Mice that express farnesylated versions of prelamin A in neurons develop achalasia

Expression of progerin in aging mouse brains reveals structural nuclear abnormalities without detectible significant alterations in gene expression, hippocampal stem cells or behavior

(2014) Jean-Ha Baek et al.   HUMAN MOLECULAR GENETICS

Murine genetic deficiency of neuronal nitric oxide synthase (nNOS-/-) and interstitial cells of Cajal (W/Wv): Implications for achalasia?

(2014) Michaela Müller et al.   JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY

Dominant role of interstitial cells of Cajal in nitrergic relaxation of murine lower oesophageal sphincter

(2014) Dieter Groneberg et al.   JOURNAL OF PHYSIOLOGY-LONDON

LINCing lamin B2 to neuronal migration

(2014) Catherine Coffinier et al.   Nucleus

Human iPSC-Based Modeling of Late-Onset Disease via Progerin-Induced Aging

(2013) Justine D. Miller et al.   Cell Stem Cell

New Lmna knock-in mice provide a molecular mechanism for the ‘segmental aging’ in Hutchinson–Gilford progeria syndrome†

(2013) Hea-Jin Jung et al.   HUMAN MOLECULAR GENETICS

Understanding the Roles of Nuclear A- and B-type Lamins in Brain Development

(2012) Stephen G. Young et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Nuclear Lamins in the Brain — New Insights into Function and Regulation

(2012) Hea-Jin Jung et al.   MOLECULAR NEUROBIOLOGY

Regulation of prelamin A but not lamin C by miR-9, a brain-specific microRNA

(2012) H.-J. Jung et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Pathogenesis of achalasia cardia

(2012) Uday C Ghoshal   WORLD JOURNAL OF GASTROENTEROLOGY

Hutchinson-gilford progeria is a skeletal dysplasia

(2011) Catherine M Gordon et al.   JOURNAL OF BONE AND MINERAL RESEARCH

MicroRNA-9 Regulates Neurogenesis in Mouse Telencephalon by Targeting Multiple Transcription Factors

(2011) M. Shibata et al.   JOURNAL OF NEUROSCIENCE

Deficiencies in lamin B1 and lamin B2 cause neurodevelopmental defects and distinct nuclear shape abnormalities in neurons

(2011) Catherine Coffinier et al.   MOLECULAR BIOLOGY OF THE CELL

MicroRNA-mediated conversion of human fibroblasts to neurons

(2011) Andrew S. Yoo et al.   NATURE

Von Mäusen und Menschen: Lsc/p115 und die Achalasie

(2011) H. Gockel et al.   ZEITSCHRIFT FUR GASTROENTEROLOGIE

Pathogenesis of Achalasia: Lessons From Mutant Mice

(2010) Raj K. Goyal et al.   GASTROENTEROLOGY

Achalasia: will genetic studies provide insights?

(2010) Henning R. Gockel et al.   HUMAN GENETICS

An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria

(2010) B. S. J. Davies et al.   HUMAN MOLECULAR GENETICS

Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiency

(2010) C. Coffinier et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Megaoesophagus inRassf1a-null mice

(2009) Louise van der Weyden et al.   INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY

Reduction of Interstitial Cells of Cajal (ICC) Associated With Neuronal Nitric Oxide Synthase (n-NOS) in Patients With Achalasia

(2008) Ines Gockel et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

Eliminating the Synthesis of Mature Lamin A Reduces Disease Phenotypes in Mice Carrying a Hutchinson-Gilford Progeria Syndrome Allele

(2008) Shao H. Yang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Progerin elicits disease phenotypes of progeria in mice whether or not it is farnesylated

(2008) Shao H. Yang et al.   JOURNAL OF CLINICAL INVESTIGATION