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Genetic Association of Pulmonary Surfactant Protein Genes, SFTPA1, SFTPA2, SFTPB, SFTPC, and SFTPD With Cystic Fibrosis

Frontiers in immunology, 2018-10, Vol.9, p.2256-2256

2018

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High-throughput DNA methylation profiling using universal bead arrays

Genome Research, 2006-03, Vol.16 (3), p.383-393

2006

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Sex and SP-A2 Dependent NAD(H) Redox Alterations in Mouse Alveolar Macrophages in Response to Ozone Exposure: Potential Implications for COVID-19

Antioxidants, 2020-09, Vol.9 (10), p.915

2020

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Mutations in IRGM Are Associated With More Frequent Need for Surgery in Patients With Ileocolonic Crohnʼs Disease

Diseases of the colon & rectum, 2012-02, Vol.55 (2), p.115-121

2012

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Association of the haem oxygenase-1 gene with inflammatory bowel disease

Swiss medical weekly, 2017-08, Vol.147 (3132), p.w14456

2017

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Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis

Human genetics, 2003-11, Vol.113 (6), p.542-550

2003

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NKX2-3 transcriptional regulation of endothelin-1 and VEGF signaling in human intestinal microvascular endothelial cells

PloS one, 2011-05, Vol.6 (5), p.e20454-e20454

2011

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Genes Regulated by Nkx2-3 in Sporadic and Inflammatory Bowel Disease-Associated Colorectal Cancer Cell Lines

Digestive diseases and sciences, 2010-11, Vol.55 (11), p.3171-3180

2010

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Surfactant protein A, an innate immune factor, is expressed in the vaginal mucosa and is present in vaginal lavage fluid

Immunology, 2004-01, Vol.111 (1), p.91-99

2004

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Single nucleotide polymorphisms (SNPs) of TNFSF15 are associated with surgical diverticulitis

Journal of the American College of Surgeons, 2012-09, Vol.215 (3), p.S32-S32

2012

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Genes regulated by Nkx2-3 in siRNA-mediated knockdown B cells: Implication of endothelin-1 in inflammatory bowel disease

Molecular genetics and metabolism, 2010-05, Vol.100 (1), p.88-95

2010

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DNA methylation markers of surfactant proteins in lung cancer

International journal of oncology, 2007-07, Vol.31 (1), p.181-191

2007

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Optical Redox Imaging of Lonidamine Treatment Response of Melanoma Cells and Xenografts

Molecular imaging and biology, 2019-06, Vol.21 (3), p.426-435

2019

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An SP-B Gene Mutation Responsible for SP-B Deficiency in Fatal Congenital Alveolar Proteinosis: Evidence for a Mutation Hotspot in Exon 4

Molecular genetics and metabolism, 1998-05, Vol.64 (1), p.25-35

1998

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Differential Expression of PGC1α in Intratumor Redox Subpopulations of Breast Cancer

Advances in experimental medicine and biology, 2018, Vol.1072, p.177-181

2018

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Regulation of translation by upstream translation initiation codons of surfactant protein A1 splice variants

American journal of physiology. Lung cellular and molecular physiology, 2015-01, Vol.308 (1), p.L58-L75

2015

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Identification of Disease-Associated DNA Methylation in B Cells from Crohn’s Disease and Ulcerative Colitis Patients

Digestive diseases and sciences, 2012-12, Vol.57 (12), p.3145-3153

2012

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NKX2-3 (NK2 homeobox 3)

Atlas of genetics and cytogenetics in oncology and haematology, 2017-08 (Begum Akman)

2017

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Focal Congenital Alveolar Proteinosis Associated With Abnormal Surfactant Protein B Messenger RNA

Chest, 2001-02, Vol.119 (2), p.645-647

2001

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Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient and relevance to the PSTPIP1 gene

Inflammatory bowel diseases, 2011-06, Vol.17 (6), p.E41-E42

2011

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A model for family-based case-control studies of genetic imprinting and epistasis

Briefings in bioinformatics, 2014-11, Vol.15 (6), p.1069-1079

2014

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NKX2-3 regulates MAdCAM1 and VCAM1 expression in human intestinal microvascular endothelial cells: O-17

Inflammatory bowel diseases, 2011-12, Vol.17, p.S8

2011

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NOD2 Mutations Affect Muramyl Dipeptide Stimulation of Human B Lymphocytes and Interact with Other IBD-Associated Genes

Digestive diseases and sciences, 2013-09, Vol.58 (9), p.2599-2607

2013

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Disease-associated DNA methylationin Inflammatory Bowel Disease subtypes Crohnʼs disease and Ulcerative Colitis: P-223

Inflammatory bowel diseases, 2011-12, Vol.17, p.S78

2011

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531 Mutation in ZO-1 is Associated With Protection From Familial Inflammatory Bowel Disease

Gastroenterology (New York, N.Y. 1943), 2012-05, Vol.142 (5), p.S-1029-S-1029

2012

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Genetic Association of Pulmonary Surfactant Protein Genes, SFTPA1, SFTPA2, SFTPB, SFTPC, and SFTPD With Cystic Fibrosis

High-throughput DNA methylation profiling using universal bead arrays

Sex and SP-A2 Dependent NAD(H) Redox Alterations in Mouse Alveolar Macrophages in Response to Ozone Exposure: Potential Implications for COVID-19

Mutations in IRGM Are Associated With More Frequent Need for Surgery in Patients With Ileocolonic Crohnʼs Disease

Association of the haem oxygenase-1 gene with inflammatory bowel disease

Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis

NKX2-3 transcriptional regulation of endothelin-1 and VEGF signaling in human intestinal microvascular endothelial cells

Genes Regulated by Nkx2-3 in Sporadic and Inflammatory Bowel Disease-Associated Colorectal Cancer Cell Lines

Surfactant protein A, an innate immune factor, is expressed in the vaginal mucosa and is present in vaginal lavage fluid

Single nucleotide polymorphisms (SNPs) of TNFSF15 are associated with surgical diverticulitis

Genes regulated by Nkx2-3 in siRNA-mediated knockdown B cells: Implication of endothelin-1 in inflammatory bowel disease

DNA methylation markers of surfactant proteins in lung cancer

Optical Redox Imaging of Lonidamine Treatment Response of Melanoma Cells and Xenografts

An SP-B Gene Mutation Responsible for SP-B Deficiency in Fatal Congenital Alveolar Proteinosis: Evidence for a Mutation Hotspot in Exon 4

Differential Expression of PGC1α in Intratumor Redox Subpopulations of Breast Cancer

Regulation of translation by upstream translation initiation codons of surfactant protein A1 splice variants

Identification of Disease-Associated DNA Methylation in B Cells from Crohn’s Disease and Ulcerative Colitis Patients

NKX2-3 (NK2 homeobox 3)

Focal Congenital Alveolar Proteinosis Associated With Abnormal Surfactant Protein B Messenger RNA

Failure of anakinra treatment of pyoderma gangrenosum in an IBD patient and relevance to the PSTPIP1 gene

A model for family-based case-control studies of genetic imprinting and epistasis

NKX2-3 regulates MAdCAM1 and VCAM1 expression in human intestinal microvascular endothelial cells: O-17

NOD2 Mutations Affect Muramyl Dipeptide Stimulation of Human B Lymphocytes and Interact with Other IBD-Associated Genes

Disease-associated DNA methylationin Inflammatory Bowel Disease subtypes Crohnʼs disease and Ulcerative Colitis: P-223

531 Mutation in ZO-1 is Associated With Protection From Familial Inflammatory Bowel Disease

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