List of works - Claire L Navarro

A New Lamin A Mutation Associated with Acrogeria Syndrome

scientific article published on 01 April 2014

A conserved splicing mechanism of the LMNA gene controls premature aging.

scientific article published on 29 August 2011

A-type lamins and progeroïd syndromes : persistent farnesylation with dramatic effects

scientific article

Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model.

scientific article

An inheritedLMNAgene mutation in atypical Progeria syndrome

scientific article published on 18 September 2012

Antisense-Based Progerin Downregulation in HGPS-Like Patients' Cells

scientific article published on 11 July 2016

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging.

scientific article

Drug screening on Hutchinson Gilford progeria pluripotent stem cells reveals aminopyrimidines as new modulators of farnesylation.

scientific article

Full-length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells

scientific article published on 8 October 2013

Identification of different genomic deletions and one duplication in the dysferlin gene using multiplex ligation-dependent probe amplification and genomic quantitative PCR.

scientific article

Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome

scientific article published on 05 March 2014

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

scientific article

Lamin a truncation in Hutchinson-Gilford progeria.

scientific article

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors.

scientific article

MG132-induced progerin clearance is mediated by autophagy activation and splicing regulation.

scientific article published on 3 July 2017

Molecular bases of progeroid syndromes.

scientific article

New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update

scientific article

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

scientific article published on 22 March 2014

Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.

scientific article

Splicing-Directed Therapy in a New Mouse Model of Human Accelerated Aging

article

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

scientific article published on 4 February 2015

Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation

scientific article

Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNA

scientific article published on 21 June 2012

Vulnerability of progeroid smooth muscle cells to biomechanical forces is mediated by MMP13

scientific article published on 17 August 2020

miR-9: the sentinel of neurons in progeria

scientific article

List of works by Claire L Navarro

A New Lamin A Mutation Associated with Acrogeria Syndrome

A conserved splicing mechanism of the LMNA gene controls premature aging.

A-type lamins and progeroïd syndromes : persistent farnesylation with dramatic effects

Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model.

An inheritedLMNAgene mutation in atypical Progeria syndrome

Antisense-Based Progerin Downregulation in HGPS-Like Patients' Cells

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging.

Drug screening on Hutchinson Gilford progeria pluripotent stem cells reveals aminopyrimidines as new modulators of farnesylation.

Full-length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells

Identification of different genomic deletions and one duplication in the dysferlin gene using multiplex ligation-dependent probe amplification and genomic quantitative PCR.

Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

Lamin a truncation in Hutchinson-Gilford progeria.

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors.

MG132-induced progerin clearance is mediated by autophagy activation and splicing regulation.

Molecular bases of progeroid syndromes.

New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.

Splicing-Directed Therapy in a New Mouse Model of Human Accelerated Aging

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation

Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNA

Vulnerability of progeroid smooth muscle cells to biomechanical forces is mediated by MMP13

miR-9: the sentinel of neurons in progeria