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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

2018

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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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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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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 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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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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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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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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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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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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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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Genes Differentially Regulated by NKX2-3 in B Cells Between Ulcerative Colitis and Crohn’s Disease Patients and Possible Involvement of EGR1

Inflammation, 2012-06, Vol.35 (3), p.889-899

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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OCTN1 variant L503F is associated with familial and sporadic inflammatory bowel disease

Journal of Crohn's and colitis, 2010-06, Vol.4 (2), p.132-138

2010

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DLG5 P1371Q is associated with inflammatory bowel disease and complementary to R30Q in disease susceptibility

Swiss medical weekly, 2011, Vol.141, p.w13290

2011

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Murine trophoblast organoids as a model for trophoblast development and CRISPR-Cas9 screening

Developmental cell, 2023-12, Vol.58 (24), p.2992-3008.e7

2023

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Calgary score and modified Calgary score in the differential diagnosis between neurally mediated syncope and epilepsy in children

Neurological sciences, 2017-01, Vol.38 (1), p.143-149

2017

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Transient aphasia: a rare complication of head-up tilt test

Neurological sciences, 2014-07, Vol.35 (7), p.1127-1132

2014

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

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

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 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

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

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

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

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

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

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

Genes Differentially Regulated by NKX2-3 in B Cells Between Ulcerative Colitis and Crohn’s Disease Patients and Possible Involvement of EGR1

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

OCTN1 variant L503F is associated with familial and sporadic inflammatory bowel disease

DLG5 P1371Q is associated with inflammatory bowel disease and complementary to R30Q in disease susceptibility

Murine trophoblast organoids as a model for trophoblast development and CRISPR-Cas9 screening

Calgary score and modified Calgary score in the differential diagnosis between neurally mediated syncope and epilepsy in children

Transient aphasia: a rare complication of head-up tilt test

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