Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 81 Records) |
Query Trace: RUNX2[original query] |
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Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis.
Nature communications 2023 5 14 (1): 2644. Sethi Anurag, Ruby J Graham, Veras Matthew A, Telis Natalie, Melamud Euge |
Distinct association of RUNX family expression with genetic alterations and clinical outcome in acute myeloid leukemia. Cancer biomarkers : section A of Disease markers 2020 8 29 (3): 387-397. Zhao Yangli, Zhang Tingjuan, Zhao Yangjing, Zhou Jingdo |
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis. Bone 2020 Apr 115395. Cuellar Araceli, Bala Krithi, Di Pietro Lorena, Barba Marta, Yagnik Garima, Liu Jia Lie, Stevens Christina, Hur David J, Ingersoll Roxann G, Justice Cristina M, Drissi Hicham, Kim Jinoh, Lattanzi Wanda, Boyadjiev Simeon |
Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes. Heliyon 2020 12 6 (11): e05632. Hussein Deema, Dallol Ashraf, Quintas Rita, Schulten Hans-Juergen, Alomari Mona, Baeesa Saleh, Bangash Mohammed, Alghamdi Fahad, Khan Ishaq, ElAssouli M-Zaki Mustafa, Saka Mohamad, Carracedo Angel, Chaudhary Adeel, Abuzenadah Ad |
Investigation of Genetic Polymorphisms in BMP2, BMP4, SMAD6, and RUNX2 and Persistent Apical Periodontitis. Journal of endodontics 2020 Nov . Küchler Erika Calvano, Hannegraf Natascha Douat, Lara Rafaela Mariana, Reis Caio Luiz Bitencourt, Oliveira Daniela Silva Barroso de, Mazzi-Chaves Jardel Francisco, Ribeiro Andrades Kesly Mary, Lima Lorena Ferreira de, Salles Alessandro Guimarães, Antunes Livia Azeredo Alves, Sousa-Neto Manoel Damião, Antunes Leonardo Santos, Baratto-Filho Flar |
RUNX2 and IL-15RA Polymorphisms associated with OPLL in the Han and Mongolian population. JPMA. The Journal of the Pakistan Medical Association 2020 Sep 70 [Special Issue] (9): 98-104. Li Pengfei, Liu Zongzheng, Liu Jianfeng, Xing Wei, Fu Haiping, Zhu Shuf |
Potential interactions among single nucleotide polymorphisms in bone- and cartilage-related genes in skeletal malocclusions. Orthodontics & craniofacial research 2020 Oct . Küchler Erika Calvano, Reis Caio Luiz Bitencourt, Carelli Julia, Scariot Rafaela, Nelson-Filho Paulo, Coletta Ricardo D, Paza Aleysson Olimpio, Matsumoto Mírian Aiko Nakane, Proff Peter, Kirschneck Christi |
USF3 modulates osteoporosis risk by targeting WNT16, RANKL, RUNX2, and two GWAS lead SNPs rs2908007 and rs4531631. Human mutation 2020 10 42 (1): 37-49. Ye Weiyuan, Wang Ya, Hou Sasa, Mei Bing, Liu Xinhong, Huang Han, Zhou Qian, Niu Yajing, Chen Yuanyuan, Zhang Manling, Huang Qingya |
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene.
Annals of the rheumatic diseases 2020 10 . Boer Cindy Germaine, Yau Michelle S, Rice Sarah J, Coutinho de Almeida Rodrigo, Cheung Kathleen, Styrkarsdottir Unnur, Southam Lorraine, Broer Linda, Wilkinson Jeremy Mark, Uitterlinden André G, Zeggini Eleftheria, Felson David, Loughlin John, Young Mariel, Capellini Terence Dante, Meulenbelt Ingrid, van Meurs Joyce |
Exploring the Association Between Genetic Polymorphisms in Genes Involved in Craniofacial Development and Isolated Tooth Agenesis. Frontiers in physiology 2021 9 12 723105. Küchler Erika Calvano, Reis Caio Luiz Bitencourt, Silva-Sousa Alice Corrêa, Marañón-Vásquez Guido Artemio, Matsumoto Mirian Aiko Nakane, Sebastiani Aline, Scariot Rafaela, Paddenberg Eva, Proff Peter, Kirschneck Christi |
Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia. Iranian biomedical journal 2021 7 25 (4): 297-302. Jamali Ebrahim, Khalesi Raziyeh, Bitarafan Fatemeh, Almadani Navid, Garshasbi Maso |
The importance of NF?B1 rs4648068 and RUNX2 rs7771980 polymorphisms in bone metabolism of postmenopausal Polish women. Ginekologia polska 2021 Apr . Bogacz Anna, Gorska Aleksandra, Kaminski Adam, Wolek Marlena, Wolski Hubert, Seremak-Mrozikiewicz Agnieszka, Goracy Jaroslaw, Czerny Bogusl |
Predicted regulatory SNPs reveal potential drug targets and novel companion diagnostics in psoriasis. Journal of translational autoimmunity 2021 4 100096. Ruiz Ramírez Andrea Virginia, Flores-Saiffe Farías Adolfo, Chávez Álvarez Rocío Del Carmen, Prado Montes de Oca Ernes |
Odontogenesis-related candidate genes involved in variations of permanent teeth size. Clinical oral investigations 2021 3 25 (7): 4481-4494. Gerber Jennifer Tsi, Dos Santos Katheleen Miranda, Brum Bruna Karas, Petinati Maria Fernanda Pivetta, Meger Michelle Nascimento, da Costa Delson João, Elsalanty Mohammed, Küchler Erika Calvano, Scariot Rafae |
The Polymorphism at PLCB4 Promoter (rs6086746) Changes the Binding Affinity of RUNX2 and Affects Osteoporosis Susceptibility: An Analysis of Bioinformatics-Based Case-Control Study and Functional Validation. Frontiers in endocrinology 2021 12 12 730686. Tsai Dung-Jang, Fang Wen-Hui, Wu Li-Wei, Tai Ming-Cheng, Kao Chung-Cheng, Huang Shih-Ming, Chen Wei-Teing, Hsiao Po-Jen, Chiu Chih-Chien, Su Wen, Wu Chia-Chun, Su Sui-Lu |
The Wnt/?-catenin signaling pathway has a healing ability for periapical periodontitis. Scientific reports 2021 10 11 (1): 19673. Naruse Haruna, Itoh Shousaku, Itoh Yuki, Kagioka Takumi, Abe Makoto, Hayashi Mika |
Understanding the role of corneal biomechanics-associated genetic variants by bioinformatic analyses. International ophthalmology 2021 10 42 (3): 981-988. Sun Xiao, Gao Xiang, Mu Bo-Kun, Wang Y |
Association of type 2 diabetes mellitus and periodontal disease susceptibility with genome-wide association-identified risk variants in a Southeastern Brazilian population. Clinical oral investigations 2021 Jan . Cirelli Thamiris, Nepomuceno Rafael, Goveia Jéssica Marina, Orrico Silvana R P, Cirelli Joni A, Theodoro Letícia Helena, Barros Silvana P, Scarel-Caminaga Raquel |
Genetics of progressive supranuclear palsy in a Chinese population. Neurobiology of disease 2022 Jul 172 105819. Xiao Xuewen, Yang Qijie, Wen Yafei, Jiao Bin, Liao Xinxin, Zhou Yafang, Weng Ling, Liu Hui, Xu Tianyan, Zhu Yuan, Guo Lina, Zhou Lu, Wang Xin, Liu Xixi, Bi Xiangyun, Liu Yingzi, Zhang Sizhe, Zhang Weiwei, Li Jinchen, Tang Beisha, Shen |
Prognostic value and immune characteristics of RUNX gene family in human cancers: a pan-cancer analysis. Aging 2022 5 14 (9): 4014-4035. Zhao Han, Chen Yun, Shen Peijun, Gong L |
Evaluation of cfDNA as an early detection assay for dense tissue breast cancer. Scientific reports 2022 May 12 (1): 8458. Barbirou Mouadh, Miller Amanda A, Gafni Erik, Mezlini Amel, Zidi Asma, Boley Nathan, Tonellato Peter |
Single Nucleotide Polymorphisms in Runt-related Transcription Factor 2 and Bone Morphogenetic Protein 2 Impact on Their Maxillary and Mandibular Gene Expression in Different Craniofacial Patterns - A Comparative Study. Annals of maxillofacial surgery 2022 3 11 (2): 222-228. Olsson Bernardo, da Silva Mateus José, Lago Camila, Calixto Robson Diego, Ramazzotto Lucas Alexandre, Barbosa Rebellato Nelson Luis, Kirschneck Christian, Garcia Paula-Silva Francisco Wanderley, Küchler Erika Calvano, Scariot Rafae |
Association between SEMA3A signaling pathway genes and BMD/OP risk: An epidemiological and experimental study. Frontiers in endocrinology 2022 11 13 1014431. Zhou Hao-Long, Wei Mu-Hong, Di Dong-Sheng, Zhang Ru-Yi, Zhang Jian-Li, Yuan Ting-Ting, Liu Qian, Zhou Ting-Ting, Huang Qin, Wang |
WNT10A and RUNX2 mutations associated with non-syndromic tooth agenesis. European journal of oral sciences 2022 10 130 (6): e12896. Živkovi? Marija, Stefanovi? Neda, Gliši? Branislav, Brajovi? Gavrilo, Mili?i? Biljana, Kosti? Marija, Popovi? Bran |
Analysis of Zinc and Stromal Immunity in Disuse Osteoporosis: Mendelian Randomization and Transcriptomic Analysis. Orthopaedic surgery 2023 9 . Fei Lyu, Li Wang, Yiming Jia, Yuanlin Wang, Haolan Qi, Zhengxu Dai, Xuyang Zhou, Haoran Zhu, Bing Li, Yujing Xu, Jun L |
Impact of genetic variations in the WNT family members and RUNX2 on dental and skeletal maturation: a cross-sectional study. Head & face medicine 2023 7 19 (1): 26. Caio Luiz Bitencourt Reis, Mirian Aiko Nakane Matsumoto, Flares Baratto-Filho, Rafaela Scariot, Maria Bernadete Sasso Stuani, Fábio Lourenço Romano, Ricardo Della Coletta, Daniela Silva Barroso de Oliveira, Peter Proff, Christian Kirschneck, Erika Calvano Küchl |
Associations between Host Genetic Variants and Subgingival Microbiota in Patients with the Metabolic Syndrome. International journal of molecular sciences 2023 12 24 (23): . Luigi Nibali, Abish S Stephen, Robert P Allaker, Antonino Di Pino, Valentina Terranova, Marcella Pisano, Salvatore Di Marca, Viviana Ferrara, Roberto Scicali, Francesco Purrello, Nikolaos Donos, Matteo Regolo, Lorenzo Malati |
Polymorphisms in the Runx2 and osteocalcin genes affect BMD in postmenopausal women: a systematic review and meta-analysis. Endocrine 2023 12 . Somali Sanyal, Swati Rajput, Sreyanko Sadhukhan, Singh Rajender, Ambrish Mithal, Naibedya Chattopadhy |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
Nature communications 2023 1 14 (1): 157. Rämö Joel T, Kiiskinen Tuomo, Seist Richard, Krebs Kristi, Kanai Masahiro, Karjalainen Juha, Kurki Mitja, Hämäläinen Eija, Häppölä Paavo, Havulinna Aki S, Hautakangas Heidi, , Mägi Reedik, Palta Priit, Esko Tõnu, Metspalu Andres, Pirinen Matti, Karczewski Konrad J, Ripatti Samuli, Milani Lili, Stankovic Konstantina M, Mäkitie Antti, Daly Mark J, Palotie Aar |
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- Page last updated:Apr 22, 2024
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