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Trefoil factors in inflammatory bowel disease

World journal of gastroenterology : WJG, 2014-03, Vol.20 (12), p.3223-3230

2014

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DNA Methylation Signatures for Prediction of Biochemical Recurrence After Radical Prostatectomy of Clinically Localized Prostate Cancer

Journal of clinical oncology, 2013-09, Vol.31 (26), p.3250-3258

2013

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17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2934-2942

2016

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Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women

Prenatal diagnosis, 2016-12, Vol.36 (12), p.1127-1134

2016

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Absolute immature platelet count may predict imminent platelet recovery in thrombocytopenic children following chemotherapy

Pediatric blood & cancer, 2013-07, Vol.60 (7), p.1198-1203

2013

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Comprehensive Evaluation of TFF3 Promoter Hypomethylation and Molecular Biomarker Potential for Prostate Cancer Diagnosis and Prognosis

International journal of molecular sciences, 2017-09, Vol.18 (9), p.2017

2017

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Transposition of the great arteries-a phenotype associated with 16p11.2 duplications?

World journal of cardiology, 2017-12, Vol.9 (12), p.848-852

2017

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Plasma Levels of Trefoil Factors are Increased in Patients with Advanced Prostate Cancer

Clinical cancer research, 2006-02, Vol.12 (3), p.807-812

2006

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Clinical aspects of altered glycosylation of glycoproteins in cancer

Electrophoresis, 1999-02, Vol.20 (2), p.362-371

1999

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Clinical value of smear review of flagged samples analyzed with the Sysmex XN hematology analyzer

Clinical chemistry and laboratory medicine, 2024-09

2024

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Diagnostic performance of the CellaVision preclassification neutrophil count - time to bypass the reclassification?

Scandinavian journal of clinical and laboratory investigation, 2024-07, Vol.84 (4), p.278-284

2024

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Development and Evaluation of an ELISA for Human Trefoil Factor 3

Clinical chemistry (Baltimore, Md.), 2002-10, Vol.48 (10), p.1689-1695

2002

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Use of cell‐free non‐invasive prenatal testing in pregnancies affected by placental mosaicism

Prenatal diagnosis, 2024-05, Vol.44 (5), p.562-571

2024

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Infant Ustekinumab Clearance, Risk of Infection, and Development After Exposure During Pregnancy

Clinical gastroenterology and hepatology, 2024-01

2024

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On the road to replacing invasive testing with cell‐based NIPT: Five clinical cases with aneuploidies, microduplication, unbalanced structural rearrangement, or mosaicism

Prenatal diagnosis, 2017-11, Vol.37 (11), p.1120-1124

2017

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A decade of change – lessons learned from prenatal diagnostics in Central Denmark region in 2008–2018

Acta obstetricia et gynecologica Scandinavica, 2023-11, Vol.102 (11), p.1505-1510

2023

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Fetal Heart Defects and Measures of Cerebral Size

The Journal of pediatrics, 2019-07, Vol.210, p.146-153

2019

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Aggressive medullary thyroid carcinoma in a ten-year-old patient with multiple endocrine neoplasia 2B due to the A883F mutation

Thyroid (New York, N.Y.), 2015-01, Vol.25 (1), p.139-140

2015

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Influence of Lewis α1-3/4-L-Fucosyltransferase (FUT3) Gene Mutations on Enzyme Activity, Erythrocyte Phenotyping, and Circulating Tumor Marker Sialyl-Lewis a Levels

The Journal of biological chemistry, 1996-12, Vol.271 (50), p.32260-32268

1996

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Placental mosaicism in the era of chromosomal microarrays

European journal of medical genetics, 2020-04, Vol.63 (4), p.103778-103778, Article 103778

2020

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Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture

American journal of human genetics, 2008-01, Vol.82 (1), p.57-72

2008

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Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings

Acta obstetricia et gynecologica Scandinavica, 2013-07, Vol.92 (7), p.762-768

2013

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National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017

Acta obstetricia et gynecologica Scandinavica, 2021-05, Vol.100 (5), p.884-892

2021

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Prenatal diagnosis of Nager syndrome in a 12-week-old fetus with a whole gene deletion of SF3B4 by chromosomal microarray

European journal of medical genetics, 2016-01, Vol.59 (1), p.48-51

2016

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Promoter hypomethylation and upregulation of trefoil factors in prostate cancer

International journal of cancer, 2010-10, Vol.127 (8), p.1857-1865

2010

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Trefoil factors in inflammatory bowel disease

DNA Methylation Signatures for Prediction of Biochemical Recurrence After Radical Prostatectomy of Clinically Localized Prostate Cancer

17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature

Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women

Absolute immature platelet count may predict imminent platelet recovery in thrombocytopenic children following chemotherapy

Comprehensive Evaluation of TFF3 Promoter Hypomethylation and Molecular Biomarker Potential for Prostate Cancer Diagnosis and Prognosis

Transposition of the great arteries-a phenotype associated with 16p11.2 duplications?

Plasma Levels of Trefoil Factors are Increased in Patients with Advanced Prostate Cancer

Clinical aspects of altered glycosylation of glycoproteins in cancer

Clinical value of smear review of flagged samples analyzed with the Sysmex XN hematology analyzer

Diagnostic performance of the CellaVision preclassification neutrophil count - time to bypass the reclassification?

Development and Evaluation of an ELISA for Human Trefoil Factor 3

Use of cell‐free non‐invasive prenatal testing in pregnancies affected by placental mosaicism

Infant Ustekinumab Clearance, Risk of Infection, and Development After Exposure During Pregnancy

On the road to replacing invasive testing with cell‐based NIPT: Five clinical cases with aneuploidies, microduplication, unbalanced structural rearrangement, or mosaicism

A decade of change – lessons learned from prenatal diagnostics in Central Denmark region in 2008–2018

Fetal Heart Defects and Measures of Cerebral Size

Aggressive medullary thyroid carcinoma in a ten-year-old patient with multiple endocrine neoplasia 2B due to the A883F mutation

Influence of Lewis α1-3/4-L-Fucosyltransferase (FUT3) Gene Mutations on Enzyme Activity, Erythrocyte Phenotyping, and Circulating Tumor Marker Sialyl-Lewis a Levels

Placental mosaicism in the era of chromosomal microarrays

Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture

Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings

National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017

Prenatal diagnosis of Nager syndrome in a 12-week-old fetus with a whole gene deletion of SF3B4 by chromosomal microarray

Promoter hypomethylation and upregulation of trefoil factors in prostate cancer

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