halvorsen Matthew, Greenbaum Lior, Milgrom Roni, Yamada Kazuya, Haneishi Ayumi, Blau Ilan, Lancet Dor |
A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers.
Frontiers in psychiatry 2018 9 290. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yu Younger W-Y, Yang Albert C, Tsai Shih-J |
New roles for prokineticin 2 in feeding behavior, insulin resistance and type 2 diabetes: Studies in mice and humans. Molecular metabolism 2019 11 29 182-196. Mortreux Marie, Foppen Ewout, Denis Raphaël G, Montaner Mireia, Kassis Nadim, Denom Jessica, Vincent Mylène, Fumeron Frédéric, Kujawski-Lafourcade Margaux, Andréelli Fabrizio, Balkau Beverley, Marre Michel, Roussel Ronan, Magnan Christophe, Gurden Hirac, Migrenne-Li Stéphan |
Differences in the Platelet mRNA Landscape Portend Racial Disparities in Platelet Function and Suggest Novel Therapeutic Targets. Clinical pharmacology and therapeutics 2021 7 110 (3): 702-713. Garofano Kaitlin, Park C Sehwan, Alarcon Cristina, Avitia Juan, Barbour April, Diemert David, Fraser Claire M, Friedman Paula N, Horvath Anelia, Rashid Kameron, Shaazuddin Mohammed, Sidahmed Alfateh, O'Brien Travis J, Perera Minoli A, Lee Norman |
Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism. Journal of pediatric endocrinology & metabolism : JPEM 2021 4 34 (6): 771-780. Turkyilmaz Ayberk, Cayir Atilla, Yarali Oguzhan, Kurnaz Erdal, Kartal Baykan Emine, Arslan Ates Esra, Demirbilek Husey |
Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review. Clinical endocrinology 2022 9 97 (6): 804-813. Patil Virendra A, Lila Anurag Ranjan, Shah Nalini, Arya Sneha, Sarathi Vijaya, Shah Ravikumar, Jadhav Swati S, Memon Saba Samad, Karlekar Manjiri, Bandgar Tush |
PROK2, HRNR, and FIG4 as potential genetic biomarkers of high bleeding propensity in East Asian patients with acute coronary syndrome using ticagrelor. Pharmacotherapy 2022 Oct . Xiang Qian, Wang Zhe, Mu Guangyan, Xie Qiufen, Liu Zhiyan, Zhou Shuang, Zhang Hanxu, Wang Zining, Hu Kun, Song Hongtao, Yuan Dongdong, Xia Quan, Huang Yan, Cui Yim |
Identification of PROK2 gene polymorphisms as predictors of methamphetamine use disorder risk and indicators of craving scale in the Chinese Han population. Frontiers in pharmacology 2023 7 14 1217382. Zhao Jiang, Tianxiao Zhang, Wei Han, Jing Xiao, Wenpei Zhang, Xiaochen Wang, Jianing Liu, Ying Yang, Congying Yang, Fanglin Guan, Tao Li, John P Ri |
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency. Journal of clinical research in pediatric endocrinology 2023 6 . Asl? Derya Kardelen, Adam Najafli, Firdevs Ba?, Birsen Karaman, Güven Toksoy, ?ükran Poyrazo?lu, ?ahin Avc?, Umut Altuno?lu, Zehra Yava? Abal?, Ay?e P?nar Öztürk, Esin Karak?l?ç Özturan, Seher Ba?aran, Feyza Darendeliler, Z Oya Uygun |
Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series. International journal of molecular sciences 2023 4 24 (8): . Rossella Cannarella, Carmelo Gusmano, Rosita A Condorelli, Andrea Bernini, Jurgen Kaftalli, Paolo Enrico Maltese, Stefano Paolacci, Astrit Dautaj, Giuseppe Marceddu, Matteo Bertelli, Sandro La Vignera, Aldo E Caloge |
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