Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 64 Records) |
Query Trace: PAX9[original query] |
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Novel Genetic Determinants of Dental Maturation in Children.
Journal of dental research 2022 11 102 (3): 349-356. Grgic O, Prijatelj V, Dudakovic A, Vucic S, Dhamo B, Trajanoska K, Monnereau C, Zrimsek M, Gautvik K M, Reppe S, Shimizu E, Haworth S, Timpson N J, Jaddoe V W V, Jarvelin M-R, Evans D, Uitterlinden A G, Ongkosuwito E M, van Wijnen A J, Medina-Gomez C, Rivadeneira F, Wolvius E |
Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation? Journal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie 2017 Feb . Bock Niko C, Lenz Sarah, Ruiz-Heiland Gisela, Ruf Sabi |
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
American journal of human genetics 2017 Dec 101 (6): 913-924. Shaffer John R, Li Jinxi, Lee Myoung Keun, Roosenboom Jasmien, Orlova Ekaterina, Adhikari Kaustabh, , Gallo Carla, Poletti Giovanni, Schuler-Faccini Lavinia, Bortolini Maria-Cátira, Canizales-Quinteros Samuel, Rothhammer Francisco, Bedoya Gabriel, González-José Rolando, Pfeffer Paige E, Wollenschlaeger Christopher A, Hecht Jacqueline T, Wehby George L, Moreno Lina M, Ding Anan, Jin Li, Yang Yajun, Carlson Jenna C, Leslie Elizabeth J, Feingold Eleanor, Marazita Mary L, Hinds David A, Cox Timothy C, Wang Sijia, Ruiz-Linares Andrés, Weinberg Seth |
Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series. European journal of oral sciences 2017 Nov . Haddaji Mastouri Marwa, De Coster Peter, Zaghabani Aicha, Jammali Frej, Raouahi Nabiha, Ben Salem Amina, Saad Ali, Coucke Paul, H'mida Ben Brahim Dor |
A Comprehensive cis-eQTL Analysis Revealed Target Genes in Breast Cancer Susceptibility Loci Identified in Genome-wide Association Studies. American journal of human genetics 2018 05 102 (5): 890-903. Guo Xingyi, Lin Weiqiang, Bao Jiandong, Cai Qiuyin, Pan Xiao, Bai Mengqiu, Yuan Yuan, Shi Jiajun, Sun Yaqiong, Han Mi-Ryung, Wang Jing, Liu Qi, Wen Wanqing, Li Bingshan, Long Jirong, Chen Jianghua, Zheng W |
WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population. Journal of genetics 2018 Dec 97 (5): 1169-1177. Grejtakova D, Gabrikova-Dojcakova D, Boronova I, Kyjovska L, Hubcejova J, Fecenkova M, Zigova M, Priganc M, Bernasovska |
The role of PAX9 promoter gene polymorphisms in causing hypodontia: a study in the Jordanian population. The application of clinical genetics 2018 11 145-149. Abu-Siniyeh Ahmed, Khabour Omar F, Owais Arwa |
WNT10B mutations associated with isolated dental anomalies. Clinical genetics 2018 1 93 (5): 992-999. Kantaputra P N, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns J |
Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2019 7 57 (1): 80-87. Shibano Masayasu, Watanabe Akira, Takano Nobuo, Mishima Hiroyuki, Kinoshita Akira, Yoshiura Koh-Ichiro, Shibahara Takahi |
Role of polymorphisms of MSX1 and PAX9 genes in palatal impaction of maxillary canines. Journal of orthodontics 2019 Mar 46 (1): 14-19. Devi M S Anjana, Padmanabhan Sride |
Genotyping analysis of the Pax9 Gene in patients with maxillary canine impaction. F1000Research 2019 5 8 254. Vitria Evy Eida, Tofani Iwan, Kusdhany Lindawati, Bachtiar Endang Winia |
Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia. BioMed research international 2019 2019 2183720. Mártha Krisztina, Kerekes Máthé Bernadette, Moldovan Valeriu George, B?nescu Claud |
Six2 regulates Pax9 expression, palatogenesis and craniofacial bone formation. Developmental biology 2019 11 458 (2): 246-256. Sweat Yan Yan, Sweat Mason, Mansaray Maurisa, Cao Huojun, Eliason Steven, Adeyemo Waisu L, Gowans Lord J J, Eshete Mekonen A, Anand Deepti, Chalkley Camille, Saadi Irfan, Lachke Salil A, Butali Azeez, Amendt Brad |
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.
PLoS genetics 2019 10 15 (10): e1008357. Huang Lulin, Jia Zhonglin, Shi Yi, Du Qin, Shi Jiayu, Wang Ziyan, Mou Yandong, Wang Qingwei, Zhang Bihe, Wang Qing, Ma Shi, Lin He, Duan Shijun, Yin Bin, Lin Yansong, Wang Yiru, Jiang Dan, Hao Fang, Zhang Lin, Wang Haixin, Jiang Suyuan, Xu Huijuan, Yang Chengwei, Li Chenghao, Li Jingtao, Shi Bing, Yang Zhengl |
Common variants of EDA are associated with non-syndromic hypodontia. Orthodontics & craniofacial research 2020 Aug . Al-Ani Azza H, Antoun Joseph S, Thomson William M, Topless Ruth, Merriman Tony R, Farella Mau |
Mutation at Paired box gene 9 is associated with non-syndromic cleft lip only from Western Han Chinese population. Archives of oral biology 2020 Jul 117 104829. Yang Cheng-Wei, Shi Jia-Yu, Yin Bin, Shi Bing, Jia Zhong-L |
Genetic variants in tooth agenesis-related genes might be also involved in tooth size variations. Clinical oral investigations 2020 Jul . Cunha Arthur S, Dos Santos Luiza Vertuan, Marañón-Vásquez Guido Artemio, Kirschneck Christian, Gerber Jennifer Tsi, Stuani Maria Bernadete, Matsumoto Mírian Aiko Nakane, Vieira Alexandre Rezende, Scariot Rafaela, Küchler Erika Calva |
Family-based association study of genetic analysis of paired box gene 9 polymorphisms in the peg-shaped teeth in the Jordanian Arab population. Archives of oral biology 2020 11 121 104966. Alkhatib Rami, Obeidat Bayan, Al-Eitan Laith, Abdo Nour, Obeidat Fadi, Aman Hat |
Screening PAX9, MSX1 and WNT10A Mutations in 4 Iranian Families with Non-Syndromic Tooth Agenesis. Avicenna journal of medical biotechnology 2020 10 12 (4): 236-240. Safari Shiva, Ebadifar Asghar, Najmabadi Hossien, Kamali Koorosh, Abedini Seyedeh Sedigh |
Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation. Oral diseases 2021 7 29 (1): 300-307. Ross Jamila N, Ruigrok Lisanne C, Fennis Willem M M, Cune Marco S, Rosenberg Antoine J W P, van Nunen Annick B, Créton Marijn A, Ploos van Amstel Hans-Kristian, van den Boogaard Marie-José J |
BAX -248 G>A and BCL2 -938 C>A Variant Lowers the Survival in Patients with Nasopharyngeal Carcinoma and Could be Associated with Tissue-Specific Malignancies: A Multi-Method Approach. Asian Pacific journal of cancer prevention : APJCP 2021 Apr 22 (4): 1171-1181. Chatterjee Koustav, De Saikat, Deb Roy Sankar, Sahu Sushil Kumar, Chakraborty Arindom, Ghatak Sandeep, Das Nilanjana, Mal Sudipa, Roy Chattopadhyay Nabanita, Das Piyanki, Reddy R Rajendra, Mukherjee Syamantak, Das Ashok Kumar, Puii Zoreng, Zomawia Eric, Singh Yengkhom Indibor, Tsering Sam, Riba Komri, Rajasubramaniam Shanmugam, Suryawanshi Amol Ratnakar, Choudhuri Tathaga |
Functional Screenings Identify Regulatory Variants Associated with Breast Cancer Susceptibility. Current issues in molecular biology 2021 12 43 (3): 1756-1777. Ren Naixia, Li Yingying, Xiong Yulong, Li Panfeng, Ren Yutian, Huang Qil |
Analyses of oligodontia phenotypes and genetic etiologies. International journal of oral science 2021 10 13 (1): 32. Zhou Mengqi, Zhang Hong, Camhi Heather, Seymen Figen, Koruyucu Mine, Kasimoglu Yelda, Kim Jung-Wook, Kim-Berman Hera, Yuson Ninna M R, Benke Paul J, Wu Yiqun, Wang Feng, Zhu Yaqin, Simmer James P, Hu Jan C |
Patterns of molar agenesis associated with p.P20L and p.R77Q variants in PAX9. European journal of oral sciences 2022 2 130 (2): e12855. Intarak Narin, Theerapanon Thanakorn, Porntaveetus Thantrira, Shotelersuk Voras |
Genetics of three-dimensional tooth inclination and angulation in orthodontic patients with Class I Occlusion: A cross-sectional study. International orthodontics 2022 12 21 (1): 100713. ElNaghy Rahma, Daabous Andrew Thomas, Hasanin Majd, Tanha Nazanin, Ancona Nicholas, Al-Qawasmi Riy |
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes. Human genetics 2023 9 . Sarah W Curtis, Jenna C Carlson, Terri H Beaty, Jeffrey C Murray, Seth M Weinberg, Mary L Marazita, Justin L Cotney, David J Cutler, Michael P Epstein, Elizabeth J Lesl |
Genetic Factors of Teeth Impaction: Polymorphic and Haplotype Variants of PAX9, MSX1, AXIN2, and IRF6 Genes. International journal of molecular sciences 2023 9 24 (18): . Grzegorz Trybek, Aleksandra Jaro?, Ewa Gabrysz-Trybek, Monika Rutkowska, Aleksandra Markowska, Krzysztof Chmielowiec, Jolanta Chmielowiec, Anna Grzywa |
Tooth agenesis patterns and variants in PAX9: A systematic review. The Japanese dental science review 2023 5 59 129-137. Narin Intarak, Karn Tongchairati, Kittipat Termteerapornpimol, Soranun Chantarangsu, Thantrira Porntaveet |
The phenotype and genotype of PAX9 mutations causing tooth agenesis. Clinical oral investigations 2023 5 . Cailing Jiang, Kang Yu, Yihan Shen, Feng Wang, Qinggang Dai, Yiqun |
Rare genetic variants in SEC24D modify orofacial cleft phenotypes. medRxiv : the preprint server for health sciences 2023 4 . Curtis Sarah W, Carlson Jenna C, Beaty Terri H, Murray Jeffrey C, Weinberg Seth M, Marazita Mary L, Cotney Justin L, Cutler David J, Epstein Michael P, Leslie Elizabeth |
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- Page last updated:Apr 29, 2024
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