Human Genome Epidemiology Literature Finder
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Query Trace: CSF1R[original query] |
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Association between CSF1 and CSF1R Polymorphisms and Parkinson's Disease in Taiwan. Journal of clinical medicine 2019 Sep 8 (10): . Chang Kuo-Hsuan, Wu Yih-Ru, Chen Yi-Chun, Wu Hsiu-Chuan, Chen Chiung-M |
Genetic analyses of early-onset Alzheimer's disease using next generation sequencing. Scientific reports 2019 6 9 (1): 8368. Giau Vo Van, Bagyinszky Eva, Yang Young Soon, Youn Young Chul, An Seong Soo A, Kim Sang Y |
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 2019 12 5 (6): . Cochran J Nicholas, McKinley Emily C, Cochran Meagan, Amaral Michelle D, Moyers Bryan A, Lasseigne Brittany N, Gray David E, Lawlor James M J, Prokop Jeremy W, Geier Ethan G, Holt James M, Thompson Michelle L, Newberry J Scott, Yokoyama Jennifer S, Worthey Elizabeth A, Geldmacher David S, Love Marissa Natelson, Cooper Gregory M, Myers Richard M, Roberson Erik |
Activating mutations in CSF1R and additional receptor tyrosine kinases in histiocytic neoplasms. Nature medicine 2019 11 25 (12): 1839-1842. Durham Benjamin H, Lopez Rodrigo Estibaliz, Picarsic Jennifer, Abramson David, Rotemberg Veronica, De Munck Steven, Pannecoucke Erwin, Lu Sydney X, Pastore Alessandro, Yoshimi Akihide, Mandelker Diana, Ceyhan-Birsoy Ozge, Ulaner Gary A, Walsh Michael, Yabe Mariko, Petrova-Drus Kseniya, Arcila Maria E, Ladanyi Marc, Solit David B, Berger Michael F, Hyman David M, Lacouture Mario E, Erickson Caroline, Saganty Ruth, Ki Michelle, Dunkel Ira J, Santa-María López Vicente, Mora Jaume, Haroche Julien, Emile Jean-Francois, Decaux Olivier, Geissmann Frederic, Savvides Savvas N, Drilon Alexander, Diamond Eli L, Abdel-Wahab Om |
Pathway Mutations in Breast Cancer Using Whole-Exome Sequencing. Oncology research 2019 Oct . Chang Ya-Sian, Chang Chieh-Min, Lin Chien-Yu, Chao Dy-San, Huang Hsi-Yuan, Chang Jan-Gow |
Polymorphisms of CSF1R and WISP1 genes are associated with severity of familial adenomatous polyposis in APC pigs. Gene 2020 7 759 144988. Sikorska Agata, Stachowiak Monika, Flisikowska Tatiana, Stachecka Joanna, Flisikowski Krzysztof, Switonski Mar |
Trem2 deficiency differentially affects phenotype and transcriptome of human APOE3 and APOE4 mice. Molecular neurodegeneration 2020 7 15 (1): 41. Fitz Nicholas F, Wolfe Cody M, Playso Brittany E, Biedrzycki Richard J, Lu Yi, Nam Kyong Nyon, Lefterov Iliya, Koldamova Radosve |
Transcriptomic silencing as a potential mechanism of treatment resistance. JCI insight 2020 6 5 (11): . Adashek Jacob J, Kato Shumei, Parulkar Rahul, Szeto Christopher W, Sanborn J Zachary, Vaske Charles J, Benz Stephen C, Reddy Sandeep K, Kurzrock Razel |
Adamantinomatous Craniopharyngioma in an Adult: A Case Report with NGS Analysis. International medical case reports journal 2020 5 13 123-137. Jastania Raid A, Saeed Muhammad, Al-Khalidi Hisham, AlQuthami Khalid, Nageeti Tahani H, Al-Allaf Faisal A, Valerie Kristoffer, Taher Mohiuddin |
Relationships between novel nucleotide variants within the colony-stimulating factor 1 receptor (CSF1R) gene and mastitis indicators in sheep. Animal biotechnology 2020 10 33 (4): 731-738. Hu Huina, Yang Yuta, Lan Xianyong, Zhang Qingfeng, Pan Chuanyi |
The third case of TNFRSF11A-associated dysosteosclerosis with a mutation producing elongating proteins. Journal of human genetics 2020 10 66 (4): 371-377. Xue Jing-Yi, Wang Zheng, Smithson Sarah F, Burren Christine P, Matsumoto Naomichi, Nishimura Gen, Ikegawa Shiro, Guo Lo |
Evaluation of CSF1R-related adult onset leukoencephalopathy with axonal spheroids and pigmented glia diagnostic criteria. European journal of neurology 2021 9 29 (1): 329-334. Ayrignac Xavier, Carra-Dallière Clarisse, Codjia Pekes, Mouzat Kevin, Castelnovo Giovanni, Ellie Emmanuel, Etcharry-Bouyx Frédérique, Belliard Serge, Marelli Cecilia, Portet Florence, Le Ber Isabelle, Durand-Dubief Francoise, Mathey Guillaume, Stankoff Bruno, Dorboz Imen, Drunat Severine, Boespflug-Tanguy Odile, Menjot de Champfleur Nicolas, Lumbroso Serge, Mochel Fanny, Labauge Pier |
Rare Modifier Variants Alter the Severity of Cardiovascular Disease in Pseudoxanthoma Elasticum: Identification of Novel Candidate Modifier Genes and Disease Pathways Through Mixture of Effects Analysis. Frontiers in cell and developmental biology 2021 6 9 612581. De Vilder Eva Y G, Martin Ludovic, Lefthériotis Georges, Coucke Paul, Van Nieuwerburgh Filip, Vanakker Olivier |
Multimodal single-cell/nucleus RNA sequencing data analysis uncovers molecular networks between disease-associated microglia and astrocytes with implications for drug repurposing in Alzheimer's disease. Genome research 2021 2 31 (10): 1900-1912. Xu Jielin, Zhang Pengyue, Huang Yin, Zhou Yadi, Hou Yuan, Bekris Lynn M, Lathia Justin, Chiang Chien-Wei, Li Lang, Pieper Andrew A, Leverenz James B, Cummings Jeffrey, Cheng Feixio |
High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystrophy. Frontiers in neurology 2021 12 631407. Chen Zhiyong, Tan Yi Jayne, Lian Michelle M, Tandiono Moses, Foo Jia Nee, Lim Weng Khong, Kandiah Nagaendran, Tan Eng-King, Ng Adeline S |
CD40 Pathway and IL-2 Expression Mediate the Differential Outcome of Colorectal Cancer Patients with Different CSF1R c.1085 Genotypes. International journal of molecular sciences 2021 11 22 (22): . Yeh Yu-Min, Lin Peng-Chan, Su Wu-Chou, Shen Meng- |
Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations. Annals of clinical and translational neurology 2021 10 8 (11): 2121-2131. Tsai Pei-Chien, Fuh Jong-Ling, Yang Chih-Chao, Chang Anna, Lien Li-Ming, Wang Pei-Ning, Lai Kuan-Lin, Tsai Yu-Shuen, Lee Yi-Chung, Liao Yi-C |
A case of CSF1R-related leukoencephalopathy: serial neuroimaging and neuropsychological tests. Neurocase 2021 10 27 (5): 415-418. Sohn Eun Hee, Lee Juyoun, Lee Ae Young, Shin Jin-Ho |
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
Genetic landscape of early-onset dementia in Hungary. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Jun . Csaban Dora, Illes Anett, Renata Toth-Bencsik, Balicza Peter, Pentelenyi Klara, Molnar Viktor, Gezsi Andras, Grosz Zoltan, Gal Aniko, Kovacs Tibor, Klivenyi Peter, Molnar Maria Jud |
Next-Generation Sequencing in Lung Cancer Patients: A Comparative Approach in NSCLC and SCLC Mutational Landscapes. Journal of personalized medicine 2022 3 12 (3): . Pop-Bica Cecilia, Ciocan Cristina Alexandra, Braicu Cornelia, Harangu? Antonia, Simon Marioara, Nutu Andreea, Pop Laura Ancuta, Slaby Ondrej, Atanasov Atanas G, Pirlog Radu, Al Hajjar Nadim, Berindan-Neagoe Ioa |
Mutation Profiling of Intracranial Myxopapillary Ependymoma by Next Generation DNA Sequencing. The Gulf journal of oncology 2022 2 1 (37): 7-16. Taher Mohiuddin M, Alhussini Abdulaziz Abdulnasser, Saeed Muhammad, Athar Mohammad, Bantan Najwa Abdalkabeer A, Jastania Raid A, Balkhoyour Kamal Bakour, Nageeti Tahani |
Hematopoietic Stem Cell Transplantation in CSF1R-Related Leukoencephalopathy: Retrospective Study on Predictors of Outcomes. Pharmaceutics 2022 12 14 (12): . Dulski Jaros?aw, Heckman Michael G, White Launia J, ?ur-Wyrozumska Kamila, Lund Troy C, Wszolek Zbigniew |
The genetic and phenotypic spectra of adult genetic leukoencephalopathies in a cohort of 309 patients. Brain : a journal of neurology 2022 11 . Wu Chujun, Wang Mengwen, Wang Xingao, Li Wei, Li Shaowu, Chen Bin, Niu Songtao, Tai Hongfei, Pan Hua, Zhang Zaiqia |
CSF1R regulates schizophrenia-related stress response and vascular association of microglia/macrophages. BMC medicine 2023 8 21 (1): 286. Ling Yan, Yanli Li, Fengmei Fan, Mengzhuang Gou, Fangling Xuan, Wei Feng, Keerthana Chithanathan, Wei Li, Junchao Huang, Hongna Li, Wenjin Chen, Baopeng Tian, Zhiren Wang, Shuping Tan, Alexander Zharkovsky, L Elliot Hong, Yunlong Tan, Li Ti |
Gene mutation profiling and clinical significances in patients with renal cell carcinoma. Clinics (Sao Paulo, Brazil) 2023 7 78 100259. Yongquan Wang, Peng He, Xiaozhou Zhou, Cong Wang, Jian Fu, Dawei Zhang, Deyang Liao, Zhansong Zhou, Chunman Wu, Wei Go |
Novel partial deletions, frameshift and missense mutations of CSF1R in patents with CSF1R-related leukoencephalopathy. European journal of neurology 2023 3 . Ishiguro Takanobu, Konno Takuya, Hara Norikazu, Zhu Bin, Okada Satoshi, Shibata Mamoru, Saika Reiko, Kitano Takaya, Toko Megumi, Nezu Tomohisa, Hama Yuka, Kawazoe Tomoya, Takahashi-Iwata Ikuko, Yabe Ichiro, Sato Kota, Takeda Hayato, Toda Shintaro, Nishimiya Jin, Teduka Toshiyuki, Nozaki Hiroaki, Kasuga Kensaku, Miyashita Akinori, Onodera Osamu, Ikeuchi Takes |
Whole-exome sequencing reveals genetic variants in low-risk and high-risk neuroblastoma. Gene 2023 2 860 147233. Altun Zekiye, Yuan Hongling, Baran Burçin, Akta? Safiye, Sönmez Esra Esmeray, Küçük Can, Olgun N |
Identifying survival of pan-cancer patients under immunotherapy using genomic mutation signature with large sample cohorts. Journal of molecular medicine (Berlin, Germany) 2023 11 . Liuchao Zhang, Yuanyuan Wang, Liuying Wang, Meng Wang, Shuang Li, Jia He, Jianxin Ji, Kang Li, Lei C |
Somatic cancer driver mutations are enriched and associated with inflammatory states in Alzheimer's disease microglia. bioRxiv : the preprint server for biology 2024 1 . August Yue Huang, Zinan Zhou, Maya Talukdar, Michael B Miller, Brian Chhouk, Liz Enyenihi, Ila Rosen, Edward Stronge, Boxun Zhao, Dachan Kim, Jaejoon Choi, Sattar Khoshkhoo, Junho Kim, Javier Ganz, Kyle Travaglini, Mariano Gabitto, Rebecca Hodge, Eitan Kaplan, Ed Lein, Philip L De Jager, David A Bennett, Eunjung Alice Lee, Christopher A Wal |
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- Page last updated:Apr 16, 2024
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