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A lymphocyte–microglia–astrocyte axis in chronic active multiple sclerosis

Nature (London), 2021-09, Vol.597 (7878), p.709-714

2021

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LRP1 regulates peroxisome biogenesis and cholesterol homeostasis in oligodendrocytes and is required for proper CNS myelin development and repair

eLife, 2017-12, Vol.6

2017

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Serum Bilirubin and Genes Controlling Bilirubin Concentrations as Biomarkers for Cardiovascular Disease

Clinical chemistry (Baltimore, Md.), 2010-10, Vol.56 (10), p.1535-1543

2010

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Lipofuscin-like autofluorescence within microglia and its impact on studying microglial engulfment

Nature communications, 2023-11, Vol.14 (1), p.7060-7060, Article 7060

2023

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Transcriptomic architecture of nuclei in the marmoset CNS

Nature communications, 2022-09, Vol.13 (1), p.5531-5531, Article 5531

2022

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Association between the UGT1A128 allele, bilirubin levels, and coronary heart disease in the framingham heart study

Circulation (New York, N.Y.), 2006-10, Vol.114 (14), p.1476-1481

2006

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Serum Vascular Endothelial Growth Factor-D Levels in Patients With Lymphangioleiomyomatosis Reflect Lymphatic Involvement

Chest, 2009-05, Vol.135 (5), p.1293-1300

2009

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Genome-wide association meta-analysis for total serum bilirubin levels

Human molecular genetics, 2009-07, Vol.18 (14), p.2700-2710

2009

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Inhibition of Bcl-2 improves effect of LCL161, a SMAC mimetic, in hepatocellular carcinoma cells

Biochemical pharmacology, 2012-08, Vol.84 (3), p.268-277

2012

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PI(3,5)P2 biosynthesis regulates oligodendrocyte differentiation by intrinsic and extrinsic mechanisms

eLife, 2016-03, Vol.5

2016

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Wnt5b integrates Fak1a to mediate gastrulation cell movements via Rac1 and Cdc42

Open biology, 2020-02, Vol.10 (2), p.190273

2020

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Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels—The Framingham Heart Study

Atherosclerosis, 2009-09, Vol.206 (1), p.228-233

2009

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Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study

BMC medical genetics, 2007-09, Vol.8 Suppl 1 (S1), p.S12-S12, Article S12

2007

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Ultrahigh-resolution MRI Reveals Extensive Cortical Demyelination in a Nonhuman Primate Model of Multiple Sclerosis

Cerebral cortex (New York, N.Y. 1991), 2021-01, Vol.31 (1), p.439-447

2021

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Evidence for linkage of red blood cell size and count: Genome‐wide scans in the Framingham Heart Study

American journal of hematology, 2007-07, Vol.82 (7), p.605-610

2007

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Genetic and morphologic determinants of pneumothorax in lymphangioleiomyomatosis

American journal of physiology. Lung cellular and molecular physiology, 2007-09, Vol.293 (3), p.L800-L808

2007

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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

Nature genetics, 2009-11, Vol.41 (11), p.1191-1198

2009

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The C/A(-18) polymorphism in the surfactant protein B gene influences transcription and protein levels of surfactant protein B

American journal of physiology. Lung cellular and molecular physiology, 2007-02, Vol.292 (2), p.L448-L453

2007

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Protective role of the lipid phosphatase Fig4 in the adult nervous system

Human molecular genetics, 2018-07, Vol.27 (14), p.2443-2453

2018

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Mitophagy-related gene signature predicts prognosis, immune infiltration and chemotherapy sensitivity in colorectal cancer

World journal of gastrointestinal oncology, 2023-03, Vol.15 (3), p.546-561

2023

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Phenotypic characterization of disseminated cells with TSC2 loss of heterozygosity in patients with lymphangioleiomyomatosis

American journal of respiratory and critical care medicine, 2010-12, Vol.182 (11), p.1410-1418

2010

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Osteoprotegerin Contributes to the Metastatic Potential of Cells with a Dysfunctional TSC2 Tumor-Suppressor Gene

The American journal of pathology, 2013-09, Vol.183 (3), p.938-950

2013

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Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex

Human molecular genetics, 2000-12, Vol.9 (20), p.3037-3046

2000

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Correction to 'Wnt5b integrates Fak1a to mediate gastrulation cell movements via Rac1 and Cdc42'

Open biology, 2020-03, Vol.10 (3), p.200058-200058

2020

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Heritability of serum γ-glutamyltransferase level: genetic analysis from the Framingham Offspring Study

Liver international, 2009-05, Vol.29 (5), p.776-777

2009

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A lymphocyte–microglia–astrocyte axis in chronic active multiple sclerosis

LRP1 regulates peroxisome biogenesis and cholesterol homeostasis in oligodendrocytes and is required for proper CNS myelin development and repair

Serum Bilirubin and Genes Controlling Bilirubin Concentrations as Biomarkers for Cardiovascular Disease

Lipofuscin-like autofluorescence within microglia and its impact on studying microglial engulfment

Transcriptomic architecture of nuclei in the marmoset CNS

Association between the UGT1A128 allele, bilirubin levels, and coronary heart disease in the framingham heart study

Serum Vascular Endothelial Growth Factor-D Levels in Patients With Lymphangioleiomyomatosis Reflect Lymphatic Involvement

Genome-wide association meta-analysis for total serum bilirubin levels

Inhibition of Bcl-2 improves effect of LCL161, a SMAC mimetic, in hepatocellular carcinoma cells

PI(3,5)P2 biosynthesis regulates oligodendrocyte differentiation by intrinsic and extrinsic mechanisms

Wnt5b integrates Fak1a to mediate gastrulation cell movements via Rac1 and Cdc42

Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels—The Framingham Heart Study

Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study

Ultrahigh-resolution MRI Reveals Extensive Cortical Demyelination in a Nonhuman Primate Model of Multiple Sclerosis

Evidence for linkage of red blood cell size and count: Genome‐wide scans in the Framingham Heart Study

Genetic and morphologic determinants of pneumothorax in lymphangioleiomyomatosis

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

The C/A(-18) polymorphism in the surfactant protein B gene influences transcription and protein levels of surfactant protein B

Protective role of the lipid phosphatase Fig4 in the adult nervous system

Mitophagy-related gene signature predicts prognosis, immune infiltration and chemotherapy sensitivity in colorectal cancer

Phenotypic characterization of disseminated cells with TSC2 loss of heterozygosity in patients with lymphangioleiomyomatosis

Osteoprotegerin Contributes to the Metastatic Potential of Cells with a Dysfunctional TSC2 Tumor-Suppressor Gene

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex

Correction to 'Wnt5b integrates Fak1a to mediate gastrulation cell movements via Rac1 and Cdc42'

Heritability of serum γ-glutamyltransferase level: genetic analysis from the Framingham Offspring Study

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