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Acid sphingomyelinase inhibition protects mice from lung edema and lethal Staphylococcus aureus sepsis

Journal of molecular medicine (Berlin, Germany), 2015-06, Vol.93 (6), p.675-689

2015

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Application of genomewide SNP arrays for detection of simulated susceptibility loci

Human mutation, 2005-06, Vol.25 (6), p.557-565

2005

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CD8+ T cells armed with retrovirally transduced IFN-γ

Journal of molecular medicine (Berlin, Germany), 2007-01, Vol.85 (1), p.63-73

2007

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A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes

Mammalian genome, 2020-02, Vol.31 (1-2), p.30-48

2020

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Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects

American journal of human genetics, 2009-12, Vol.85 (6), p.883-889

2009

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Effective population size of adult and offspring cohorts as a genetic monitoring tool in two stand-forming and wind-pollinated tree species: Fagus sylvatica L. and Picea abies (L.) Karst

Conservation genetics, 2024-06, Vol.25 (3), p.739-753

2024

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Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistance

Genome medicine, 2018-07, Vol.10 (1), p.55-55, Article 55

2018

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Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes

Human mutation, 2001-10, Vol.18 (4), p.327-336

2001

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Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation

European journal of human genetics : EJHG, 2011-12, Vol.19 (12), p.1281-1288

2011

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Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia

American journal of human genetics, 2008-04, Vol.82 (4), p.959-970

2008

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Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci

Human molecular genetics, 2012-01, Vol.21 (1), p.219-235

2012

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Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

Familial cancer, 2012-03, Vol.11 (1), p.19-26

2012

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Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta

American journal of human genetics, 2015-03, Vol.96 (3), p.432-439

2015

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Nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced pulmonary adenocarcinomas in Syrian golden hamsters contain beta 2-adrenergic receptor single-nucleotide polymorphisms

Genes chromosomes & cancer, 2005-10, Vol.44 (2), p.212-217

2005

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Parallel Structural Evolution of Mitochondrial Ribosomes and OXPHOS Complexes

Genome biology and evolution, 2015-05, Vol.7 (5), p.1235-1251

2015

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Rapid signalling by androgen receptor in prostate cancer cells

Oncogene, 1999-11, Vol.18 (46), p.6322-6329

1999

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Role of CD95 in pulmonary inflammation and infection in cystic fibrosis

Journal of molecular medicine (Berlin, Germany), 2012-09, Vol.90 (9), p.1011-1023

2012

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Acid sphingomyelinase inhibition protects mice from lung edema and lethal Staphylococcus aureus sepsis

Application of genomewide SNP arrays for detection of simulated susceptibility loci

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms

CD8+ T cells armed with retrovirally transduced IFN-γ

A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes

Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects

Effective population size of adult and offspring cohorts as a genetic monitoring tool in two stand-forming and wind-pollinated tree species: Fagus sylvatica L. and Picea abies (L.) Karst

Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistance

Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes

Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation

Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia

Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

Mutations in CCDC39 and CCDC40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms

Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta

Nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced pulmonary adenocarcinomas in Syrian golden hamsters contain beta 2-adrenergic receptor single-nucleotide polymorphisms

Parallel Structural Evolution of Mitochondrial Ribosomes and OXPHOS Complexes

Rapid signalling by androgen receptor in prostate cancer cells

Role of CD95 in pulmonary inflammation and infection in cystic fibrosis

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