Published in Anticancer Res on August 04, 2006
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci U S A (2004) 7.55
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging. Proc Natl Acad Sci U S A (2006) 3.86
Transcription factor E2-2 is an essential and specific regulator of plasmacytoid dendritic cell development. Cell (2008) 3.12
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci U S A (2006) 2.28
Tomographic molecular imaging and 3D quantification within adult mouse organs. Nat Methods (2006) 2.23
Telomere length and heredity: Indications of paternal inheritance. Proc Natl Acad Sci U S A (2005) 2.10
High-resolution three-dimensional imaging of islet-infiltrate interactions based on optical projection tomography assessments of the intact adult mouse pancreas. J Biomed Opt (2008) 1.88
A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception. Hum Mol Genet (2004) 1.86
The enlarged population of marginal zone/CD1d(high) B lymphocytes in nonobese diabetic mice maps to diabetes susceptibility region Idd11. J Immunol (2005) 1.72
Improved pharmacological therapy of chronic heart failure in primary care: a randomized Study of NT-proBNP Guided Management of Heart Failure--SIGNAL-HF (Swedish Intervention study--Guidelines and NT-proBNP AnaLysis in Heart Failure). Eur J Heart Fail (2010) 1.61
Quantification and three-dimensional imaging of the insulitis-induced destruction of beta-cells in murine type 1 diabetes. Diabetes (2010) 1.50
Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging. Eur J Hum Genet (2009) 1.34
Prevention of diabetes in nonobese diabetic mice mediated by CD1d-restricted nonclassical NKT cells. J Immunol (2004) 1.31
The peri-islet basement membrane, a barrier to infiltrating leukocytes in type 1 diabetes in mouse and human. Diabetes (2012) 1.27
Adoptive transfer of immunomodulatory M2 macrophages prevents type 1 diabetes in NOD mice. Diabetes (2012) 1.25
Polycomb target genes are silenced in multiple myeloma. PLoS One (2010) 1.21
Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population. Stroke (2005) 1.20
Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease. J Cell Sci (2008) 1.12
TCF7L2 polymorphisms are associated with type 2 diabetes in northern Sweden. Eur J Hum Genet (2007) 1.11
Distinct phenotype and function of NK cells in the pancreas of nonobese diabetic mice. J Immunol (2010) 1.08
CT60 genotype does not affect CTLA-4 isoform expression despite association to T1D and AITD in northern Sweden. BMC Med Genet (2007) 1.08
Beta-cell specific deletion of Dicer1 leads to defective insulin secretion and diabetes mellitus. PLoS One (2011) 1.04
Stochastic monoallelic expression of IL-10 in T cells. J Immunol (2006) 1.04
Identification of two cerebral malaria resistance loci using an inbred wild-derived mouse strain. Proc Natl Acad Sci U S A (2002) 1.03
The genetic population structure of northern Sweden and its implications for mapping genetic diseases. Hereditas (2007) 0.97
CD4(+) type II NKT cells mediate ICOS and programmed death-1-dependent regulation of type 1 diabetes. J Immunol (2012) 0.96
Stem cell depletion in Hutchinson-Gilford progeria syndrome. Aging Cell (2011) 0.96
Normalized endothelial function but sustained cardiovascular risk profile 11 years following a pregnancy complicated by preeclampsia. Hypertens Res (2013) 0.94
Near infrared optical projection tomography for assessments of β-cell mass distribution in diabetes research. J Vis Exp (2013) 0.94
Health effects on leaders and co-workers of an art-based leadership development program. Psychother Psychosom (2010) 0.89
A quality assessment survey of SNP genotyping laboratories. Hum Mutat (2006) 0.89
Characterization of lamin mutation phenotypes in Drosophila and comparison to human laminopathies. PLoS One (2007) 0.89
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia. Hum Mutat (2013) 0.89
The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease. Eur J Hum Genet (2003) 0.88
Expression of the Hutchinson-Gilford progeria mutation during osteoblast development results in loss of osteocytes, irregular mineralization, and poor biomechanical properties. J Biol Chem (2012) 0.87
Defective induction of CTLA-4 in the NOD mouse is controlled by the NOD allele of Idd3/IL-2 and a novel locus (Ctex) telomeric on chromosome 1. Diabetes (2006) 0.87
Homozygosity mapping of familial glioma in Northern Sweden. Acta Oncol (2005) 0.87
The Brichos domain of prosurfactant protein C can hold and fold a transmembrane segment. Protein Sci (2009) 0.86
Variation in the Cd3 zeta (Cd247) gene correlates with altered T cell activation and is associated with autoimmune diabetes. J Immunol (2010) 0.86
E2-2 regulates the expansion of pro-B cells and follicular versus marginal zone decisions. J Immunol (2006) 0.86
Low and high expressing alleles of the LMNA gene: implications for laminopathy disease development. PLoS One (2011) 0.85
Intron-mediated expression of the human neuropeptide Y Y1 receptor. Mol Cell Endocrinol (2002) 0.85
Plasminogen activator inhibitor-1 4G/5G polymorphism and risk of stroke: replicated findings in two nested case-control studies based on independent cohorts. Stroke (2005) 0.85
Embryonic expression of the common progeroid lamin A splice mutation arrests postnatal skin development. Aging Cell (2014) 0.85
Imaging dynamics of CD11c⁺ cells and Foxp3⁺ cells in progressive autoimmune insulitis in the NOD mouse model of type 1 diabetes. Diabetologia (2013) 0.85
Evidence for the involvement of lamins in aging. Curr Aging Sci (2010) 0.84
Differential expression of A-type and B-type lamins during hair cycling. PLoS One (2009) 0.84
Genome-wide linkage scan of common stroke in families from northern Sweden. Stroke (2006) 0.84
Analysis of NR3A receptor subunits in human native NMDA receptors. Brain Res (2007) 0.84
A role for E2-2 at the DN3 stage of early thymopoiesis. Mol Immunol (2008) 0.83
Remodeling of the innervation of pancreatic islets accompanies insulitis preceding onset of diabetes in the NOD mouse. J Neuroimmunol (2005) 0.83
Beneficial therapeutic effects of physical training and relaxation therapy in women with coronary syndrome X. Physiother Res Int (2002) 0.82
The Idd6.2 diabetes susceptibility region controls defective expression of the Lrmp gene in nonobese diabetic (NOD) mice. Immunogenetics (2007) 0.81
Overexpression of extracellular-SOD in islets of nonobese diabetic mice and development of diabetes. Free Radic Biol Med (2002) 0.81
Diabetes protection and restoration of thymocyte apoptosis in NOD Idd6 congenic strains. Diabetes (2003) 0.80
A previously functional tetracycline-regulated transactivator fails to target gene expression to the bone. BMC Res Notes (2011) 0.79
Linkage but not association of calpain-10 to type 2 diabetes replicated in northern Sweden. Diabetes (2006) 0.79
hTERT promoter methylation and telomere length in childhood acute lymphoblastic leukemia: associations with immunophenotype and cytogenetic subgroup. Exp Hematol (2011) 0.79
Unique genetic variation revealed by a microsatellite polymorphism survey in ten wild-derived inbred strains. Genomics (2002) 0.79
The NOD allele of the Idd5 locus on chromosome 1 mediates a non-cell-autonomous defect in negative selection of T cells. J Autoimmun (2007) 0.79
Fish oil delays lymphoma progression in the TLL mouse. Leuk Lymphoma (2010) 0.77
U-EPX levels and wheezing in infants and young children with and without RSV bronchiolitis. Respir Med (2005) 0.76
Organization of the chemosensory neuroepithelium of the vomeronasal organ of the Scandinavian moose Alces alces. Brain Res (2009) 0.76
Expression of the NK-1 receptor on islet cells and invading immune cells in the non-obese diabetic mouse. J Autoimmun (2005) 0.76
Lymphoblastic T-cell lymphoma in mice is unaffected by Celecoxib as single agent or in combination with cyclophosphamide. Leuk Lymphoma (2009) 0.76
Global and 3D spatial assessment of neuroinflammation in rodent models of Multiple Sclerosis. PLoS One (2013) 0.75
Dynamics of the immune response against extracellular products of group A streptococci during infection. Clin Vaccine Immunol (2006) 0.75
Exit of pediatric pre-B acute lymphoblastic leukaemia cells from the bone marrow to the peripheral blood is not associated with cell maturation or alterations in gene expression. Mol Cancer (2008) 0.75
Improving signal detection in emission optical projection tomography via single source multi-exposure image fusion. Opt Express (2013) 0.75
Dmu expression causes enrichment of MZ B cells, but is non permissive for B cell maturation in Rag2-/- mice even if combined with Bcl-2. Mol Immunol (2006) 0.75
Antitumor activity of the angiogenesis inhibitor TNP-470 on murine lymphoma/leukemia cells in vivo and in vitro. Exp Hematol (2003) 0.75
Delegation within municipal health care. J Nurs Manag (2011) 0.75
Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG. Neurosci Lett (2005) 0.75