Somatic genome variations in vascular tissues and peripheral blood leukocytes in patients with atherosclerosis

Copy Number Variants: Distribution in Patients with Coronary Atherosclerosis

(2014) K. Gancheva et al.   BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT

Production of Type VI Collagen by Human Macrophages: A New Dimension in Macrophage Functional Heterogeneity

(2014) M. Schnoor et al.   JOURNAL OF IMMUNOLOGY

Republished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime

(2013) Lars Anders Forsberg et al.   POSTGRADUATE MEDICAL JOURNAL

The Src Substrate SKAP2 Regulates Actin Assembly by Interacting with WAVE2 and Cortactin Proteins

(2012) Shintaro Shimamura et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangement

(2012) Francis J. Alenghat et al.   JOURNAL OF CELL SCIENCE

Detectable clonal mosaicism and its relationship to aging and cancer

(2012) Kevin B Jacobs et al.   NATURE GENETICS

Detectable clonal mosaicism from birth to old age and its relationship to cancer

(2012) Cathy C Laurie et al.   NATURE GENETICS

Extensive genetic variation in somatic human tissues

(2012) M. O'Huallachain et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genetic copy number variants in myocardial infarction patients with hyperlipidemia

(2011) Wei-Chung Shia et al.   BMC GENOMICS

Alterations of RASSF1A in premalignant cervical lesions: Clinical and prognostic significance

(2011) Sraboni Mitra et al.   MOLECULAR CARCINOGENESIS

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

(2010) C. O'Keefe et al.   BLOOD

Selection and mutation in the “new” genetics: an emerging hypothesis

(2010) Bruce Gottlieb et al.   HUMAN GENETICS

Integrin-Induced PIP5K1C Kinase Polarization Regulates Neutrophil Polarization, Directionality, and In Vivo Infiltration

(2010) Wenwen Xu et al.   IMMUNITY

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

(2010)   NATURE

Missing heritability and strategies for finding the underlying causes of complex disease

(2010) Evan E. Eichler et al.   NATURE REVIEWS GENETICS

Control of cell proliferation in atherosclerosis: insights from animal models and human studies

(2009) J. J. Fuster et al.   CARDIOVASCULAR RESEARCH

From germline towards somatic mutations in the pathophysiology of vascular anomalies

(2009) N. Limaye et al.   HUMAN MOLECULAR GENETICS

What is paradominant inheritance?

(2009) R Happle   JOURNAL OF MEDICAL GENETICS

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

(2009) Sekar Kathiresan et al.   NATURE GENETICS

Somatic mosaicism for copy number variation in differentiated human tissues

(2008) Arkadiusz Piotrowski et al.   HUMAN MUTATION

Identification of DNA copy number aberrations by array comparative genomic hybridization in patients with ruptured intracranial aneurysms

(2008) Jin Soo Choi et al.   JOURNAL OF CLINICAL NEUROSCIENCE

Regulation of Endothelial Cell Cytoskeletal Reorganization by a Secreted Frizzled-Related Protein-1 and Frizzled 4- and Frizzled 7-Dependent Pathway

(2007) Pascale Dufourcq et al.   AMERICAN JOURNAL OF PATHOLOGY