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Embryonic development of the ganglion plexuses and the concentric layer structure of human gut: a topographical study

Anatomy and Embryology, 2004-04, Vol.208 (1), p.33

2004

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Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-β-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations

Cell death and differentiation, 2014-06, Vol.21 (6), p.978-989

2014

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Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations

Cell death and differentiation, 2014-06, Vol.21 (6), p.990-997

2014

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Perturbation of Hoxb5 signaling in vagal and trunk neural crest cells causes apoptosis and neurocristopathies in mice

Cell death and differentiation, 2014-02, Vol.21 (2), p.278-289

2014

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Depletion of intestinal resident macrophages prevents ischaemia reperfusion injury in gut

Gut, 2004-12, Vol.53 (12), p.1772-1780

2004

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Association study of PHOX2B as a candidate gene for Hirschsprung’s disease

Gut, 2003-04, Vol.52 (4), p.563-567

2003

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Deficient motor innervation of the sphincter mechanism in fetal rats with anorectal malformation: a quantitative study by fluorogold retrograde tracing

Journal of Pediatric Surgery, 2003-09, Vol.38 (9), p.1383-1388

2003

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Correlation Between Genetic Variations in Hox Clusters and Hirschsprung's Disease

Annals of human genetics, 2007-07, Vol.71 (4), p.526-536

2007

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SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants

Gut, 2001-08, Vol.49 (2), p.220-226

2001

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Is there a role for the IHH gene in Hirschsprung's disease?

Neurogastroenterology and motility, 2003-12, Vol.15 (6), p.663-668

2003

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Disruption of the temporally regulated cloaca endodermal [beta]-catenin signaling causes anorectal malformations

Cell death and differentiation, 2014-06, Vol.21 (6), p.990

2014

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Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-[beta]-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations

Cell death and differentiation, 2014-06, Vol.21 (6), p.978

2014

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Chinese patients with sporadic Hirschsprung’s disease are predominantly represented by a single RET haplotype

Journal of medical genetics, 2003-11, Vol.40 (11), p.e122-122

2003

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Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Human molecular genetics, 2011-03, Vol.20 (5), p.1048-1048

2011

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Role of RET and ko=PHOX2B gene polymorphisms in risk of Hirschsprung’s disease in Chinese population

Gut, 2007-05, Vol.56 (5), p.736-736

2007

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Esophageal atresia and achalasialike esophageal dysmotility

Journal of pediatric surgery, 2004-10, Vol.39 (10), p.1581-1583

2004

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Enteric nervous system, interstitial cells of cajal, and smooth muscle vacuolization in segmental dilatation of jejunum

Journal of pediatric surgery, 2001-06, Vol.36 (6), p.930-935

2001

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The mRNAs for the three chains of human collagen type XI are widely distributed but not necessarily co-expressed: implications for homotrimeric, heterotrimeric and heterotypic collagen molecules

Biochemical journal, 1995-10, Vol.311 ( Pt 2) (2), p.511-516

1995

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The human α2(XI) collagen (COL11A2) chain: molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization

The Journal of biological chemistry, 1989, Vol.264 (23), p.13910-13916

1989

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The Human α2(XI) Collagen Gene (COL11A2): Completion of Coding Information, Identification of the Promoter Sequence, and Precise Localization within the Major Histocompatibility Complex Reveal Overlap with the KE5 Gene

Genomics (San Diego, Calif.), 1996-03, Vol.32 (3), p.401-412

1996

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An EcoRI RFLP in the human α2 (XI) (COL 11A2) gene

Nucleic acids research, 1990-01, Vol.18 (2), p.387-387

1990

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Potential role of fibroblast growth factor 21 in the deterioration of bone quality in impaired glucose tolerance

Journal of endocrinological investigation, 2021-03, Vol.44 (3), p.523-530

2021

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Trion-induced negative photoconductivity in monolayer MoS2

Physical review letters, 2014-10, Vol.113 (16), p.166801-166801

2014

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Spin-induced optical conductivity in the spin-liquid candidate herbertsmithite

Physical review letters, 2013-09, Vol.111 (12), p.127401-127401, Article 127401

2013

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Photoluminescence and Electron Paramagnetic Resonance of ZnO Tetrapod Structures

Advanced functional materials, 2004-09, Vol.14 (9), p.856-864

2004

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Embryonic development of the ganglion plexuses and the concentric layer structure of human gut: a topographical study

Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-β-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations

Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations

Perturbation of Hoxb5 signaling in vagal and trunk neural crest cells causes apoptosis and neurocristopathies in mice

Depletion of intestinal resident macrophages prevents ischaemia reperfusion injury in gut

Association study of PHOX2B as a candidate gene for Hirschsprung’s disease

Deficient motor innervation of the sphincter mechanism in fetal rats with anorectal malformation: a quantitative study by fluorogold retrograde tracing

Correlation Between Genetic Variations in Hox Clusters and Hirschsprung's Disease

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants

Is there a role for the IHH gene in Hirschsprung's disease?

Disruption of the temporally regulated cloaca endodermal [beta]-catenin signaling causes anorectal malformations

Dysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-[beta]-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations

Chinese patients with sporadic Hirschsprung’s disease are predominantly represented by a single RET haplotype

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Role of RET and ko=PHOX2B gene polymorphisms in risk of Hirschsprung’s disease in Chinese population

Esophageal atresia and achalasialike esophageal dysmotility

Enteric nervous system, interstitial cells of cajal, and smooth muscle vacuolization in segmental dilatation of jejunum

The mRNAs for the three chains of human collagen type XI are widely distributed but not necessarily co-expressed: implications for homotrimeric, heterotrimeric and heterotypic collagen molecules

The human α2(XI) collagen (COL11A2) chain: molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization

The Human α2(XI) Collagen Gene (COL11A2): Completion of Coding Information, Identification of the Promoter Sequence, and Precise Localization within the Major Histocompatibility Complex Reveal Overlap with the KE5 Gene

An EcoRI RFLP in the human α2 (XI) (COL 11A2) gene

Potential role of fibroblast growth factor 21 in the deterioration of bone quality in impaired glucose tolerance

Trion-induced negative photoconductivity in monolayer MoS2

Spin-induced optical conductivity in the spin-liquid candidate herbertsmithite

Photoluminescence and Electron Paramagnetic Resonance of ZnO Tetrapod Structures

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