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SnS2 Nanosheets Coating on Nanohollow Cubic CoS2/C for Ultralong Life and High Rate Capability Half/Full Sodium‐Ion Batteries

Small (Weinheim an der Bergstrasse, Germany), 2018-10, Vol.14 (41), p.e1802716-n/a

2018

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Metabolism and antioxidant activity of SlGSTD1 in Spodoptera litura as a detoxification enzyme to pyrethroids

Scientific reports, 2022-06, Vol.12 (1), p.10108-10108, Article 10108

2022

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Biological response of earthworm, Eisenia fetida, to five neonicotinoid insecticides

Chemosphere (Oxford), 2015-08, Vol.132, p.120-126

2015

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Characterization of resistance and fitness cost of Descurainia sophia L. populations from Henan and Xinjiang, China

Scientific reports, 2021-07, Vol.11 (1), p.14655-14655, Article 14655

2021

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The low-lethal concentrations of rotenone and pyrethrins suppress the population growth of Rhopalosiphum padi

Scientific reports, 2024-07, Vol.14 (1), p.16570-11, Article 16570

2024

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A Lipopolysaccharide O-Antigen Synthesis Gene in Mesorhizobium huakuii Plays Differentiated Roles in Root Nodule Symbiotic Compatibility with Astragalus sinicus

Molecular plant-microbe interactions, 2023-10, Vol.36 (10), p.623-635

2023

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Analysis of Outer Membrane Vesicles Indicates That Glycerophospholipid Metabolism Contributes to Early Symbiosis Between Sinorhizobium fredii HH103 and Soybean

Molecular plant-microbe interactions, 2022-04, Vol.35 (4), p.311-322

2022

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Preparedness of Our Emergency Department During the Coronavirus Disease Outbreak from the Nurses’ Perspectives: A Qualitative Research Study

Journal of emergency nursing, 2020-11, Vol.46 (6), p.848-861.e1

2020

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Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature

Frontiers in genetics, 2024-08, Vol.15, p.1448341

2024

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Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

Genome medicine, 2022-10, Vol.14 (1), p.1-123, Article 123

2022

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Exploration and Practice of High-Quality Talent Cultivation Path in the Context of Industry-Education Integration Drive

Applied mathematics and nonlinear sciences, 2024-01, Vol.9 (1)

2024

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Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center

Prenatal diagnosis, 2021-05, Vol.41 (6), p.690-696

2021

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Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing

Frontiers in genetics, 2023, Vol.14, p.1260995-1260995

2023

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Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants

Frontiers in genetics, 2023-12, Vol.14, p.1254265-1254265

2023

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Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China

BMC medical genetics, 2020-02, Vol.21 (1), p.43-43, Article 43

2020

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Case Report: Early diagnosis of lethal multiple pterygium syndrome with micrognathia: Two novel mutations in the CHRND gene

Frontiers in genetics, 2023-01, Vol.14, p.1005624

2023

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Genetic diagnosis of fetal microcephaly at a single tertiary center in China

Frontiers in genetics, 2023-05, Vol.14, p.1112153-1112153

2023

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Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma

BMC medical genomics, 2024-04, Vol.17 (1), p.96-96, Article 96

2024

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Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center

Italian journal of pediatrics, 2024-08, Vol.50 (1), p.152-9

2024

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Exome sequencing improves genetic diagnosis of congenital orofacial clefts

Frontiers in genetics, 2023-09, Vol.14, p.1252823-1252823

2023

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Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants

Frontiers in genetics, 2023-07, Vol.14, p.1208102-1208102

2023

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PDIA2 variant associated with vitiligo

Skin health and disease, 2023-10, Vol.3 (5), p.e278-e278

2023

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The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study

Frontiers in genetics, 2022-04, Vol.13, p.856522-856522

2022

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Prenatal diagnosis and perinatal outcomes of twin pregnancies disharmonious for one fetus with nuchal translucency above the 95th percentile

Molecular cytogenetics, 2023-11, Vol.16 (1), p.1-30, Article 30

2023

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Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

Frontiers in genetics, 2022-09, Vol.13, p.951829-951829

2022

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SnS2 Nanosheets Coating on Nanohollow Cubic CoS2/C for Ultralong Life and High Rate Capability Half/Full Sodium‐Ion Batteries

Metabolism and antioxidant activity of SlGSTD1 in Spodoptera litura as a detoxification enzyme to pyrethroids

Biological response of earthworm, Eisenia fetida, to five neonicotinoid insecticides

Characterization of resistance and fitness cost of Descurainia sophia L. populations from Henan and Xinjiang, China

The low-lethal concentrations of rotenone and pyrethrins suppress the population growth of Rhopalosiphum padi

A Lipopolysaccharide O-Antigen Synthesis Gene in Mesorhizobium huakuii Plays Differentiated Roles in Root Nodule Symbiotic Compatibility with Astragalus sinicus

Analysis of Outer Membrane Vesicles Indicates That Glycerophospholipid Metabolism Contributes to Early Symbiosis Between Sinorhizobium fredii HH103 and Soybean

Preparedness of Our Emergency Department During the Coronavirus Disease Outbreak from the Nurses’ Perspectives: A Qualitative Research Study

Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature

Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

Exploration and Practice of High-Quality Talent Cultivation Path in the Context of Industry-Education Integration Drive

Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center

Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing

Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants

Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China

Case Report: Early diagnosis of lethal multiple pterygium syndrome with micrognathia: Two novel mutations in the CHRND gene

Genetic diagnosis of fetal microcephaly at a single tertiary center in China

Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center

Exome sequencing improves genetic diagnosis of congenital orofacial clefts

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants

PDIA2 variant associated with vitiligo

The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study

Prenatal diagnosis and perinatal outcomes of twin pregnancies disharmonious for one fetus with nuchal translucency above the 95th percentile

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

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