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Bingxi Chen

Shandong University

15

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420

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Lack of Cul4b, an E3 Ubiquitin Ligase Component, Leads to Embryonic Lethality and Abnormal Placental Development

2012 PLOS ONE
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Serum withdrawal up‐regulates human SIRT1 gene expression in a p53‐dependent manner

2009 Journal of Cellular and Molecular Medicine
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Characterization of Nuclear Localization Signal in the N Terminus of CUL4B and Its Essential Role in Cyclin E Degradation and Cell Cycle Progression

2009 Journal of Biological Chemistry
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Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells.

2009 Experimental Cell Research
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Recurrence of the D100N mutation in a Chinese family with brachydactyly type A1: evidence for a mutational hot spot in the Indian hedgehog gene.

2007 American Journal of Medical Genetics Part A
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Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation

2007 American Journal of Human Genetics
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A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads

2003 American Journal of Medical Genetics Part A
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[Linkage analysis and mutation detection of GRIA3 in Smith--Fineman--Myers syndrome].

2001 Acta Genetica Sinica
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Study on genetic epidemiology of albinism

1994 Acta Genetica Sinica
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Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population

1992 Human Genetics
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