Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 112 Records) |
| Query Trace: MSX1[original query] |
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| 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 |
| TGF?3, MSX1, and MMP3 as Candidates for NSCL±P in an Indian Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2018 Jan 1055665618775727. Kumari Priyanka, Singh Subodh Kumar, Raman Raji |
| Gene-gene interaction for nonsyndromic cleft lip with or without cleft palate in Chilean case-parent trios. Archives of oral biology 2018 4 91 91-95. Suazo José, Santos José Luis, Colombo Alicia, Pardo Ro |
| MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts: a meta-analysis. European journal of oral sciences 2018 Apr . Gu Min, Zhang Yan, Liu Hualian, Liu Jue, Zhu Danxia, Yang |
| Application of high-resolution array platform for genome-wide copy number variation analysis in patients with nonsyndromic cleft lip and palate. Journal of clinical laboratory analysis 2018 3 32 (6): e22428. da Silva Heglayne Pereira Vital, Oliveira Gustavo Henrique de Medeiros, Ururahy Marcela Abbott Galvão, Bezerra João Felipe, de Souza Karla Simone Costa, Bortolin Raul Hernandes, Luchessi André Ducati, Silbiger Vivian Nogueira, Lima Valéria Morgiana Gualberto Duarte Moreira, Leite Gisele Correia Pacheco, Brito Maria Edinilma Felinto, Ribeiro Erlane Marques, Gil-da-Silva-Lopes Vera Lúcia, de Rezende Adriana Augus |
| Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. Frontiers in genetics 2018 11 9 502. Indencleef Karlijne, Roosenboom Jasmien, Hoskens Hanne, White Julie D, Shriver Mark D, Richmond Stephen, Peeters Hilde, Feingold Eleanor, Marazita Mary L, Shaffer John R, Weinberg Seth M, Hens Greet, Claes Pet |
| 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 |
| Gene-gene interaction between MSX1 and TP63 in Asian case-parent trios with nonsyndromic cleft lip with or without cleft palate. Birth defects research 2018 Jan . Liu Dongjing, Schwender Holger, Wang Mengying, Wang Hong, Wang Ping, Zhu Hongping, Zhou Zhibo, Li Jing, Wu Tao, Beaty Terri |
| 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 |
| MSX1 gene polymorphisms and non-syndromic cleft lip with or without palate (NSCL/P): A meta-analysis. Oral diseases 2019 May . Tasanarong Parinda, Pabalan Noel, Tharabenjasin Phuntila, Jarjanazi Ham |
| 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 |
| Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank. Scientific reports 2019 Nov 9 (1): 16515. Córdova-Palomera Aldo, Priest James |
| Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis. Archives of oral biology 2019 Sep 109 104556. Lancia Melissa, Machado Renato Assis, Dionísio Thiago José, Garib Daniela Gamba, Santos Carlos Ferreira Dos, Coletta Ricardo D, Neves Lucimara Teixeira d |
| 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 |
| 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 |
| Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate. Human genetics 2020 4 139 (10): 1261-1272. Morris Vershanna E, Hashmi S Shahrukh, Zhu Lisha, Maili Lorena, Urbina Christian, Blackwell Steven, Greives Matthew R, Buchanan Edward P, Mulliken John B, Blanton Susan H, Zheng W Jim, Hecht Jacqueline T, Letra Ariad |
Congenital heart disease risk loci identified by genome-wide association study in European patients.
The Journal of clinical investigation 2020 Nov . Lahm Harald, Jia Meiwen, Dreßen Martina, Wirth Felix, Puluca Nazan, Gilsbach Ralf, Keavney Bernard D, Cleuziou Julie, Beck Nicole, Bondareva Olga, Dzilic Elda, Burri Melchior, König Karl C, Ziegelmüller Johannes A, Abou-Ajram Claudia, Neb Irina, Zhang Zhong, Doppler Stefanie A, Mastantuono Elisa, Lichtner Peter, Eckstein Gertrud, Hörer Jürgen, Ewert Peter, Priest James R, Hein Lutz, Lange Rüdiger, Meitinger Thomas, Cordell Heather J, Müller-Myhsok Bertram, Krane Mark |
| 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 |
| Association of Polymorphic and Haplotype Variants of the MSX1 Gene and the Impacted Teeth Phenomenon. Genes 2021 4 12 (4): . Trybek Grzegorz, Jaro? Aleksandra, Grzywacz An |
| Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort. Journal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie 2021 3 83 (Suppl 1): 65-74. Keskin Gül, Karaer Kadri, Uçar Gündo?ar Zübey |
| Unraveling the genomic basis of congenital heart disease. The Journal of clinical investigation 2021 Jan 131 (2): . Darbar Dawo |
| A single-nucleotide-polymorphism in the 5'-flanking region of MSX1 gene as a predictive marker candidate for platinum-based therapy of esophageal carcinoma. Therapeutic advances in medical oncology 2022 3 14 17588359221080580. Mori Takahiro, Ueno Kazuko, Tokunaga Katsushi, Kawai Yosuke, Matsuda Koichi, Nishida Nao, Komine Keigo, Saito Sakae, Nagasaki Masao, |
| 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 |
| Identification of tumour antigens and immune subtypes in the development of an anti-cancer vaccine for endometrial carcinoma. Scandinavian journal of immunology 2022 12 97 (3): e13250. Feng Jianyang, He Ho |
| Family and case-control genetic study of MSX1 polymorphisms in peg-shaped teeth Jordanian population. BMC oral health 2022 Jan 22 (1): 16. Alkhatib Rami, Hawamdeh Razan, Al-Eitan Laith, Abdo Nour, Obeidat Fadi, Al-Bataineh Mohamed, Aman Hat |
| 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 |
| Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2023 7 10556656231185218. Anny Memon, Fariha Fatima Khidiri, Yar Muhammad Waryah, Roohi Nigar, Munir Ahmad Bhinder, Ahmed Muhammad Shaikh, Hina Shaikh, Ali Muhammad Wary |
| MSX1 Gene Polymorphisms in Patients with non-Syndromic Cleft lip and Palate: A Tertiary Care Centre Based Case-Control Study from Central Kerala. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2023 11 10556656231214131. Arun Jyothish, Alex George, Puthucode V Narayanan, Rajanikant Golgodu Krishnamurt |
| Genetic and Morphological Variation in Hypodontia of Maxillary Lateral Incisors. Genes 2023 1 14 (1): . Kerekes-Máthé Bernadette, Mártha Krisztina, B?nescu Claudia, O'Donnell Matthew Brook, Brook Alan |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
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