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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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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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A general model for multilocus epistatic interactions in case-control studies

PloS one, 2010-08, Vol.5 (8), p.e11384-e11384

2010

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

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

2017

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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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Genetic Association of Nonsynonymous Variants of the IL23R with Familial and Sporadic Inflammatory Bowel Disease in Women

Digestive diseases and sciences, 2010-03, Vol.55 (3), p.739-746

2010

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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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Novel, non-radioactive, simple and multiplex PCR-cRFLP methods for genotyping human SP-A and SP-D marker alleles

Disease markers, 1999, Vol.15 (4), p.269-281

1999

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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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Protocol for Genomic DNA Preparation from Fresh or Frozen Serum for PCR Amplification

BioTechniques, 2000-09, Vol.29 (3), p.460-466

2000

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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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Genomic DNA Extraction from Small Amounts of Sera to be Used for Genotype Analysis

BioTechniques, 1998-06, Vol.24 (6), p.937-940

1998

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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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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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Multiplex Genotype Analysis of Invasive Carcinoma and Accompanying Proliferative Lesions Microdissected from Breast Tissue

The Journal of molecular diagnostics : JMD, 2000-02, Vol.2 (1), p.29-36

2000

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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

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

A general model for multilocus epistatic interactions in case-control studies

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

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

Genetic Association of Nonsynonymous Variants of the IL23R with Familial and Sporadic Inflammatory Bowel Disease in Women

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

Novel, non-radioactive, simple and multiplex PCR-cRFLP methods for genotyping human SP-A and SP-D marker alleles

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

Protocol for Genomic DNA Preparation from Fresh or Frozen Serum for PCR Amplification

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

Genomic DNA Extraction from Small Amounts of Sera to be Used for Genotype Analysis

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

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

Multiplex Genotype Analysis of Invasive Carcinoma and Accompanying Proliferative Lesions Microdissected from Breast Tissue

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

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