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Recent progress in epigenetics of obesity

Diabetology and metabolic syndrome, 2022-11, Vol.14 (1), p.1-171, Article 171

2022

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Single-cell analysis of diverse immune phenotypes in malignant pleural effusion

Nature communications, 2021-11, Vol.12 (1), p.6690-6690, Article 6690

2021

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The mutation screening in candidate genes related to thyroid dysgenesis by targeted next‐generation sequencing panel in the Chinese congenital hypothyroidism

Clinical endocrinology (Oxford), 2022-04, Vol.96 (4), p.617-626

2022

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Microstructural and compositional evolution of SAC305/TiN composite solder under thermal stressing

Soldering & surface mount technology, 2022-04, Vol.34 (3), p.183-190

2022

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Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansion

Nature communications, 2024-04, Vol.15 (1), p.3165-3165, Article 3165

2024

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Transcriptome analysis explores genes related to shikonin biosynthesis in Lithospermeae plants and provides insights into Boraginales' evolutionary history

Scientific reports, 2017-06, Vol.7 (1), p.4477-11, Article 4477

2017

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Genetic Manipulation on Zebrafish duox Recapitulate the Clinical Manifestations of Congenital Hypothyroidism

Endocrinology (Philadelphia), 2021-08, Vol.162 (8), p.1

2021

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Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κB

Nature communications, 2023-12, Vol.14 (1), p.8082-8082, Article 8082

2023

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Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway

Journal of medical genetics, 2023-09, Vol.60 (9), p.874-884

2023

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Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis

Genetics in medicine, 2021-10, Vol.23 (10), p.1944-1951

2021

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T Cell Receptor Repertoire Analysis Reveals Signatures of T Cell Responses to Human Mycobacterium tuberculosis

Frontiers in microbiology, 2022-02, Vol.13, p.829694-829694

2022

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A Classic Near-Infrared Probe Indocyanine Green for Detecting Singlet Oxygen

International journal of molecular sciences, 2016-02, Vol.17 (2), p.219-219

2016

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Comparison of miRNAs and Their Targets in Seed Development between Two Maize Inbred Lines by High-Throughput Sequencing and Degradome Analysis

PloS one, 2016-07, Vol.11 (7), p.e0159810

2016

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TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism

Annals of Laboratory Medicine, 2024, 44(4), , pp.343-353

2024

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The isl2a transcription factor regulates pituitary development in zebrafish

Frontiers in endocrinology (Lausanne), 2023-02, Vol.14, p.920548-920548

2023

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Involvement of LeMDR, an ATP-binding cassette protein gene, in shikonin transport and biosynthesis in Lithospermum erythrorhizon

BMC plant biology, 2017-11, Vol.17 (1), p.198-198, Article 198

2017

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CCL5-Secreting Virtual Memory CD8+ T Cells Inversely Associate With Viral Reservoir Size in HIV‐1−Infected Individuals on Antiretroviral Therapy

Frontiers in immunology, 2022-05, Vol.13, p.897569-897569

2022

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Novel Compound Heterozygous Pathogenic Mutations of SLC5A5 in a Chinese Patient With Congenital Hypothyroidism

Frontiers in endocrinology (Lausanne), 2021-03, Vol.12, p.620117-620117

2021

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Heterologous overexpression of Lithospermum erythrorhizon LeERF-1 gene increases drought and pathogen resistance in Arabidopsis

Acta physiologiae plantarum, 2019-02, Vol.41 (2), Article 24

2019

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Candidate gene associations reveal sex‐specific Graves’ disease risk alleles among Chinese Han populations

Molecular genetics & genomic medicine, 2020-07, Vol.8 (7), p.e1249-n/a

2020

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Anti-IFN-γ autoantibodies underlie disseminated Talaromyces marneffei infections

The Journal of experimental medicine, 2020-12, Vol.217 (12)

2020

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Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling

Thyroid (New York, N.Y.), 2024-03, Vol.34 (3), p.324-335

2024

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Large-scale forward genetic screening of zebrafish affecting thyroid development

Biochemical and biophysical research communications, 2023-01, Vol.642, p.21-26

2023

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Molecular and clinical genetics of the transcription factor GLIS3 in Chinese congenital hypothyroidism

Molecular and cellular endocrinology, 2021-05, Vol.528, p.111223-111223, Article 111223

2021

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The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism

Molecular and cellular endocrinology, 2020-04, Vol.506, p.110761-110761, Article 110761

2020

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Recent progress in epigenetics of obesity

Single-cell analysis of diverse immune phenotypes in malignant pleural effusion

The mutation screening in candidate genes related to thyroid dysgenesis by targeted next‐generation sequencing panel in the Chinese congenital hypothyroidism

Microstructural and compositional evolution of SAC305/TiN composite solder under thermal stressing

Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansion

Transcriptome analysis explores genes related to shikonin biosynthesis in Lithospermeae plants and provides insights into Boraginales' evolutionary history

Genetic Manipulation on Zebrafish duox Recapitulate the Clinical Manifestations of Congenital Hypothyroidism

Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κB

Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway

Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis

T Cell Receptor Repertoire Analysis Reveals Signatures of T Cell Responses to Human Mycobacterium tuberculosis

A Classic Near-Infrared Probe Indocyanine Green for Detecting Singlet Oxygen

Comparison of miRNAs and Their Targets in Seed Development between Two Maize Inbred Lines by High-Throughput Sequencing and Degradome Analysis

TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism

The isl2a transcription factor regulates pituitary development in zebrafish

Involvement of LeMDR, an ATP-binding cassette protein gene, in shikonin transport and biosynthesis in Lithospermum erythrorhizon

CCL5-Secreting Virtual Memory CD8+ T Cells Inversely Associate With Viral Reservoir Size in HIV‐1−Infected Individuals on Antiretroviral Therapy

Novel Compound Heterozygous Pathogenic Mutations of SLC5A5 in a Chinese Patient With Congenital Hypothyroidism

Heterologous overexpression of Lithospermum erythrorhizon LeERF-1 gene increases drought and pathogen resistance in Arabidopsis

Candidate gene associations reveal sex‐specific Graves’ disease risk alleles among Chinese Han populations

Anti-IFN-γ autoantibodies underlie disseminated Talaromyces marneffei infections

Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling

Large-scale forward genetic screening of zebrafish affecting thyroid development

Molecular and clinical genetics of the transcription factor GLIS3 in Chinese congenital hypothyroidism

The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism

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