Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: SPRY2[original query] |
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Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS genetics 2005 Dec 1 (6): e64. Vieira Alexandre R, Avila Joseph R, Daack-Hirsch Sandra, Dragan Ecaterina, Félix Têmis M, Rahimov Fedik, Harrington Jill, Schultz Rebecca R, Watanabe Yoriko, Johnson Marla, Fang Jennifer, O'Brien Sarah E, Orioli Iêda M, Castilla Eduardo E, Fitzpatrick David R, Jiang Rulang, Marazita Mary L, Murray Jeffrey |
Search for pathogenetic variants of the SPRY2 gene in intestinal innervation defects. Internal medicine journal 2009 May 39 (5): 335-7. Borghini S, Duca M Di, Pini Prato A, Lerone M, Martucciello G, Jasonni V, Ravazzolo R, Ceccherini |
Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population. Diabetologia 2011 Dec 54 (12): 3071-7. Imamura M, Iwata M, Maegawa H, Watada H, Hirose H, Tanaka Y, Tobe K, Kaku K, Kashiwagi A, Kawamori R, Nakamura Y, Maeda |
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
Nature genetics 2011 Jun . Kilpeläinen TO, Zillikens MC, Stan?ákova A, Finucane FM, Ried JS, Langenberg C, Zhang W, Beckmann JS, Luan J, Vandenput L, Styrkarsdottir U, Zhou Y, Smith AV, Zhao JH, Amin N, Vedantam S, Shin SY, Haritunians T, Fu M, Feitosa MF, Kumari M, Halldorsson BV, Tikkanen E, Mangino M, Hayward C, Song C, Arnold AM, Aulchenko YS, Oostra BA, Campbell H, Cupples LA, Davis KE, Döring A, Eiriksdottir G, Estrada K, Fernández-Real JM, Garcia M, Gieger C, Glazer NL, Guiducci C, Hofman A, Humphries SE, Isomaa B, Jacobs LC, Jula A, Karasik D, Karlsson MK, Khaw KT, Kim LJ, Kivimäki M, Klopp N, Kühnel B, Kuusisto J, Liu Y, Ljunggren O, Lorentzon M, Luben RN, McKnight B, Mellström D, Mitchell BD, Mooser V, Moreno JM, Männistö S, O'Connell JR, Pascoe L, Peltonen L, Peral B, Perola M, Psaty BM, Salomaa V, Savage DB, Semple RK, Skaric-Juric T, Sigurdsson G, Song KS, Spector TD, Syvänen AC, Talmud PJ, Thorleifsson G, Thorsteinsdottir U, Uitterlinden AG, van Duijn CM, Vidal-Puig A, Wild SH, Wright AF, Clegg DJ, Schadt E, Wilson JF, Rudan I, Ripatti S, Borecki IB, Shuldiner AR, Ingelsson E, Jansson JO, Kaplan RC, Gudnason V, Harris TB, Groop L, Kiel DP, Rivadeneira F, Walker M, Barroso I, Vollenweider P, Waeber G, Chambers JC, Kooner JS, Soranzo N, Hirschhorn JN, Stefansson K, Wichmann HE, Ohlsson C, O'Rahilly S, Wareham NJ, Speliotes EK, Fox CS, Laakso M, Loos RJ |
NUDT3 rs206936 is associated with body mass index in obese Japanese women. Endocrine journal 2013 60 (8): 991-1000. Kitamoto Aya, Kitamoto Takuya, Mizusawa Seiho, Teranishi Hajime, So Rina, Matsuo Tomoaki, Nakata Yoshio, Hyogo Hideyuki, Ochi Hidenori, Nakamura Takahiro, Kamohara Seika, Miyatake Nobuyuki, Kotani Kazuaki, Komatsu Ryoya, Itoh Naoto, Mineo Ikuo, Wada Jun, Yoneda Masato, Nakajima Atsushi, Funahashi Tohru, Miyazaki Shigeru, Tokunaga Katsuto, Masuzaki Hiroaki, Ueno Takato, Chayama Kazuaki, Hamaguchi Kazuyuki, Yamada Kentaro, Hanafusa Toshiaki, Oikawa Shinichi, Sakata Toshiie, Tanaka Kiyoji, Matsuzawa Yuji, Nakao Kazuwa, Sekine Akihiro, Hotta Kiku |
Identification of genetic risk factors for maxillary lateral incisor agenesis. Journal of dental research 2014 May 93 (5): 452-8. Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso |
Association between NOGGIN and SPRY2 polymorphisms and nonsyndromic cleft lip with or without cleft palate. American journal of medical genetics. Part A 2015 Jan 167A (1): 137-41. Song Tao, Shi Jinna, Guo Qiang, Lv Kewen, Jiao Xiaohui, Hu Tenglong, Sun Xiangyu, Fu Songb |
Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans. American journal of medical genetics. Part A 2015 May 167A (5): 1054-60. Jia Zhonglin, Leslie Elizabeth J, Cooper Margaret E, Butali Azeez, Standley Jennifer, Rigdon Jennifer, Suzuki Satoshi, Gongorjav Ayana, Shonkhuuz T Enkhtur, Natsume Nagato, Shi Bing, Marazita Mary L, Murray Jeffrey |
Single nucleotide polymorphisms in microRNA genes are associated with cervical cancer susceptibility in a population from Xinjiang Uygur. Oncotarget 2016 Sep . Yang Jie, Zhang Zegao, Guo Wen, Ma Yuhua, Muhammed Emin Raila, Abudubari Karima, Hayrat Glmira, Wali Hasiyet, Qi Xiaoli, Liu Chunhua, Ma Miaomiao, Nurbek Pul |
Predictors of Hand-Foot Syndrome and Pyridoxine for Prevention of Capecitabine-Induced Hand-Foot Syndrome: A Randomized Clinical Trial. JAMA oncology 2017 Jul . Yap Yoon-Sim, Kwok Li-Lian, Syn Nicholas, Chay Wen Yee, Chia John Whay Kuang, Tham Chee Kian, Wong Nan Soon, Lo Soo Kien, Dent Rebecca Alexandra, Tan Sili, Mok Zuan Yu, Koh King Xin, Toh Han Chong, Koo Wen Hsin, Loh Marie, Ng Raymond Chee Hui, Choo Su Pin, Soong Richie Chuan Te |
A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts. Journal of dental research 2017 Oct 96 (11): 1322-1329. Moreno Uribe L M, Fomina T, Munger R G, Romitti P A, Jenkins M M, Gjessing H K, Gjerdevik M, Christensen K, Wilcox A J, Murray J C, Lie R T, Wehby G |
Genome-Wide Association Study Links Receptor Tyrosine Kinase Inhibitor Sprouty 2 to Thrombocytopenia after Coronary Artery Bypass Surgery.
Thrombosis and haemostasis 2018 Aug . Karhausen Jörn A, Qi Wenjing, Smeltz Alan M, Li Yi-Ju, Shah Svati H, Kraus William E, Mathew Joseph P, Podgoreanu Mihai V, Kertai Miklos D, |
Gene-Gene Interactions among SPRYs for Nonsyndromic Cleft Lip/Palate. Journal of dental research 2018 10 98 (2): 180-185. Zhou R, Wang M, Li W, Wang S, Zhou Z, Li J, Wu T, Zhu H, Beaty T |
[Exploring the association between SPRY gene family and non-syndromic oral clefts among Chinese populations using data of a next-generation sequencing study]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2019 Jun 51 (3): 564-570. Zhou R, Zheng H C, Li W Y, Wang M Y, Wang S Y, Li N, Li J, Zhou Z B, Wu T, Zhu H |
Haplotype and Haplotype-Environment Interaction Analysis Revealed Roles of SPRY2 for NSCL/P among Chinese Populations. International journal of environmental research and public health 2019 Feb 16 (4): . Zhou Ren, Wang Mengying, Li Wenyong, Wang Siyue, Zheng Hongchen, Zhou Zhibo, Hu Yonghua, Li Jing, Wu Tao, Zhu Hongping, Beaty Terri |
Population history and genetic adaptation of the Fulani nomads: inferences from genome-wide data and the lactase persistence trait.
BMC genomics 2019 Dec 20 (1): 915. Vicente Mário, Priehodová Edita, Diallo Issa, Podgorná Eliška, Poloni Estella S, ?erný Viktor, Schlebusch Carina |
Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism. Journal of medical genetics 2020 5 58 (1): 66-72. Men Meichao, Wang Xinying, Wu Jiayu, Zeng Wang, Jiang Fang, Zheng Ruizhi, Li Jia- |
Allele-specific transcription factor binding in a cellular model of orofacial clefting. Scientific reports 2022 2 12 (1): 1807. Ruff Katharina L M, Hollstein Ronja, Fazaal Julia, Thieme Frederic, Gehlen Jan, Mangold Elisabeth, Knapp Michael, Welzenbach Julia, Ludwig Kerstin |
The Prognostic and Functional Impact of Sprouty 2 Expression in Non-small Cell Lung Cancer. American journal of clinical oncology 2023 9 . Yusuf Acikgoz, Fatma Unal Yildirim, Selin Akturk Esen, Gokhan Ucar, Yakup Ergun, Oznur Bal, Mutlu Dogan, Dogan Un |
Dual role of sprouty2 as an inhibitor of RAS/ERK-driven proliferation and a promoter of cancer invasion in KRAS wild-type colorectal cancer. Molecular carcinogenesis 2023 4 . Lee Chung-Ta, Chu Chien-An, Wang Yu-Ming, Wang Yi-Wen, Chen Yi-Lin, Ho Chung-Liang, Yeh Yu-Min, Lin Peng-Chan, Lin Bo-Wen, Chen Po-Chuan, Chen Shang-Hung, Chan Ren-Hao, Chang Chen, Chow Nan-H |
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