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Finite Element Analysis on the Anisotropic Characteristics of 3D Woven Resin Matrix Composites under Lateral Compression

Journal of physics. Conference series, 2023-04, Vol.2460 (1), p.12103

2023

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Design of an ultracompact optical gas sensor based on a photonic crystal nanobeam cavity

Laser physics letters, 2012-12, Vol.9 (12), p.875-878

2012

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MicroRNA-19a-3p suppresses invasion and metastasis of prostate cancer via inhibiting SOX4

European review for medical and pharmacological sciences, 2018-10, Vol.22 (19), p.6245

2018

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Family-based association study of DTNBP1 in 6p22.3 and schizophrenia

Molecular psychiatry, 2003-08, Vol.8 (8), p.717-718

2003

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A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

Clinical genetics, 2007-11, Vol.72 (5), p.471-477

2007

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Non-thermal emission from the termination of microquasar jets interacting with the interstellar medium

Monthly notices of the Royal Astronomical Society, 2011-01, Vol.410 (2), p.978-983

2011

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High-energy neutrino emission from low-mass microquasars

Monthly notices of the Royal Astronomical Society, 2010-10, Vol.407 (4), p.2468-2474

2010

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Further evidence for the association between G72 G30 genes and schizophrenia in two ethnically distinct populations

Molecular psychiatry, 2006-05, Vol.11 (5), p.479-487

2006

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Positive association between variations in CDKAL1 and type 2 diabetes in Han Chinese individuals

Diabetologia, 2008-11, Vol.51 (11), p.2134-2137

2008

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Local sampling mean discriminant analysis with kernels

Electronics letters, 2012-01, Vol.48 (1), p.22-23

2012

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Distortionless large-ratio stretcher for ultra-short pulses using photonic crystal fiber

Optics express, 2010-06, Vol.18 (12), p.12341-12347

2010

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A study of rare structural variants in schizophrenia patients and normal controls from Chinese Han population

Molecular psychiatry, 2008-10, Vol.13 (10), p.911-913

2008

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Design of A Permanent Quadrupole Magnet with Adjustable Magnetic Field Gradient

Journal of physics. Conference series, 2024-01, Vol.2687 (2), p.22029

2024

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Association of SNPs and haplotypes in GABAA receptor β2 gene with schizophrenia

Molecular psychiatry, 2004-06, Vol.9 (6), p.603-608

2004

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Polymorphisms within 5′ end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population

Molecular psychiatry, 2004-01, Vol.9 (1), p.11-12

2004

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Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

Clinical genetics, 2008-04, Vol.73 (4), p.391-394

2008

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Possible association of the MAG locus with schizophrenia in a Chinese Han cohort of family trios

Schizophrenia research, 2005-06, Vol.75 (1), p.11-19

2005

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Beam reference orbit compensation for the HLS-II storage ring

Journal of instrumentation, 2023-06, Vol.18 (6), p.T06004

2023

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Insulin-degrading enzyme and Alzheimer disease: a genetic association study in the Han Chinese

Neurology, 2004-07, Vol.63 (2), p.241-245

2004

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First Report of Botrytis cinerea Causing Gray Mold of Tobacco in Guizhou Province of China

Plant disease, 2011-05, Vol.95 (5), p.612-612

2011

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Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts

British journal of dermatology (1951), 2003-03, Vol.148 (3), p.452-455

2003

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Interleukin-10 −1082 promoter polymorphism is associated with schizophrenia in a Han Chinese sib-pair study

Neuroscience letters, 2006-02, Vol.394 (1), p.1-4

2006

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Positive association of the DIO2 (deiodinase type 2) gene with mental retardation in the iodine-deficient areas of China

Journal of medical genetics, 2004-08, Vol.41 (8), p.585-590

2004

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Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families

British journal of dermatology (1951), 2008-07, Vol.159 (1), p.238-240

2008

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Family-based association study of Epsin 4 and Schizophrenia

Molecular psychiatry, 2006-04, Vol.11 (4), p.395-399

2006

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Finite Element Analysis on the Anisotropic Characteristics of 3D Woven Resin Matrix Composites under Lateral Compression

Design of an ultracompact optical gas sensor based on a photonic crystal nanobeam cavity

MicroRNA-19a-3p suppresses invasion and metastasis of prostate cancer via inhibiting SOX4

Family-based association study of DTNBP1 in 6p22.3 and schizophrenia

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

Non-thermal emission from the termination of microquasar jets interacting with the interstellar medium

High-energy neutrino emission from low-mass microquasars

Further evidence for the association between G72 G30 genes and schizophrenia in two ethnically distinct populations

Positive association between variations in CDKAL1 and type 2 diabetes in Han Chinese individuals

Local sampling mean discriminant analysis with kernels

Distortionless large-ratio stretcher for ultra-short pulses using photonic crystal fiber

A study of rare structural variants in schizophrenia patients and normal controls from Chinese Han population

Design of A Permanent Quadrupole Magnet with Adjustable Magnetic Field Gradient

Association of SNPs and haplotypes in GABAA receptor β2 gene with schizophrenia

Polymorphisms within 5′ end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

Possible association of the MAG locus with schizophrenia in a Chinese Han cohort of family trios

Beam reference orbit compensation for the HLS-II storage ring

Insulin-degrading enzyme and Alzheimer disease: a genetic association study in the Han Chinese

First Report of Botrytis cinerea Causing Gray Mold of Tobacco in Guizhou Province of China

Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts

Interleukin-10 −1082 promoter polymorphism is associated with schizophrenia in a Han Chinese sib-pair study

Positive association of the DIO2 (deiodinase type 2) gene with mental retardation in the iodine-deficient areas of China

Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families

Family-based association study of Epsin 4 and Schizophrenia

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