Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and ATP7A[original query] |
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| Copper transporting P-type ATPases and human disease. Journal of bioenergetics and biomembranes 2003 1 34 (5): 333-8. Cox Diane W, Moore Steven D |
| A Drosophila model of Menkes disease reveals a role for DmATP7 in copper absorption and neurodevelopment. Disease models & mechanisms 2009 12 3 (1-2): 84-91. Bahadorani Sepehr, Bahadorani Peyman, Marcon Edyta, Walker David W, Hilliker Arthur |
| Polymorphisms of metal transporter genes DMT1 and ATP7A in Wilson's disease. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) 2014 Jan 28 (1): 8-12. Przyby?kowski Adam, Gromadzka Gra?yna, Cz?onkowska An |
| Clinical outcome of cisplatin-based chemotherapy is associated with the polymorphisms of GSTP1 and XRCC1 in advanced non-small cell lung cancer patients. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2015 Sep 17 (9): 720-6. Deng J-H, Deng J, Shi D-H, Ouyang X-N, Niu P |
| Use of Germline Genetic Variability for Prediction of Chemoresistance and Prognosis of Breast Cancer Patients. Cancers 2018 12 10 (12): . Hlavac Viktor, Kovacova Maria, Elsnerova Katerina, Brynychova Veronika, Kozevnikovova Renata, Raus Karel, Kopeckova Katerina, Mestakova Sona, Vrana David, Gatek Jiri, Ostasov Pavel, Vaclavikova Radka, Soucek Pav |
| ATP7A mutations in 66 Japanese patients with Menkes disease and carrier detection: A gene analysis. Pediatrics international : official journal of the Japan Pediatric Society 2019 2 61 (4): 345-350. Fujisawa Chie, Kodama Hiroko, Hiroki Tomoko, Akasaka Yoshikiyo, Hamanoue Mako |
| Osseous Metaplasia in a Bladder Diverticulum in a Patient with Mosaic Menkes Disease. Urology 2019 11 136 238-240. Canalichio Katie L, Chisholm Karen M, Lendvay Thomas |
| Cortical copper transporter expression in schizophrenia: interactions of risk gene dysbindin-1. Journal of neural transmission (Vienna, Austria : 1996) 2021 4 128 (5): 701-709. Schoonover Kirsten E, Kennedy William M, Roberts Rosalinda |
| Genotype frequency of ATP7A and ATP7B mutation-related copper-associated hepatitis in a Japanese guide dog Labrador retriever population. The Journal of veterinary medical science 2021 11 84 (1): 16-19. Takanosu Masamine, Suzuki Katsus |
| Association of SLC11A1 polymorphisms with anthropometric and biochemical parameters describing Type 2 Diabetes Mellitus. Scientific reports 2023 4 13 (1): 6195. Kavian Zahra, Sargazi Saman, Majidpour Mahdi, Sarhadi Mohammad, Saravani Ramin, Shahraki Mansour, Mirinejad Shekoufeh, Heidari Nia Milad, Piri Mary |
| Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 10 1-11. Cathrine Goberg Olsen, Øyvind Løvold Busk, Øystein Lunde Holla, Kristian Tveten, Trygve Holmøy, Ole-Bjørn Tysnes, Helle Høy |
| ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of inherited metabolic disease 2023 1 46 (2): 163-173. De Feyter S, Beyens A, Callewaert |
| Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population. American journal of medical genetics. Part A 2024 10 e63914. Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, Selinda Mascarenhas, Lakshmi Priya Rao, Karthik Vijay Nair, Bhagesh Hunakunti, Adarsh Pooradan Prasannakumar, Rohit Naik, Dhanya Lakshmi Narayanan, Shalini S Nayak, Vivekananda Bhat, Suvasini Sharma, Y Ramesh Bhat, B L Yatheesha, Rajesh Kulkarni, Siddaramappa J Patil, Sheela Nampoothiri, Shahyan Siddiqui, Katta Mohan Girisha, Stephanie Bielas, Anju Shuk |
- Page last reviewed:Feb 1, 2024
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