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Extracting Forest Parameters based on Stand Automatic Segmentation Algorithm

Scientific reports, 2020-01, Vol.10 (1), p.1571-1571, Article 1571

2020

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Above-Ground Biomass Estimation of Plantation with Complex Forest Stand Structure Using Multiple Features from Airborne Laser Scanning Point Cloud Data

Forests, 2021-12, Vol.12 (12), p.1713

2021

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Above-Ground Biomass Estimation of Plantation with Different Tree Species Using Airborne LiDAR and Hyperspectral Data

Remote sensing (Basel, Switzerland), 2022-05, Vol.14 (11), p.2568

2022

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Analysis of ischemic neuronal injury in CaV2.1 channel α1 subunit mutant mice

Biochemical and biophysical research communications, 2013-04, Vol.434 (1), p.60-64

2013

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Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels

Cell research, 2011-09, Vol.21 (9), p.1343-1357

2011

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Metabolomic analysis reveals metabolic disturbance in the cortex and hippocampus of subchronic MK-801 treated rats

PloS one, 2013-04, Vol.8 (4), p.e60598-e60598

2013

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Identification of duplication downstream of BMP2 in a Chinese family with brachydactyly type A2 (BDA2)

PloS one, 2014-04, Vol.9 (4), p.e94201

2014

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NMDA Receptor Hypofunction Induces Dysfunctions of Energy Metabolism And Semaphorin Signaling in Rats: A Synaptic Proteome Study

Schizophrenia bulletin, 2012-05, Vol.38 (3), p.579-591

2012

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Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysis

Genomics (San Diego, Calif.), 2012-04, Vol.99 (4), p.220-226

2012

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Proteome alterations of cortex and hippocampus tissues in mice subjected to vitamin A depletion

The Journal of nutritional biochemistry, 2011-11, Vol.22 (11), p.1003-1008

2011

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A novel locus of coralliform cataract mapped to chromosome 2p24-pter

Journal of human genetics, 2005-06, Vol.50 (6), p.305-310

2005

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No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese population

Neuroscience letters, 2011-01, Vol.487 (1), p.61-65

2011

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Variants in TRIM44 Cause Aniridia by Impairing PAX6 Expression

Human mutation, 2015-12, Vol.36 (12), p.1164-1167

2015

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Identification of a Novel KRT9 Frameshift Mutation in a Chinese Pedigree with Epidermolytic Palmoplantar Keratoderma

International journal of human genetics, 2021-12, Vol.21 (4), p.176

Shu, Anli

2021

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Two FSHR variants, haplotypes and meta-analysis in Chinese women with premature ovarian failure and polycystic ovary syndrome

Molecular genetics and metabolism, 2010-07, Vol.100 (3), p.292-295

2010

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Study on the inhibitory effect of allicin on human gastric cancer cell line SGC-7901 and its mechanism

African journal of traditional, complementary, and alternative medicines, 2014-01, Vol.11 (1), p.176-179

2014

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Label-free quantitative proteomic analysis reveals dysfunction of complement pathway in peripheral blood of schizophrenia patients: evidence for the immune hypothesis of schizophrenia

Molecular bioSystems, 2012-01, Vol.8 (10), p.2664-2671

2012

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A Comparative Proteomics Analysis of Rat Mitochondria from the Cerebral Cortex and Hippocampus in Response to Antipsychotic Medications

Journal of proteome research, 2009-07, Vol.8 (7), p.3633-3641

2009

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Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract

BMC medical genetics, 2013-10, Vol.14 (1), p.107-107, Article 107

2013

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Association between the PDE4D gene and ischaemic stroke in the Chinese Han population

Clinical science (1979), 2009-10, Vol.117 (7), p.265

2009

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An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigree

Molecular vision, 2011-12, Vol.17, p.3200-3207

2011

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A splice site mutation in CRYBA1/A3 causing autosomal dominant posterior polar cataract in a Chinese pedigree

Molecular vision, 2010-02, Vol.16, p.154-160

2010

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The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese family

Molecular vision, 2007-10, Vol.13, p.2023-2029

2007

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Progressive sutural cataract associated with a BFSP2 mutation in a Chinese family

Molecular vision, 2006-12, Vol.12, p.1626-1631

2006

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Extracting Forest Parameters based on Stand Automatic Segmentation Algorithm

Above-Ground Biomass Estimation of Plantation with Complex Forest Stand Structure Using Multiple Features from Airborne Laser Scanning Point Cloud Data

Above-Ground Biomass Estimation of Plantation with Different Tree Species Using Airborne LiDAR and Hyperspectral Data

Analysis of ischemic neuronal injury in CaV2.1 channel α1 subunit mutant mice

Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels

Metabolomic analysis reveals metabolic disturbance in the cortex and hippocampus of subchronic MK-801 treated rats

Identification of duplication downstream of BMP2 in a Chinese family with brachydactyly type A2 (BDA2)

NMDA Receptor Hypofunction Induces Dysfunctions of Energy Metabolism And Semaphorin Signaling in Rats: A Synaptic Proteome Study

Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysis

Proteome alterations of cortex and hippocampus tissues in mice subjected to vitamin A depletion

A novel locus of coralliform cataract mapped to chromosome 2p24-pter

No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese population

Variants in TRIM44 Cause Aniridia by Impairing PAX6 Expression

Identification of a Novel KRT9 Frameshift Mutation in a Chinese Pedigree with Epidermolytic Palmoplantar Keratoderma

Two FSHR variants, haplotypes and meta-analysis in Chinese women with premature ovarian failure and polycystic ovary syndrome

Study on the inhibitory effect of allicin on human gastric cancer cell line SGC-7901 and its mechanism

Label-free quantitative proteomic analysis reveals dysfunction of complement pathway in peripheral blood of schizophrenia patients: evidence for the immune hypothesis of schizophrenia

A Comparative Proteomics Analysis of Rat Mitochondria from the Cerebral Cortex and Hippocampus in Response to Antipsychotic Medications

Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract

Association between the PDE4D gene and ischaemic stroke in the Chinese Han population

An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigree

A splice site mutation in CRYBA1/A3 causing autosomal dominant posterior polar cataract in a Chinese pedigree

The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese family

Progressive sutural cataract associated with a BFSP2 mutation in a Chinese family

Label-free quantitative proteomic analysis reveals dysfunction of complement pathway in peripheral blood of schizophrenia patients: evidence for the immune hypothesis of schizophreniaElectronic supplementary information (ESI) available. See DOI: 10.1039/c2mb25158b

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