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The Nuclear Envelope as a Signaling Node in Development and Disease

Developmental cell, 2009-11, Vol.17 (5), p.626-638

2009

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Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene

Circulation (New York, N.Y.), 2011-01, Vol.123 (1), p.53-61

2011

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Biliary apotopes and anti‐mitochondrial antibodies activate innate immune responses in primary biliary cirrhosis

Hepatology (Baltimore, Md.), 2010-09, Vol.52 (3), p.987-998

2010

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Risk factors and comorbidities in primary biliary cirrhosis : A controlled interview-based study of 1032 patients

Hepatology (Baltimore, Md.), 2005-11, Vol.42 (5), p.1194-1202

2005

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Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery–Dreifuss muscular dystrophy

Human molecular genetics, 2007-08, Vol.16 (15), p.1884-1895

2007

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PBC Screen: An IgG/IgA dual isotype ELISA detecting multiple mitochondrial and nuclear autoantibodies specific for primary biliary cirrhosis

Journal of autoimmunity, 2010-12, Vol.35 (4), p.436-442

2010

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Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis

Hepatology (Baltimore, Md.), 2006-05, Vol.43 (5), p.1135-1144

2006

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Epithelial cell specificity and apotope recognition by serum autoantibodies in primary biliary cirrhosis

Hepatology (Baltimore, Md.), 2011-07, Vol.54 (1), p.196-203

2011

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Abnormal p38α mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

Human molecular genetics, 2012-10, Vol.21 (19), p.4325-4333

2012

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Molecular mimicry of mitochondrial and nuclear autoantigens in primary biliary cirrhosis

Gastroenterology (New York, N.Y. 1943), 2003-06, Vol.124 (7), p.1915-1925

2003

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Hepatic Steatosis in Dunnigan-Type Familial Partial Lipodystrophy

The American journal of gastroenterology, 2005-10, Vol.100 (10), p.2218-2224

2005

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Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins

Human molecular genetics, 2009-01, Vol.18 (2), p.241-247

2009

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Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

Cardiovascular research, 2012-02, Vol.93 (2), p.311-319

2012

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MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-β signaling

Human molecular genetics, 2005-02, Vol.14 (3), p.437-445

2005

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Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy

Human molecular genetics, 2006-02, Vol.15 (4), p.653-663

2006

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Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy

Human molecular genetics, 2006-08, Vol.15 (16), p.2479-2489

2006

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Perturbation of nuclear lamin A causes cell death in chondrocytes

Arthritis & rheumatology (Hoboken, N.J.), 2012-06, Vol.64 (6), p.1940-1949

2012

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Nuclear envelope proteins and neuromuscular diseases

Muscle & nerve, 2003-04, Vol.27 (4), p.393-406

2003

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Epidermal expression of the truncated prelamin A causing Hutchinson–Gilford progeria syndrome: effects on keratinocytes, hair and skin

Human molecular genetics, 2008-08, Vol.17 (15), p.2357-2369

2008

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Peroxisome Proliferator-Activated Receptor-γ C190S Mutation Causes Partial Lipodystrophy

The journal of clinical endocrinology and metabolism, 2007-06, Vol.92 (6), p.2248-2255

2007

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Anti-neutrophil antibodies in primary sclerosing cholangitis

Baillière's best practice & research. Clinical gastroenterology, 2001-08, Vol.15 (4), p.629-642

2001

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Quality of life and everyday activities in patients with primary biliary cirrhosis

Hepatology (Baltimore, Md.), 2007-12, Vol.46 (6), p.1836-1843

2007

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The Amino-Terminal Domain of the Lamin B Receptor Is a Nuclear Envelope Targeting Signal

The Journal of cell biology, 1993-03, Vol.120 (5), p.1093-1100

1993

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Structural Organization of the Human Gene (LMNB1) Encoding Nuclear Lamin B1

Genomics (San Diego, Calif.), 1995-05, Vol.27 (2), p.230-236

1995

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Nuclear lamins and laminopathies: The Cell Biology of Disease

The Journal of pathology, 2012, Vol.226 (2), p.316-325

WORMAN, Howard J

2012

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The Nuclear Envelope as a Signaling Node in Development and Disease

Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene

Biliary apotopes and anti‐mitochondrial antibodies activate innate immune responses in primary biliary cirrhosis

Risk factors and comorbidities in primary biliary cirrhosis : A controlled interview-based study of 1032 patients

Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery–Dreifuss muscular dystrophy

PBC Screen: An IgG/IgA dual isotype ELISA detecting multiple mitochondrial and nuclear autoantibodies specific for primary biliary cirrhosis

Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis

Epithelial cell specificity and apotope recognition by serum autoantibodies in primary biliary cirrhosis

Abnormal p38α mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

Molecular mimicry of mitochondrial and nuclear autoantigens in primary biliary cirrhosis

Hepatic Steatosis in Dunnigan-Type Familial Partial Lipodystrophy

Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins

Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-β signaling

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy

Perturbation of nuclear lamin A causes cell death in chondrocytes

Nuclear envelope proteins and neuromuscular diseases

Epidermal expression of the truncated prelamin A causing Hutchinson–Gilford progeria syndrome: effects on keratinocytes, hair and skin

Peroxisome Proliferator-Activated Receptor-γ C190S Mutation Causes Partial Lipodystrophy

Anti-neutrophil antibodies in primary sclerosing cholangitis

Quality of life and everyday activities in patients with primary biliary cirrhosis

The Amino-Terminal Domain of the Lamin B Receptor Is a Nuclear Envelope Targeting Signal

Structural Organization of the Human Gene (LMNB1) Encoding Nuclear Lamin B1

Nuclear lamins and laminopathies: The Cell Biology of Disease

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