Loss of CDKN1C in a Recurrent Atypical Teratoid/Rhabdoid Tumor.

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Loss of CDKN1C in a Recurrent Atypical Teratoid/Rhabdoid Tumor.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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Loss of CDKN1C in a Recurrent Atypical Teratoid/Rhabdoid Tumor.

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label

Loss of CDKN1C in a Recurrent Atypical Teratoid/Rhabdoid Tumor.

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prefLabel

Loss of CDKN1C in a Recurrent Atypical Teratoid/Rhabdoid Tumor.

@en

P1476

Loss of CDKN1C in a Recurrent Atypical Teratoid/Rhabdoid Tumor.

@en

P2093

Avneesh Gupta

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Carl Koschmann

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Dustin Tran

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Kate Gowans

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Patricia L Robertson

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Rajen Mody

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Sandra Camelo-Piragua

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P2860

Central nervous system atypical teratoid/rhabdoid tumor: results of therapy in children enrolled in a registry

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

Intensive Multimodality Treatment for Children With Newly Diagnosed CNS Atypical Teratoid Rhabdoid Tumor

Imprinted CDKN1C is a tumor suppressor in rhabdoid tumor and activated by restoration of SMARCB1 and histone deacetylase inhibitors

Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.

Genetic ablation of Cyclin D1 abrogates genesis of rhabdoid tumors resulting from Ini1 loss.

Mechanisms by which SMARCB1 loss drives rhabdoid tumor growth.

Alex's Lemonade Stand Foundation Infant and Childhood Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2007-2011.

The SWI/SNF complex--chromatin and cancer.

Alisertib is active as single agent in recurrent atypical teratoid rhabdoid tumors in 4 children.

P31

scholarly article

P356

10.1097/MPH.0000000000000873

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P577

2017-07-20T00:00:00Z

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P698

28731921

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P932

5656519

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