[1] |
Orr BA. Pathology, diagnostics, and classification of medulloblastoma[J]. Brain Pathol, 2020, 30: 664-678.
|
[2] |
漆松涛. 重视我国小儿神经外科的建设与发展[J]. 中华神经外科杂志, 2019, 35: 757-759.
|
[3] |
Roussel MF, Stripay JL. Modeling pediatric medulloblastoma[J]. Brain Pathol, 2020, 30: 703-712.
|
[4] |
马磊, 陈维英, 施又丹, 等. 原花青素对髓母细胞瘤Daoy细胞增殖和凋亡的影响[J]. 基础医学与临床, 2015, 35: 929-933.
|
[5] |
Ballabio C, Anderle M, Gianesello M, et al. Modeling medulloblastoma in vivo and with human cerebellar organoids[J]. Nat Commun, 2020, 11: 583. doi: 10.1038/s41467-019-13989-3.
|
[6] |
Dietl S, Schwinn S, Dietl S, et al. MB3W1 is an orthotopic xenograft model for anaplastic medulloblastoma displaying cancer stem cell- and group 3-properties[J]. BMC Cancer, 2016, 16: 115. doi: 10.1186/s12885-016-2170-z.
|
[7] |
Badodi S, Marino S, Guglielmi L. Establishment and culture of patient-derived primary medulloblastoma cell lines[J]. Methods Mol Biol, 2019, 1869: 23-36.
|
[8] |
Shiraishi R, Kawauchi D. Epigenetic regulation in medulloblastoma pathogenesis revealed by genetically engineered mouse models[J]. Cancer Sci, 2021, 112: 2948-2957.
|
[9] |
Ramaswamy V, Remke M, Bouffet E, et al. Risk stratification of childhood medulloblastoma in the molecular era: the current consensus[J]. Acta Neuropathol, 2016, 131: 821-831.
|
[10] |
Qi L, Kogiso M, Du Y, et al. Impact of SCID mouse gender on tumorigenicity, xenograft growth and drug-response in a large panel of orthotopic PDX models of pediatric brain tumors[J]. Cancer Lett, 2020, 493: 197-206.
|
[11] |
Okada S, Vaeteewoottacharn K, Kariya R. Application of highly immunocompromised mice for the establishment of patient-derived xenograft (PDX) models[J]. Cells, 2019, 8:889. doi: 10.3390/cells8080889
|
[12] |
Ben-david U, Ha G, Tseng YY, et al. Patient-derived xenografts undergo mouse-specific tumor evolution[J]. Nat Genet, 2017, 49: 1567-1575.
|