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Physiological and transcriptional variations inducing complex adaptive mechanisms in grapevine by salt stress

Environmental and experimental botany, 2019-06, Vol.162, p.455-467

2019

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Fumonisin B1 as a Tool to Explore Sphingolipid Roles in Arabidopsis Primary Root Development

International journal of molecular sciences, 2022-11, Vol.23 (21), p.12925

2022

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Identification of novel FBN1 variations implicated in congenital scoliosis

Journal of human genetics, 2020-03, Vol.65 (3), p.221-230

2020

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TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

Human molecular genetics, 2019-02, Vol.28 (4), p.539-547

2019

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Three patterns of osteoarticular involvement in SAPHO syndrome: a cluster analysis based on whole body bone scintigraphy of 157 patients

Rheumatology (Oxford, England), 2019-06, Vol.58 (6), p.1047-1055

2019

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Quadruple valve replacement for patient with infective endocarditis 16 years after Fallot's Tetralogy Repair procedure: A case report

Heliyon, 2024-01, Vol.10 (1), p.e23351, Article e23351

2024

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Exocyst subunit SEC3A marks the germination site and is essential for pollen germination in Arabidopsis thaliana

Scientific reports, 2017-01, Vol.7 (1), p.40279-40279, Article 40279

2017

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Genome-wide identification, characterization and expression analysis of HAK genes and decoding their role in responding to potassium deficiency and abiotic stress in Medicago truncatula

PeerJ (San Francisco, CA), 2022-09, Vol.10, p.e14034, Article e14034

2022

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Arabidopsis COG Complex Subunits COG3 and COG8 Modulate Golgi Morphology, Vesicle Trafficking Homeostasis and Are Essential for Pollen Tube Growth

PLoS genetics, 2016-07, Vol.12 (7), p.e1006140-e1006140

2016

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Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis

Frontiers in bioengineering and biotechnology, 2019-12, Vol.7, p.364-364

2019

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Arabidopsis EXO70A1 recruits Patellin3 to the cell membrane independent of its role as an exocyst subunit

Journal of integrative plant biology, 2017-12, Vol.59 (12), p.851-865

2017

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Hawthorn Polyphenol Extract Inhibits UVB-Induced Skin Photoaging by Regulating MMP Expression and Type I Procollagen Production in Mice

Journal of agricultural and food chemistry, 2018-08, Vol.66 (32), p.8537-8546

2018

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Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1023-n/a

2020

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WeChat App in the follow up of thyroid cancer patients after thyroidectomy during the COVID‐19 pandemic

British journal of surgery, 2020-10, Vol.107 (11), p.e533-e533

2020

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Lonicera caerulea Berry Polyphenols Activate SIRT1, Enhancing Inhibition of Raw264.7 Macrophage Foam Cell Formation and Promoting Cholesterol Efflux

Journal of agricultural and food chemistry, 2019-06, Vol.67 (25), p.7157-7166

2019

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Inhibition of ribosome biogenesis by actinomycin D affects Arabidopsis root development

Biochemical and biophysical research communications, 2022-01, Vol.588, p.61-67

2022

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The study of integrated care strategies to prevent low birth weight children gastrointestinal disease

AIP Conference Proceedings, 2021, Vol.2350 (1)

2021

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Protective effects of hawthorn (Crataegus pinnatifida) polyphenol extract against UVB‐induced skin damage by modulating the p53 mitochondrial pathway in vitro and in vivo

Journal of food biochemistry, 2019-02, Vol.43 (2), p.e12708-n/a

2019

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Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

Journal of medical genetics, 2021-01, Vol.58 (1), p.41-47

2021

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The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

Human genetics, 2018-07, Vol.137 (6-7), p.553-567

2018

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TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model

Genetics in medicine, 2019-07, Vol.21 (7), p.1548-1558

2019

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Genetic Polymorphism of LBX1 Is Associated With Adolescent Idiopathic Scoliosis in Northern Chinese Han Population

Spine (Philadelphia, Pa. 1976), 2017-08, Vol.42 (15), p.1125-1129

2017

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Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome

Kidney international, 2020-10, Vol.98 (4), p.1020-1030

2020

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A single cohort, open-label study of the efficacy of pamidronate for palmoplantar pustulosis in synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome

Clinical and experimental rheumatology, 2020-11, Vol.38 (6), p.1263

2020

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TBX6 missense variants expand the mutational spectrum in a non‐Mendelian inheritance disease

Human mutation, 2020-01, Vol.41 (1), p.182-195

2020

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Physiological and transcriptional variations inducing complex adaptive mechanisms in grapevine by salt stress

Fumonisin B1 as a Tool to Explore Sphingolipid Roles in Arabidopsis Primary Root Development

Identification of novel FBN1 variations implicated in congenital scoliosis

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

Three patterns of osteoarticular involvement in SAPHO syndrome: a cluster analysis based on whole body bone scintigraphy of 157 patients

Quadruple valve replacement for patient with infective endocarditis 16 years after Fallot's Tetralogy Repair procedure: A case report

Exocyst subunit SEC3A marks the germination site and is essential for pollen germination in Arabidopsis thaliana

Genome-wide identification, characterization and expression analysis of HAK genes and decoding their role in responding to potassium deficiency and abiotic stress in Medicago truncatula

Arabidopsis COG Complex Subunits COG3 and COG8 Modulate Golgi Morphology, Vesicle Trafficking Homeostasis and Are Essential for Pollen Tube Growth

Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis

Arabidopsis EXO70A1 recruits Patellin3 to the cell membrane independent of its role as an exocyst subunit

Hawthorn Polyphenol Extract Inhibits UVB-Induced Skin Photoaging by Regulating MMP Expression and Type I Procollagen Production in Mice

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

WeChat App in the follow up of thyroid cancer patients after thyroidectomy during the COVID‐19 pandemic

Lonicera caerulea Berry Polyphenols Activate SIRT1, Enhancing Inhibition of Raw264.7 Macrophage Foam Cell Formation and Promoting Cholesterol Efflux

Inhibition of ribosome biogenesis by actinomycin D affects Arabidopsis root development

The study of integrated care strategies to prevent low birth weight children gastrointestinal disease

Protective effects of hawthorn (Crataegus pinnatifida) polyphenol extract against UVB‐induced skin damage by modulating the p53 mitochondrial pathway in vitro and in vivo

Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model

Genetic Polymorphism of LBX1 Is Associated With Adolescent Idiopathic Scoliosis in Northern Chinese Han Population

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome

A single cohort, open-label study of the efficacy of pamidronate for palmoplantar pustulosis in synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome

TBX6 missense variants expand the mutational spectrum in a non‐Mendelian inheritance disease

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