Method of the concrete equivalent mortar (CEM)—A new tool to design concrete containing admixture
A Schwartzentruber, C Catherine - Materials and Structures, 2000 - Springer
This paper deals with a new method to design concrete containing admixture. Its principle is
to design a mortar, deduced from the concrete composition and called concrete equivalent …
to design a mortar, deduced from the concrete composition and called concrete equivalent …
Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease
…, S Mihaylov, C Sandor, A Schwartzentruber… - Progress in …, 2020 - Elsevier
Mechanistic disease stratification will be crucial to develop a precision medicine approach
for future disease modifying therapy in sporadic Parkinson’s disease (sPD). Mitochondrial …
for future disease modifying therapy in sporadic Parkinson’s disease (sPD). Mitochondrial …
Effect of PVA, glass and metallic fibers, and of an expansive admixture on the cracking tendency of ultrahigh strength mortar
A Schwartzentruber, M Philippe, G Marchese - Cement and Concrete …, 2004 - Elsevier
Ultrahigh strength mortars (UHSM) are new materials with high compressive and tensile
strengths. For such materials, autogenous shrinkage can sometimes induces cracks in …
strengths. For such materials, autogenous shrinkage can sometimes induces cracks in …
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
…, RL Conway, J St-Onge, JA Schwartzentruber… - Nature …, 2012 - nature.com
Megalencephaly-capillary malformation (MCAP) and megalencephaly-polymicrogyria-polydactyly-hydrocephalus
(MPPH) syndromes are sporadic overgrowth disorders associated …
(MPPH) syndromes are sporadic overgrowth disorders associated …
[HTML][HTML] Oxidative switch drives mitophagy defects in dopaminergic parkin mutant patient neurons
A Schwartzentruber, C Boschian, FM Lopes… - Scientific reports, 2020 - nature.com
Mutations in PRKN are the most common cause of early onset Parkinson’s disease. Parkin is
an E3 ubiquitin ligase, functioning in mitophagy. Mitochondrial abnormalities are present in …
an E3 ubiquitin ligase, functioning in mitophagy. Mitochondrial abnormalities are present in …
Rheological behaviour of fresh cement pastes formulated from a Self Compacting Concrete (SCC)
LDA Schwartzentruber, R Le Roy, J Cordin - Cement and Concrete …, 2006 - Elsevier
Self Compacting Concrete (SCC) has a high flowability and can be placed without vibration.
It is defined as a concrete that exhibits a high deformability and a good resistance to …
It is defined as a concrete that exhibits a high deformability and a good resistance to …
Microbiological quality of some spices and herbs in retail markets
…, AD Harpestad, A Swartzentruber… - Applied and …, 1982 - Am Soc Microbiol
The microbiological quality of 10 spices or herbs was determined by a national survey at the
retail level. Aerobic plate count values for the 10 products ranged from less than 100 to 3.1 …
retail level. Aerobic plate count values for the 10 products ranged from less than 100 to 3.1 …
[PDF][PDF] Mutations in PIK3R1 cause SHORT syndrome
…, AC Smith, D Alcantara, JA Schwartzentruber… - The American Journal of …, 2013 - cell.com
SHORT syndrome is a rare, multisystem disease characterized by short stature, anterior-chamber
eye anomalies, characteristic facial features, lipodystrophy, hernias, hyperextensibility, …
eye anomalies, characteristic facial features, lipodystrophy, hernias, hyperextensibility, …
[HTML][HTML] Loss of IGF1R in human astrocytes alters complex I activity and support for neurons
…, PR Heath, H Mortiboys, A Schwartzentruber… - Neuroscience, 2018 - Elsevier
The insulin/insulin-like growth factor 1 (IGF1) signaling pathways are implicated in longevity
and in progression of Alzheimer’s disease. Previously, we showed that insulin-like growth …
and in progression of Alzheimer’s disease. Previously, we showed that insulin-like growth …
[PDF][PDF] Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome
Genitopatellar syndrome (GPS) is a skeletal dysplasia with cerebral and genital anomalies
for which the molecular basis has not yet been determined. By exome sequencing, we found …
for which the molecular basis has not yet been determined. By exome sequencing, we found …