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Lack of Cul4b, an E3 ubiquitin ligase component, leads to embryonic lethality and abnormal placental development

PloS one, 2012-05, Vol.7 (5), p.e37070

2012

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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

The Journal of biological chemistry, 2009-11, Vol.284 (48), p.33320-33332

2009

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Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation

American journal of human genetics, 2007-03, Vol.80 (3), p.561-566

2007

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

Journal of cellular and molecular medicine, 2009-10, Vol.13 (10), p.4176-4184

2009

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A Novel Multi-Ensemble Method for Identifying Essential Proteins

Journal of computational biology, 2021-07, Vol.28 (7), p.637-649

2021

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Removal notice to "Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells" [YEXCR Volume 315, Issue 17, 15 October 2009, Pages 2953-2962]

Experimental cell research, 2021-07, p.112609

2021

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Retraction notice to “Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells” [YEXCR Volume 315, Issue 17, 15 October 2009, Pages 2953–2962]

Experimental cell research, 2021-07, Vol.404 (1), p.112609, Article 112609

2021

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Removal notice to "Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells" YEXCR Volume 315, Issue 17, 15 October 2009, Pages 2953-2962

Experimental cell research, 2021-07, Vol.404 (1), p.112609

2021

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RETRACTED: Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells

Experimental cell research, 2009-10, Vol.315 (17), p.2953-2962

2009

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Multi-View Geometry Based Visual Perception and Control of Robotic Systems

1, 2018

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Sp1 and CREB regulate basal transcription of the human SNF2L gene

Biochemical and biophysical research communications, 2008-04, Vol.368 (2), p.438-444

2008

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Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells

Experimental cell research, 2009-10, Vol.315 (17), p.2953-2962

2009

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A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads

American journal of medical genetics, 2003-07, Vol.120A (3), p.345-349

2003

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Transformer State Awareness Technology Based on Multi-Kernel SVM

2024 3rd International Conference on Energy, Power and Electrical Technology (ICEPET), 2024, p.1851-1854

2024

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Fault Protection of Small Resistance Grounding System Based on Zero Sequence Voltage-Current Waveform Comparison Coefficient

2023 10th International Forum on Electrical Engineering and Automation (IFEEA), 2023, p.715-720

2023

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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

American journal of medical genetics. Part A, 2007-06, Vol.143A (11), p.1246-1248

2007

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Research letter. Recurrence of the d100n mutation in a chinese family with brachydactyly type A1: Evidence for a mutational hot spot in the Indian Hedgehog gene

American journal of medical genetics. Part A, 2007, Vol.143 (11), p.1246-1248

2007

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A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3

American journal of medical genetics. Part A, 2004-09, Vol.129A (3), p.286-289

2004

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The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans

Zhonghua yi xue yi chuan xue za zhi, 2002-08, Vol.19 (4), p.295

2002

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Genomic structure of low density lipoprotein receptor related protein 5 gene

Zhonghua yi xue yi chuan xue za zhi, 2002-12, Vol.19 (6), p.467

2002

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Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome

Zhonghua yi xue yi chuan xue za zhi, 2002-02, Vol.19 (1), p.22

2002

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Gene mapping of a nonsyndromic hearing impairmint family

Zhonghua yi xue yi chuan xue za zhi, 2003-04, Vol.20 (2), p.89

2003

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Smith-fineman-myers syndrome:Report on a large family

American journal of medical genetics, 1993-09, Vol.47 (3), p.307-311

1993

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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

Human genetics, 1992-09, Vol.90 (1-2), p.149-150

1992

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A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3

American journal of medical genetics, 2004, Vol.129A (3), p.286-289

2004

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Lack of Cul4b, an E3 ubiquitin ligase component, leads to embryonic lethality and abnormal placental development

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

Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation

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

A Novel Multi-Ensemble Method for Identifying Essential Proteins

Removal notice to "Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells" [YEXCR Volume 315, Issue 17, 15 October 2009, Pages 2953-2962]

Retraction notice to “Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells” [YEXCR Volume 315, Issue 17, 15 October 2009, Pages 2953–2962]

Removal notice to "Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells" YEXCR Volume 315, Issue 17, 15 October 2009, Pages 2953-2962

RETRACTED: Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells

Multi-View Geometry Based Visual Perception and Control of Robotic Systems

Sp1 and CREB regulate basal transcription of the human SNF2L gene

Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells

A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads

Transformer State Awareness Technology Based on Multi-Kernel SVM

Fault Protection of Small Resistance Grounding System Based on Zero Sequence Voltage-Current Waveform Comparison Coefficient

Recurrence of the D100N mutation in a Chinese family with brachydactyly type A1: Evidence for a mutational hot spot in the Indian hedgehog gene

Research letter. Recurrence of the d100n mutation in a chinese family with brachydactyly type A1: Evidence for a mutational hot spot in the Indian Hedgehog gene

A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3

The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans

Genomic structure of low density lipoprotein receptor related protein 5 gene

Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome

Gene mapping of a nonsyndromic hearing impairmint family

Smith-fineman-myers syndrome:Report on a large family

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

A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3

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