Spontaneous regression of neuroblastoma. - Wikidata - awgldk - TriplyDB

Spontaneous regression of neuroblastoma.

Spontaneous regression of neuroblastoma.

http://www.wikidata.org/entity/Q50156376

about

The oncogenic neurotrophin receptor tropomyosin-related kinase variant, TrkAIII.

P2860

Q55422121-F4A9BD85-77AE-44FB-9EA2-A28641F3E6CA

P2860

Spontaneous regression of neuroblastoma.

http://www.wikidata.org/entity/Q50156376

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Spontaneous regression of neuroblastoma.

@en

Spontaneous regression of neuroblastoma.

@nl

type

label

Spontaneous regression of neuroblastoma.

@en

Spontaneous regression of neuroblastoma.

@nl

prefLabel

Spontaneous regression of neuroblastoma.

@en

Spontaneous regression of neuroblastoma.

@nl

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Q50156376-5C5A0A88-3FD8-41BD-8610-C2D778CEE9CA

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P356

S00441-017-2761-2

P1433

Cell and Tissue Research

P1476

Spontaneous regression of neuroblastoma.

@en

P2093

Garrett M Brodeur

http://www.w3.org/2001/XMLSchema#string

P2860

TrkA alternative splicing: a regulated tumor-promoting switch in human neuroblastoma

Anti-GD2 antibody with GM-CSF, interleukin-2, and isotretinoin for neuroblastoma

Outcome after reduced chemotherapy for intermediate-risk neuroblastoma

Specific association of human telomerase activity with immortal cells and cancer

Terminology and morphologic criteria of neuroblastic tumors: recommendations by the International Neuroblastoma Pathology Committee

An Oncogenic NTRK Fusion in a Patient with Soft-Tissue Sarcoma with Response to the Tropomyosin-Related Kinase Inhibitor LOXO-101

Neurotrophin receptors TrkA and TrkC cause neuronal death whereas TrkB does not

Specific gene expression profiles and chromosomal abnormalities are associated with infant disseminated neuroblastoma.

Molecular basis of spontaneous regression of neuroblastoma: role of neurotrophic signals and genetic abnormalities.

Treatment of high-risk neuroblastoma with intensive chemotherapy, radiotherapy, autologous bone marrow transplantation, and 13-cis-retinoic acid. Children's Cancer Group.

P2888

s00441-017-2761-2

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scholarly article

P356

10.1007/S00441-017-2761-2

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P577

2018-01-05T00:00:00Z

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29305654

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P932

5920563

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