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The effects of land subsidence and rehabilitation on soil hydraulic properties in a mining area in the Loess Plateau of China

Catena (Giessen), 2017-12, Vol.159, p.51-59

2017

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Circulating MicroRNAs in Cancer: Potential and Challenge

Frontiers in genetics, 2019-07, Vol.10, p.626-626

2019

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Construction and application of adenoviral vectors

Molecular therapy. Nucleic acids, 2023-12, Vol.34, p.102027-102027, Article 102027

2023

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Arabidopsis ADF1 is Regulated by MYB73 and is Involved in Response to Salt Stress Affecting Actin Filament Organization

Plant and cell physiology, 2021-11, Vol.62 (9), p.1387-1395

2021

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Joint application of A-InDels and miniSTRs for forensic personal, full and half sibling identifications, and genetic differentiation analyses in two populations from China

BMC genomics, 2024-04, Vol.25 (1), p.329-329, Article 329

2024

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Genetic Analysis of a Case of Sotos Syndrome with Suspected Germinal Mosaicism in Mother

Applied biochemistry and biotechnology, 2023-10, Vol.195 (10), p.5792-5801

2023

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Mechanism Research of Platelet Core Marker Prediction and Molecular Recognition in Cardiovascular Events

Combinatorial chemistry & high throughput screening, 2023, Vol.26 (1), p.103

2023

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Urea Electrooxidation in Alkaline Environment: Fundamentals and Applications

ChemElectroChem, 2023-07, Vol.10 (13), p.n/a

2023

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Pseudo-capacitive and kinetic enhancement of metal oxides and pillared graphite composite for stabilizing battery anodes

Scientific reports, 2022-07, Vol.12 (1), p.12079-13, Article 12079

2022

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An intelligent music genre analysis using feature extraction and classification using deep learning techniques

Computers & electrical engineering, 2022-05, Vol.100, p.107978, Article 107978

2022

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Coupling photocatalytic CO2 reduction and CH3OH oxidation for selective dimethoxymethane production

Nature communications, 2024-07, Vol.15 (1), p.6047-15, Article 6047

2024

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Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis

Orphanet journal of rare diseases, 2023-05, Vol.18 (1), p.107-107, Article 107

2023

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Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome

Frontiers in genetics, 2023-09, Vol.14, p.1252873-1252873

2023

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Genetic Background of Kirgiz Ethnic Group From Northwest China Revealed by Mitochondrial DNA Control Region Sequences on Massively Parallel Sequencing

Frontiers in genetics, 2022-02, Vol.13, p.729514-729514

2022

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Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Zhonghua yi xue yi chuan xue za zhi, 2023-08, Vol.40 (8), p.966

2023

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Urea Electrooxidation in Alkaline Environment: Fundamentals and Applications

ChemElectroChem, 2023-07, Vol.10 (13), p.n/a

2023

Volltextzugriff (PDF)

Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

Zhonghua yi xue yi chuan xue za zhi, 2023-02, Vol.40 (2), p.230

2023

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Study on the degradation and metabolic mechanism of four quinolone antibiotics by mixed strains

Frontiers in environmental chemistry, 2024-02, Vol.5

2024

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Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome

Clinica chimica acta, 2017-10, Vol.473, p.26-31

2017

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Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

Open life sciences, 2023-05, Vol.18 (1), p.20220593-20220593

2023

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METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA

Frontiers in cell and developmental biology, 2022-06, Vol.10, p.894810-894810

2022

Volltextzugriff (PDF)

Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Zhonghua yi xue yi chuan xue za zhi, 2021-01, Vol.38 (1), p.52

2021

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Genetic analysis of 90 families affected with spinal muscular atrophy

Zhonghua yi xue yi chuan xue za zhi, 2020-02, Vol.37 (2), p.116

2020

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Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Zhonghua yi xue yi chuan xue za zhi, 2020-01, Vol.37 (1), p.17

2020

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A novel MIP mutation in familial congenital nuclear cataracts

European journal of medical genetics, 2016-09, Vol.59 (9), p.488-491

2016

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The effects of land subsidence and rehabilitation on soil hydraulic properties in a mining area in the Loess Plateau of China

Circulating MicroRNAs in Cancer: Potential and Challenge

Construction and application of adenoviral vectors

Arabidopsis ADF1 is Regulated by MYB73 and is Involved in Response to Salt Stress Affecting Actin Filament Organization

Joint application of A-InDels and miniSTRs for forensic personal, full and half sibling identifications, and genetic differentiation analyses in two populations from China

Genetic Analysis of a Case of Sotos Syndrome with Suspected Germinal Mosaicism in Mother

Mechanism Research of Platelet Core Marker Prediction and Molecular Recognition in Cardiovascular Events

Urea Electrooxidation in Alkaline Environment: Fundamentals and Applications

Pseudo-capacitive and kinetic enhancement of metal oxides and pillared graphite composite for stabilizing battery anodes

An intelligent music genre analysis using feature extraction and classification using deep learning techniques

Coupling photocatalytic CO2 reduction and CH3OH oxidation for selective dimethoxymethane production

Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis

Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome

Genetic Background of Kirgiz Ethnic Group From Northwest China Revealed by Mitochondrial DNA Control Region Sequences on Massively Parallel Sequencing

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Urea Electrooxidation in Alkaline Environment: Fundamentals and Applications

Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

Study on the degradation and metabolic mechanism of four quinolone antibiotics by mixed strains

Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing

METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA

Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Genetic analysis of 90 families affected with spinal muscular atrophy

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

A novel MIP mutation in familial congenital nuclear cataracts

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