| Dissecting the regulatory strategies of NF-κB RelA target genes in the inflammatory response reveals differential transactivation logics KA Ngo, K Kishimoto, J Davis-Turak, A Pimplaskar, Z Cheng, R Spreafico, ... Cell reports 30 (8), 2758-2775. e6, 2020 | 61 | 2020 |
| Dormant spores sense amino acids through the B subunits of their germination receptors L Artzi, A Alon, KP Brock, AG Green, A Tam, FH Ramírez-Guadiana, ... Nature Communications 12 (1), 6842, 2021 | 33 | 2021 |
| MaveDB v2: a curated community database with over three million variant effects from multiplexed functional assays AF Rubin, JK Min, NJ Rollins, EY Da, D Esposito, M Harrington, J Stone, ... Biorxiv, 2021.11. 29.470445, 2021 | 15 | 2021 |
| Plasma neurofilament light chain is elevated in adaptor protein complex 4‐related hereditary spastic paraplegia JE Alecu, A Saffari, M Ziegler, C Jordan, A Tam, S Kim, E Leung, ... Movement Disorders 38 (9), 1742-1750, 2023 | 8 | 2023 |
| The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation S Luo, S Rollins, K Schmitz-Abe, A Tam, Q Li, J Shi, J Lin, R Wang, ... Clinica Chimica Acta, 119765, 2024 | 1 | 2024 |
| The spectrum of movement disorders in young children with ARX‐related epilepsy‐dyskinesia syndrome SK Akula, V Quiroz, AM D'Gama, MY Chiu, HY Koh, A Saffari, Z Zaman, ... Annals of Clinical and Translational Neurology, 2024 | 1 | 2024 |
| Deep Brain Stimulation For Medically-Refractory Status Dystonicus in UBA5-related Disorder Z Zaman, N Straka, AL Pinto, R Srouji, A Tam, U Periasamy, S Stone, ... Movement disorders: official journal of the Movement Disorder Society 38 (9 …, 2023 | 1 | 2023 |
| Juvenile‐onset Huntington's disease–Spectrum and evolution of presenting movement disorders K Yang, V Quiroz, A Tam, R Srouji, X Villanueva, C Amarales, ... Annals of Clinical and Translational Neurology, 2024 | | 2024 |
| Biallelic variants in RINT1 present as early-onset pure hereditary spastic paraplegia V Quiroz, L Planas-Serra, A Sveden, A Tam, HM Kim, U Zubair, D Resch, ... The Journal of Clinical Investigation 134 (17), 2024 | | 2024 |
| Case Report of Friedreich's Ataxia and ALG1‐Related Biochemical Abnormalities in a Patient With Progressive Spastic Paraplegia A Quinlan, L Rodan, E Barkoudah, A Tam, A Saffari, I Shammas, ... American Journal of Medical Genetics Part A, e63890, 2024 | | 2024 |
| Expanding the Clinical and Genetic Spectrum of RAB3GAP1-Related Disorders with Novel Movement Disorders ML Wiese, A Saffari, R Kaiyrzhanov, PN Torbati, EG Karimiani, M Zamani, ... Neuropediatrics 54 (S 01), A-236, 2023 | | 2023 |
| Supporting Data A Tam, S Kim, E Leung, K Szczaluba, H Mierzewska, SD King, ... Eur J Paediatr Neurol 22 (2), 308-315, 2018 | | 2018 |
| Biallelic Variants in COQ4 Cause Childhood‐Onset Pure Hereditary Spastic Paraplegia L Schierbaum, V Quiroz, A Tam, U Zubair, L Tochen, R Srouji, K Yang, ... Movement Disorders Clinical Practice, 0 | | |
Alexander HoffmannUCLA在 ucla.edu 的电子邮件经过验证
