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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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NOD2/CARD15 Mutations Correlate With Severe Pouchitis After Ileal Pouch-Anal Anastomosis

Diseases of the colon & rectum, 2010-11, Vol.53 (11), p.1487-1494

2010

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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, p.w14456

2017

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Genetic Risk Profiling and Gene Signature Modeling to Predict Risk of Complications After IPAA

Diseases of the colon & rectum, 2012-03, Vol.55 (3), p.239-248

2012

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IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

Pediatric research, 2012-01, Vol.71 (1), p.107-114

2012

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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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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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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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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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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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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

NOD2/CARD15 Mutations Correlate With Severe Pouchitis After Ileal Pouch-Anal Anastomosis

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

Genetic Risk Profiling and Gene Signature Modeling to Predict Risk of Complications After IPAA

IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

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

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

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

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

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

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