Human Genome Epidemiology Literature Finder
|
Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and RTN4R[original query] |
|---|
| Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth. The Journal of neuroscience : the official journal of the Society for Neuroscience 2008 Dec 28 (49): 13161-72. Budel Stéphane, Padukkavidana Thihan, Liu Betty P, Feng Zeny, Hu Fenghua, Johnson Sam, Lauren Juha, Park James H, McGee Aaron W, Liao Ji, Stillman Althea, Kim Ji-Eun, Yang Bao-Zhu, Sodi Stefano, Gelernter Joel, Zhao Hongyu, Hisama Fuki, Arnsten Amy F T, Strittmatter Stephen |
| Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling. Molecular genetics & genomic medicine 2016 Jul 4 (4): 447-56. Thomas Rhalena A, Ambalavanan Amirthagowri, Rouleau Guy A, Barker Philip |
| Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine. Brain sciences 2019 12 10 (1): . Smedfors Gabriella, Liesecke Franziska, Ran Caroline, Olson Lars, Karlsson Tobias E, Carmine Belin Andr |
| A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders. Current Alzheimer research 2020 Nov . El Bitar Fadia, Al Sudairy Nourah, Qadi Najeeb, Al Rajeh Saad, Alghamdi Fatimah, Al Amari Hala, Al Dawsari Ghadeer, Alsubaie Sahar, Al Sudairi Mishael, Abdulaziz Sara, Al Tassan Na |
| An in-depth analysis reveals two new genetic variants on 22q11.2 associated with vitiligo in the Chinese Han population. Molecular biology reports 2021 Aug . Tang Xianfa, Cheng Hui, Cheng Lu, Liang Bo, Chen Mengyun, Zheng Xiaodong, Xiao Feng |
- Page last reviewed:Feb 1, 2024
- Content source:

