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Ana Meireles - Publications

Affiliations: 
Stanford University, Palo Alto, CA 
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Iyer H, Shen K, Meireles AM, Talbot WS. A lysosomal regulatory circuit essential for the development and function of microglia. Science Advances. 8: eabp8321. PMID 36044568 DOI: 10.1126/sciadv.abp8321  0.607
2022 Lysko DE, Meireles AM, Folland C, McNamara E, Laing NG, Lamont PJ, Ravenscroft G, Talbot WS. Partial loss-of-function variant in neuregulin 1 identified in family with heritable peripheral neuropathy. Human Mutation. PMID 35485770 DOI: 10.1002/humu.24393  0.694
2021 Heller IS, Guenther CA, Meireles AM, Talbot WS, Kingsley DM. Characterization of mouse Bmp5 regulatory injury element in zebrafish wound models. Bone. 116263. PMID 34826632 DOI: 10.1016/j.bone.2021.116263  0.496
2018 Meireles AM, Shen K, Zoupi L, Iyer H, Bouchard EL, Williams A, Talbot WS. The Lysosomal Transcription Factor TFEB Represses Myelination Downstream of the Rag-Ragulator Complex. Developmental Cell. 47: 319-330.e5. PMID 30399334 DOI: 10.1016/J.Devcel.2018.10.003  0.348
2015 Ravenscroft G, Nolent F, Rajagopalan S, Meireles AM, Paavola KJ, Gaillard D, Alanio E, Buckland M, Arbuckle S, Krivanek M, Maluenda J, Pannell S, Gooding R, Ong RW, Allcock RJ, et al. Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita. American Journal of Human Genetics. 96: 955-61. PMID 26004201 DOI: 10.1016/J.Ajhg.2015.04.014  0.677
2015 Shiau CE, Kaufman Z, Meireles AM, Talbot WS. Differential requirement for irf8 in formation of embryonic and adult macrophages in zebrafish. Plos One. 10: e0117513. PMID 25615614 DOI: 10.1371/journal.pone.0117513  0.563
2015 Ravenscroft G, Nolent F, Rajagopalan S, Meireles A, Paavola K, Gaillard D, Alanio E, Buckland M, Arbuckle S, Krivanek M, Maluenda J, Pannell S, Gooding R, Ong R, Allcock R, et al. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita Neuromuscular Disorders. 25. DOI: 10.1016/J.Nmd.2015.06.013  0.576
2014 Meireles AM, Shiau CE, Guenther CA, Sidik H, Kingsley DM, Talbot WS. The phosphate exporter xpr1b is required for differentiation of tissue-resident macrophages. Cell Reports. 8: 1659-67. PMID 25220463 DOI: 10.1016/J.Celrep.2014.08.018  0.589
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