Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: SNAI2[original query] |
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Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects. American journal of medical genetics. Part A 2014 Feb 164A (2): 397-406. Osoegawa Kazutoyo, Iovannisci David M, Lin Bin, Parodi Christina, Schultz Kathleen, Shaw Gary M, Lammer Edward |
[Endometrial cancer in young women--clinical and molecular aspects]. Ginekologia polska 2014 12 85 (10): 754-9. Lapi?ska-Szumczyk Sylwia, Supernat Anna, ?aczek Anna J, Majewska Hanna, Gulczy?ski Jacek, Sawicki Sambor, Biernat Wojciech, Wydra Dariu |
[Mutation analysis of seven patients with Waardenburg syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Jun 33 (3): 312-5. Hao Ziqi, Zhou Yongan, Li Pengli, Zhang Quanbin, Li Jiao, Wang Pengfei, Li Xiangshao, Feng Yo |
Clinical and genetic investigation of families with type II Waardenburg syndrome. Molecular medicine reports 2016 Jan . Chen Yong, Yang Fuwei, Zheng Hexin, Zhou Jianda, Zhu Ganghua, Hu Peng, Wu Weiji |
A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients. International journal of molecular and cellular medicine 2018 9 7 (1): 17-23. Jalilian Nazanin, Tabatabaiefar Mohammad Amin, Yazdanpanah Mahboubeh, Darabi Elham, Bahrami Tayyeb, Zekri Ali, Noori-Daloii Mohammad Re |
Analysis of the expression of cancer-associated fibroblast- and EMT-related proteins in submucosal invasive colorectal cancer. Journal of Cancer 2018 8 9 (15): 2702-2712. Sugai Tamotsu, Uesugi Noriyuki, Kitada Yuriko, Yamada Noriyuki, Osakabe Mitsumasa, Eizuka Makoto, Sugimoto Ryo, Fujita Yasuko, Kawasaki Keisuke, Yamamoto Eiichiro, Yamano Hiroo, Suzuki Hiromu, Matsumoto Takayu |
MEIS1 and MEIS2 Expression and Prostate Cancer Progression: A Role For HOXB13 Binding Partners in Metastatic Disease. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 5 24 (15): 3668-3680. Bhanvadia Raj R, VanOpstall Calvin, Brechka Hannah, Barashi Nimrod S, Gillard Marc, McAuley Erin M, Vasquez Juan Manuel, Paner Gladell, Chan Wen-Ching, Andrade Jorge, De Marzo Angelo M, Han Misop, Szmulewitz Russell Z, Vander Griend Donald |
Clinical significance of YAP1 activation in head and neck squamous cell carcinoma. Oncotarget 2017 Dec 8 (67): 111130-111143. Eun Young-Gyu, Lee Dongjin, Lee Young Chan, Sohn Bo Hwa, Kim Eui Hyun, Yim Sun Young, Kwon Kee Hwan, Lee Ju-Se |
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing. Neural plasticity 2019 2019 7143458. Li Wu, Mei Lingyun, Chen Hongsheng, Cai Xinzhang, Liu Yalan, Men Meichao, Liu Xue Zhong, Yan Denise, Ling Jie, Feng Yo |
The clinical and genetic research of Waardenburg syndrome type I and II in Chinese families. International journal of pediatric otorhinolaryngology 2019 12 130 109806. Liu Qin, Cheng Jing, Lu Yu, Zhou Jia, Wang Li, Yang Changliang, Yang Guang, Yang Hui, Cao Jingyuan, Zhang Zhao, Sun |
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling. Neuroscience letters 2021 04 750 135802. Naushad Shaik Mohammad, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum |
HOXB9 Overexpression Promotes Colorectal Cancer Progression and Is Associated with Worse Survival in Liver Resection Patients for Colorectal Liver Metastases. International journal of molecular sciences 2022 2 23 (4): . Martinou Eirini, Moller-Levet Carla, Karamanis Dimitrios, Bagwan Izhar, Angelidi Angeliki |
Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome. Human genetics 2022 12 142 (3): 419-430. Li Xiaohong, Huang Shasha, Wang Guojian, Kang Dongyang, Han Mingyu, Wu Xiedong, Yang Jinyuan, Zheng Qiuchen, Zhao Chaoyue, Yuan Yongyi, Dai |
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- Page last updated:Apr 22, 2024
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