Lista de obras - Yufang Zheng - Dominio Público Uruguay

3' UTR lengthening as a novel mechanism in regulating cellular senescence.

artículo científico publicado en 2018

A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin

artículo científico publicado en 2017

A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population

article

A study in vitro on differentiation of bone marrow mesenchymal stem cells into endometrial epithelial cells in mice

artículo científico publicado en 2011

ADAM17 Is Critical for Multipolar Exit and Radial Migration of Neuronal Intermediate Progenitor Cells in Mice Cerebral Cortex ⬇️

artículo científico publicado el 3 de junio de 2013

Ablation of vacuole protein sorting 18 (Vps18) gene leads to neurodegeneration and impaired neuronal migration by disrupting multiple vesicle transport pathways to lysosomes.

artículo científico publicado en 2012

Analysis and prediction of translation rate based on sequence and functional features of the mRNA.

artículo científico publicado en 2011

Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants

scientific article published on 01 September 2019

Catalytic activity of ADAM28

artículo científico publicado en 2001

Catalytic properties of ADAM19

artículo científico publicado en 2003

DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1

artículo científico publicado en 2008

Dr. Yang Zhong: An explorer on the road forever.

artículo científico publicado en 2017

Enhanced efficacy and specificity of epithelial ovarian carcinogenesis by embedding a DMBA-coated cloth strip in the ovary of rat.

artículo científico publicado en 2012

Evaluation of the contribution of different ADAMs to tumor necrosis factor alpha (TNFalpha) shedding and of the function of the TNFalpha ectodomain in ensuring selective stimulated shedding by the TNFalpha convertase (TACE/ADAM17).

artículo científico publicado en 2004

Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation

artículo científico publicado en 2011

Evidence for regulation of the tumor necrosis factor alpha-convertase (TACE) by protein-tyrosine phosphatase PTPH1

artículo científico publicado en 2002

Evolution and diversity of axon guidance Robo receptor family genes ⬇️

artículo científico publicado en 2020

Expression and purification of the extracellular domain of the human follicle-stimulating hormone receptor using Escherichia coli

artículo científico publicado en 2013

Follicle-stimulating hormone peptide can facilitate paclitaxel nanoparticles to target ovarian carcinoma in vivo

artículo científico publicado en 2009

Formate rescues neural tube defects caused by mutations in Slc25a32

scientific article published on 16 April 2018

Genetic analysis of Wnt/PCP genes in neural tube defects.

artículo científico publicado en 2018

Genetic analysis of rare coding mutations of CELSR1-3 in congenital heart and neural tube defects in Chinese people

artículo científico publicado en 2016

Identification of Functional Mutations in GATA4 in Patients with Congenital Heart Disease ⬇️

artículo científico publicado el 23 de abril de 2013

Length of the ORF, position of the first AUG and the Kozak motif are important factors in potential dual-coding transcripts.

artículo científico publicado en 2010

Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice.

artículo científico publicado en 2018

MAZ mediates the cross-talk between CT-1 and NOTCH1 signaling during gliogenesis

artículo científico publicado en 2016

MIB1 Mutations Reduce Notch Signaling Activation and Contribute to Congenital Heart Disease

scientific article published on 05 December 2018

MicroRNA-197 controls ADAM10 expression to mediate MeCP2's role in the differentiation of neuronal progenitors

artículo científico publicado en 2018

Network correlation analysis revealed potential new mechanisms for neural tube defects beyond folic acid

artículo científico publicado en 2018

Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects

scientific article published on 29 September 2017

Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort

scientific article published on 13 February 2019

Overexpression of sigma-1 receptor inhibits ADAM10 and ADAM17 mediated shedding in vitro.

artículo científico publicado en 2012

Rare mutations of from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling

artículo científico publicado en 2019

SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell.

artículo científico publicado en 2011

Screening of Kozak-motif-located SNPs and analysis of their association with human diseases

artículo científico publicado en 2010

Self-organizing map of gene regulatory networks for cell phenotypes during reprogramming

artículo científico publicado en 2011

Targeted gene silencing using a follicle-stimulating hormone peptide-conjugated nanoparticle system improves its specificity and efficacy in ovarian clear cell carcinoma in vitro

artículo científico publicado en 2013

Targeted paclitaxel nanoparticles modified with follicle-stimulating hormone β 81–95 peptide show effective antitumor activity against ovarian carcinoma ⬇️

artículo científico publicado el 25 de junio de 2013

The piggyBac transposon is an integrating non-viral gene transfer vector that enhances the efficiency of GDEPT.

artículo científico publicado en 2009

Threshold for neural tube defect risk by accumulated singleton loss-of-function variants

artículo científico publicado en 2018

Tumor-directed gene therapy in mice using a composite nonviral gene delivery system consisting of the piggyBac transposon and polyethylenimine

artículo científico publicado en 2009

Variants identified in PTK7 associated with neural tube defects

scientific article published on 28 January 2019

Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population.

artículo científico publicado en 2015

WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways

artículo científico publicado en 2020

Why does the giant panda eat bamboo? A comparative analysis of appetite-reward-related genes among mammals

artículo científico publicado en 2011

Zfp462 deficiency causes anxiety-like behaviors with excessive self-grooming in mice.

artículo científico publicado en 2016

Lista de obras de Yufang Zheng

3' UTR lengthening as a novel mechanism in regulating cellular senescence.

A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin

A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population

A study in vitro on differentiation of bone marrow mesenchymal stem cells into endometrial epithelial cells in mice

ADAM17 Is Critical for Multipolar Exit and Radial Migration of Neuronal Intermediate Progenitor Cells in Mice Cerebral Cortex ⬇️

Ablation of vacuole protein sorting 18 (Vps18) gene leads to neurodegeneration and impaired neuronal migration by disrupting multiple vesicle transport pathways to lysosomes.

Analysis and prediction of translation rate based on sequence and functional features of the mRNA.

Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants

Catalytic activity of ADAM28

Catalytic properties of ADAM19

DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1

Dr. Yang Zhong: An explorer on the road forever.

Enhanced efficacy and specificity of epithelial ovarian carcinogenesis by embedding a DMBA-coated cloth strip in the ovary of rat.

Evaluation of the contribution of different ADAMs to tumor necrosis factor alpha (TNFalpha) shedding and of the function of the TNFalpha ectodomain in ensuring selective stimulated shedding by the TNFalpha convertase (TACE/ADAM17).

Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation

Evidence for regulation of the tumor necrosis factor alpha-convertase (TACE) by protein-tyrosine phosphatase PTPH1

Evolution and diversity of axon guidance Robo receptor family genes ⬇️

Expression and purification of the extracellular domain of the human follicle-stimulating hormone receptor using Escherichia coli

Follicle-stimulating hormone peptide can facilitate paclitaxel nanoparticles to target ovarian carcinoma in vivo

Formate rescues neural tube defects caused by mutations in Slc25a32

Genetic analysis of Wnt/PCP genes in neural tube defects.

Genetic analysis of rare coding mutations of CELSR1-3 in congenital heart and neural tube defects in Chinese people

Identification of Functional Mutations in GATA4 in Patients with Congenital Heart Disease ⬇️

Length of the ORF, position of the first AUG and the Kozak motif are important factors in potential dual-coding transcripts.

Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice.

MAZ mediates the cross-talk between CT-1 and NOTCH1 signaling during gliogenesis

MIB1 Mutations Reduce Notch Signaling Activation and Contribute to Congenital Heart Disease

MicroRNA-197 controls ADAM10 expression to mediate MeCP2's role in the differentiation of neuronal progenitors

Network correlation analysis revealed potential new mechanisms for neural tube defects beyond folic acid

Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects

Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort

Overexpression of sigma-1 receptor inhibits ADAM10 and ADAM17 mediated shedding in vitro.

Rare mutations of from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling

SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell.

Screening of Kozak-motif-located SNPs and analysis of their association with human diseases

Self-organizing map of gene regulatory networks for cell phenotypes during reprogramming

Targeted gene silencing using a follicle-stimulating hormone peptide-conjugated nanoparticle system improves its specificity and efficacy in ovarian clear cell carcinoma in vitro

Targeted paclitaxel nanoparticles modified with follicle-stimulating hormone β 81–95 peptide show effective antitumor activity against ovarian carcinoma ⬇️

The piggyBac transposon is an integrating non-viral gene transfer vector that enhances the efficiency of GDEPT.

Threshold for neural tube defect risk by accumulated singleton loss-of-function variants

Tumor-directed gene therapy in mice using a composite nonviral gene delivery system consisting of the piggyBac transposon and polyethylenimine

Variants identified in PTK7 associated with neural tube defects

Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population.

WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways

Why does the giant panda eat bamboo? A comparative analysis of appetite-reward-related genes among mammals

Zfp462 deficiency causes anxiety-like behaviors with excessive self-grooming in mice.