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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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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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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 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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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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Genetic association and epistatic interaction of the interleukin-10 signaling pathway in pediatric inflammatory bowel disease

World journal of gastroenterology : WJG, 2017-07, Vol.23 (27), p.4897-4909

2017

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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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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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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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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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NKX2-3 variant rs11190140 is associated with IBD and alters binding of NFAT

Molecular genetics and metabolism, 2011-09, Vol.104 (1-2), p.174-179

2011

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PTPN2 is Associated With Crohn's Disease (CD) and Its Up-Regulation in CD Patients Mediated by Nkx2-3

Gastroenterology (New York, N.Y. 1943), 2011, Vol.140 (5), p.S-485-S-486

2011

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PTPN2 is associated with Crohn's disease and its expression is regulated by NKX2-3

Disease markers, 2012-01, Vol.32 (2), p.83-91

2012

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PTPN2 is associated with Crohn's disease and its expression is regulated by NKX2-3

Disease markers, 2012, Vol.32 (2), p.83-91

2012

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Heterogeneous allele expression of pulmonary SP-D gene in rat large intestine and other tissues

Physiological genomics, 2002-12, Vol.11 (3), p.235-243

2002

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W1236 NOD2 Mutations Compromise Host Defense Mechanisms to Enteric Bacteria as Shown by Decreased NF-kB in Human B Cells After Muramyl Dipeptide (MDP) Stimulation

Gastroenterology (New York, N.Y. 1943), 2010, Vol.138 (5), p.S-680-S-680

2010

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W1247 Nkx2-3 Variant Rs11190140 is Associated With IBD and Alters NFAT Transcription Factor Binding

Gastroenterology (New York, N.Y. 1943), 2010, Vol.138 (5), p.S-683-S-683

2010

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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

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

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 siRNA-mediated knockdown B cells: Implication of endothelin-1 in inflammatory bowel disease

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

Genetic association and epistatic interaction of the interleukin-10 signaling pathway in pediatric inflammatory bowel disease

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

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

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

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

NKX2-3 variant rs11190140 is associated with IBD and alters binding of NFAT

PTPN2 is Associated With Crohn's Disease (CD) and Its Up-Regulation in CD Patients Mediated by Nkx2-3

PTPN2 is associated with Crohn's disease and its expression is regulated by NKX2-3

PTPN2 is associated with Crohn's disease and its expression is regulated by NKX2-3

Heterogeneous allele expression of pulmonary SP-D gene in rat large intestine and other tissues

W1236 NOD2 Mutations Compromise Host Defense Mechanisms to Enteric Bacteria as Shown by Decreased NF-kB in Human B Cells After Muramyl Dipeptide (MDP) Stimulation

W1247 Nkx2-3 Variant Rs11190140 is Associated With IBD and Alters NFAT Transcription Factor Binding

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