Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brain.

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IRF2BP2-deficient microglia block the anxiolytic effect of enhanced postnatal care.Dysregulation of the miR-194-CUL4B negative feedback loop drives tumorigenesis in non-small-cell lung carcinoma.Polycomb Repressive Complex 2: Emerging Roles in the Central Nervous System.

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Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brain.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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Lack of CUL4B leads to increas ...... iated by PTGDS in mouse brain.

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Lack of CUL4B leads to increas ...... iated by PTGDS in mouse brain.

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Lack of CUL4B leads to increas ...... iated by PTGDS in mouse brain.

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Lack of CUL4B leads to increas ...... iated by PTGDS in mouse brain.

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Lack of CUL4B leads to increas ...... iated by PTGDS in mouse brain.

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Lack of CUL4B leads to increas ...... iated by PTGDS in mouse brain.

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P1476

Lack of CUL4B leads to increas ...... diated by PTGDS in mouse brain

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P2093

Baichun Jiang

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

Fang Liu

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

Hong Jiang

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

Huili Hu

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

Jupeng Yuan

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

Shuaishuai Lv

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

Shuqian Zhang

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

Wei Zhao

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

Xi Li

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

Yanyan Qian

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P2860

CRL4B catalyzes H2AK119 monoubiquitination and coordinates with PRC2 to promote tumorigenesis

Subventricular zone astrocytes are neural stem cells in the adult mammalian brain

Variants in CUL4B are associated with cerebral malformations

The story of Rett syndrome: from clinic to neurobiology

Purification and chemical characterization of beta-trace protein from human cerebrospinal fluid: its identification as prostaglandin D synthase

Essential role of the CUL4B ubiquitin ligase in extra-embryonic tissue development during mouse embryogenesis

Rescue of the genetically engineered Cul4b mutant mouse as a potential model for human X-linked mental retardation

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor

Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation

Ezh2, the histone methyltransferase of PRC2, regulates the balance between self-renewal and differentiation in the cerebral cortex

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10.1093/HMG/DDV200

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2015-05-29T00:00:00Z

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26025376

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Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brain.

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P2860

P2860

Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brain.

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