List of works - Jacqueline de Belleroche

A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.

scientific article

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

scientific article published on 15 April 2016

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

scientific article published on 22 October 2014

Extracellular release of the atheroprotective heat shock protein 27 is mediated by estrogen and competitively inhibits acLDL binding to scavenger receptor-A.

scientific article published on 19 June 2008

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

scientific article

Heat shock protein 27 attenuates neointima formation and accelerates reendothelialization after arterial injury and stent implantation: importance of vascular endothelial growth factor up-regulation.

scientific article

Heat shock protein 27 overexpression mitigates cytokine-induced islet apoptosis and streptozotocin-induced diabetes

scientific article published on 26 March 2009

Heat shock protein 27 protects against atherogenesis via an estrogen-dependent mechanism: role of selective estrogen receptor beta modulation.

scientific article published on 3 September 2009

Heat shock protein 27 rescues motor neurons following nerve injury and preserves muscle function

scientific journal article

Identification of PEX7 as the second gene involved in Refsum disease

scientific article

Investigation of G72 (DAOA) expression in the human brain

scientific article

Mice that overexpress human heat shock protein 27 have increased renal injury following ischemia reperfusion

scientific article

Pathogenesis of Parkinson's disease: emerging role of molecular chaperones

scientific article published on 24 December 2009

Serum heat shock protein 27 levels represent a potential therapeutic target for atherosclerosis: observations from a human cohort and treatment of female mice.

scientific article published on 10 June 2013

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

scientific article

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

scientific article

The neuroprotective effects of heat shock protein 27 overexpression in transgenic animals against kainate-induced seizures and hippocampal cell death

scientific journal article

The role of d-amino acids in amyotrophic lateral sclerosis pathogenesis: a review ⬇️

scientific article published on August 14, 2012

List of works by Jacqueline de Belleroche

A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

Extracellular release of the atheroprotective heat shock protein 27 is mediated by estrogen and competitively inhibits acLDL binding to scavenger receptor-A.

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

Heat shock protein 27 attenuates neointima formation and accelerates reendothelialization after arterial injury and stent implantation: importance of vascular endothelial growth factor up-regulation.

Heat shock protein 27 overexpression mitigates cytokine-induced islet apoptosis and streptozotocin-induced diabetes

Heat shock protein 27 protects against atherogenesis via an estrogen-dependent mechanism: role of selective estrogen receptor beta modulation.

Heat shock protein 27 rescues motor neurons following nerve injury and preserves muscle function

Identification of PEX7 as the second gene involved in Refsum disease

Investigation of G72 (DAOA) expression in the human brain

Mice that overexpress human heat shock protein 27 have increased renal injury following ischemia reperfusion

Pathogenesis of Parkinson's disease: emerging role of molecular chaperones

Serum heat shock protein 27 levels represent a potential therapeutic target for atherosclerosis: observations from a human cohort and treatment of female mice.

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

The neuroprotective effects of heat shock protein 27 overexpression in transgenic animals against kainate-induced seizures and hippocampal cell death

The role of d-amino acids in amyotrophic lateral sclerosis pathogenesis: a review ⬇️