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Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome

author

Rodney Samaco

Alan K. Percy

Walter E Kaufmann

Jeffrey L. Neul

Daniel G Glaze

published in: PLOS One

date of publication: 2016-11-09

language: English

main subject: Rett syndrome, kidney failure

Cites articles 48

Date

Title

Authors

2016-03-06

Experimental models of renal calcium stones in rodents
2016-02-19

Lower urinary tract symptoms and urodynamic findings in children and adults with cerebral palsy: A systematic review

Johan Vande Walle, Piet Hoebeke, Erik Van Laecke
2015-01-01

Rate of urinary retention in adults with down syndrome: a prospective study.
2014-04-09

Spontaneous voiding by mice reveals strain-specific lower urinary tract function to be a quantitative genetic trait

William D. Steers, Gary A Churchill
2014-03-10

Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.
2013-11-25

Prevalence and Predictors of Urinary Tract Infections among Children with Cerebral Palsy in Makurdi, Nigeria
2013-07-28

A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome

Jay Shendure, David W. Russell
2013-08-09

Uroflowmetry in the management of lower urinary tract symptoms of children and adolescents with cerebral palsy.
2012-10-01

Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies

Rodney Samaco, Christopher S. Ward, Jeffrey L. Neul, Huda Zoghbi
2012-07-01

NIH Image to ImageJ: 25 years of image analysis

Kevin Eliceiri, Wayne Rasband
2011-12-01

Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome

Jose A Herrera, Christopher S. Ward, Jeffrey L. Neul, Xander H T Wehrens, Alan K. Percy, Daniel G Glaze
2011-07-01

MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan

Christopher S. Ward, Jeffrey L. Noebels, Jeffrey L. Neul, Teng-Wei Huang
2010-12

Rett syndrome: revised diagnostic criteria and nomenclature

Nadia Bahi-Buisson, Jeffrey L. Neul, John Christodoulou, Alessandra Renieri, Alan K. Percy, Walter E Kaufmann, Daniel G Glaze
2010-12-01

Rett syndrome diagnostic criteria: lessons from the Natural History Study

Jeffrey L. Neul, Alan K. Percy, Daniel G Glaze
2009-05-01

Urethral obstruction by seminal coagulum is associated with medetomidine-ketamine anesthesia in male mice on C57BL/6J and mixed genetic backgrounds
2008-10-15

Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance

Stanislas Lyonnet, Ivana Ricca, Jeanne Amiel, Orsetta Zuffardi, Annick Toutain
2008-03-12

Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome

Jeffrey L. Neul, Huda Zoghbi
2008-01-01

Voided stain on paper method for analysis of mouse urination.
2008-01-01

Lower urinary tract symptoms in dementia with Lewy bodies, Parkinson disease, and Alzheimer disease.

Werner Poewe
2007-10-01

Brain-derived neurotrophic factor expression and respiratory function improve after ampakine treatment in a mouse model of Rett syndrome
2007-07-01

Recurrent urinary tract infections in children: risk factors and association with prophylactic antimicrobials

Theoklis E. Zaoutis, Avital Cnaan
2007-02-23

Reversal of neurological defects in a mouse model of Rett syndrome

Adrian Peter Bird
2007-04-01

Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome

Laurent Villard, Jean-Christophe Roux
2006-04-01

Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice
2006-08-28

Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome

Jan-Marino Ramirez
2006-02-01

Renal stone epidemiology in Rochester, Minnesota: an update
2005-12-14

Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice

Jean-Christophe Roux, Andrew K Tryba, Jan-Marino Ramirez, Laurent Villard, Fernando Peña-Ortega
2003-01-01

Sexual dysfunction and sudden death in epileptic male EL mice: inheritance and prevention with the ketogenic diet

Thomas N. Seyfried, James G. Fox
2002-02-01

MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings.

Fons John Marie Gabreëls
2001-03

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

Rudolf Jaenisch
2001-03-01

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

Brian Hendrich, Adrian Peter Bird
1999-10-01

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Huda Zoghbi, Uta Francke

Article - wd:Q36187325

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