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Cardiomyocyte-Restricted Knockout of STAT3 Results in Higher Sensitivity to Inflammation, Cardiac Fibrosis, and Heart Failure with Advanced Age

Proceedings of the National Academy of Sciences - PNAS, 2003-10, Vol.100 (22), p.12929-12934

2003

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Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population

Nature genetics, 2011-04, Vol.43 (4), p.345-349

2011

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STAT3 activation protects retinal ganglion cell layer neurons in response to stress

Experimental eye research, 2008-06, Vol.86 (6), p.991-997

2008

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STAT3 activation in response to growth factors or cytokines participates in retina precursor proliferation

Experimental eye research, 2005-07, Vol.81 (1), p.103-115

2005

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Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema

Zhonghua yi xue yi chuan xue za zhi, 2010-08, Vol.27 (4), p.371

2010

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Analysis of PAX6 gene in a Chinese family with congenital aniridia

Chung-hua yen k'o tsa chih, 2009-10, Vol.45 (10), p.931

2009

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c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor

Zhonghua yi xue yi chuan xue za zhi, 2010-06, Vol.27 (3), p.259

2010

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Two variants in MYOC and CYP1B1 genes in a Chinese family with primary angle-closure glaucoma

Zhonghua yi xue yi chuan xue za zhi, 2008-10, Vol.25 (5), p.493

2008

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Mutation of Thr704Met in SCN 4A causes normoKPP in a Chinese family

Yíchuán, 2006-08, Vol.28 (8), p.923

2006

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NF1 mutation analysis in a Chinese family with neuro- fibromatosis type

Yíchuán, 2008-03, Vol.30 (3), p.309

2008

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Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia

Chinese medical journal, 2007-06, Vol.120 (11), p.1017-1019

2007

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Advances in the studies on the molecular and genetic aspects of epilepsy

Zhōngguó yīxué kēxuéyuàn xuébào, 2005-06, Vol.27 (3), p.388

2005

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Comprehensive in silico functional specification of mouse retina transcripts

BMC genomics, 2005-03, Vol.6 (1), p.40-40, Article 40

2005

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A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33

Human genetics, 2008-11, Vol.124 (4), p.423-429

2008

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Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment

Yíchuán, 2007-02, Vol.29 (2), p.172

2007

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Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix

Zhonghua yi xue yi chuan xue za zhi, 2008-04, Vol.25 (2), p.141

2008

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A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family

Zhonghua yi xue yi chuan xue za zhi, 2008-12, Vol.25 (6), p.649

2008

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A biphasic pattern of gene expression during mouse retina development

BMC developmental biology, 2006-10, Vol.6 (1), p.48-48, Article 48

2006

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Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects

Zhonghua yi xue yi chuan xue za zhi, 2006-04, Vol.23 (2), p.134

2006

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The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family

Zhonghua yi xue yi chuan xue za zhi, 2006-10, Vol.23 (5), p.481

2006

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Genetic Analysis of a Family with 46, XY “Female” Associated with Infertility

Yíchuán xuébào, 2006, Vol.33 (1), p.19-25

2006

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Mutation p.Arg954Trp of KIF21A Causes Congenital Fibrosis of the Extraocular Muscles in a Chinese Family

Yíchuán xuébào, 2006-08, Vol.33 (8), p.685-691

2006

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Comparison of gene expression during in vivo and in vitro postnatal retina development

Journal of ocular biology, diseases, and informatics, 2008-12, Vol.1 (2-4), p.59-72

2008

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Seasonal and diurnal variations of atmospheric peroxyacetyl nitrate, peroxypropionyl nitrate, and carbon tetrachloride in Beijing

Journal of environmental sciences (China), 2014, Vol.26 (1), p.65-74

2014

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Comment on: "The platelet-to-lymphocyte ratio is a complementary prognostic factor to tumor markers in predicting early recurrence of hepatocellular carcinoma after hepatectomy"

Journal of surgical oncology, 2024-05

2024

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Cardiomyocyte-Restricted Knockout of STAT3 Results in Higher Sensitivity to Inflammation, Cardiac Fibrosis, and Heart Failure with Advanced Age

Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population

STAT3 activation protects retinal ganglion cell layer neurons in response to stress

STAT3 activation in response to growth factors or cytokines participates in retina precursor proliferation

Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema

Analysis of PAX6 gene in a Chinese family with congenital aniridia

c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor

Two variants in MYOC and CYP1B1 genes in a Chinese family with primary angle-closure glaucoma

Mutation of Thr704Met in SCN 4A causes normoKPP in a Chinese family

NF1 mutation analysis in a Chinese family with neuro- fibromatosis type

Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia

Advances in the studies on the molecular and genetic aspects of epilepsy

Comprehensive in silico functional specification of mouse retina transcripts

A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33

Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment

Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix

A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family

A biphasic pattern of gene expression during mouse retina development

Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects

The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family

Genetic Analysis of a Family with 46, XY “Female” Associated with Infertility

Mutation p.Arg954Trp of KIF21A Causes Congenital Fibrosis of the Extraocular Muscles in a Chinese Family

Comparison of gene expression during in vivo and in vitro postnatal retina development

Seasonal and diurnal variations of atmospheric peroxyacetyl nitrate, peroxypropionyl nitrate, and carbon tetrachloride in Beijing

Comment on: "The platelet-to-lymphocyte ratio is a complementary prognostic factor to tumor markers in predicting early recurrence of hepatocellular carcinoma after hepatectomy"

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