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A hidden Markov model to assess drug-induced sleep fragmentation in the telemetered rat

Journal of pharmacokinetics and pharmacodynamics, 2011-12, Vol.38 (6), p.697-711

2011

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P.133 Paediatric dosing of balovaptan for the treatment of the core symptoms of autism spectrum disorder: data from a Phase 2 study (aV1ation; NCT02901431)

European neuropsychopharmacology, 2020-11, Vol.40, p.S82-S83

2020

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Pharmacokinetic–pharmacodynamic models for categorical toxicity data

Regulatory toxicology and pharmacology, 2005-02, Vol.41 (1), p.55-65

2005

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Convergence en moyenne quadratique de l'estimateur de la régression par splines hybrides

Comptes rendus de l'Académie des sciences. Série I. Mathématique, 1998, Vol.326 (5), p.615-618

1998

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Manifestations cardiovasculaires cliniques et électrocardiographiques au cours du tétanos : étude prospective à propos de 30 cas observés à la clinique des maladies infectieuses du CHU de Fann à Dakar

Médecine et maladies infectieuses, 2005-09, Vol.35 (9), p.450-454

2005

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Cardiovascular events in the course of tetanus: a prospective study on 30 cases in the infectious diseases clinic, in the Fann teaching hospital, Dakar

Médecine et maladies infectieuses, 2005-09, Vol.35 (9), p.450-454

2005

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Public health risks from subclinical variant CJD

PLoS pathogens, 2017-11, Vol.13 (11), p.e1006642-e1006642

2017

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Identification of a homology-independent linchpin domain controlling mouse and bank vole prion protein conversion

PLoS pathogens, 2020-09, Vol.16 (9), p.e1008875-e1008875

2020

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Unravelling the glial response in the pathogenesis of Alzheimer's disease

The FASEB journal, 2018-11, Vol.32 (11), p.5766-5777

2018

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Biomechanics of predator-prey arms race in lion, zebra, cheetah and impala

Nature (London), 2018-02, Vol.554 (7691), p.183-188

2018

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Insights into Mechanisms of Chronic Neurodegeneration

International Journal of Molecular Sciences, 2016-01, Vol.17 (1), p.82-82

2016

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Spermine increases acetylation of tubulins and facilitates autophagic degradation of prion aggregates

Scientific reports, 2018-07, Vol.8 (1), p.10004-17, Article 10004

2018

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No Adaptation of the Prion Strain in a Heterozygous Case of Variant Creutzfeldt-Jakob Disease

Emerging infectious diseases, 2020-06, Vol.26 (6), p.1300-1303

2020

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On the structure and electronic properties of Fe2V0.8W0.2Al thin films

Physical chemistry chemical physics : PCCP, 2020-01, Vol.22 (39), p.22549-22554

2020

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Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid-β or Pathologic Phenotype

PloS one, 2016-07, Vol.11 (7), p.e0159119

2016

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The Old-Celtic Inscribed and Sculptured Stone at Auquhollie, Kincardineshire, and Ogam in Scotland

Proceedings of the Society of Antiquaries of Scotland, 1925-11, Vol.59, p.257-269

Diack, Francis C

1925

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Place-Names, Highlands and Islands of Scotland

The Scottish Historical Review, 1923, Vol.21 (81), p.73-74

Diack, F. C.

1923

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Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties

Emerging infectious diseases, 2014-12, Vol.20 (12), p.1969-1979

2014

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Skinned fibres produce the same power and force as intact fibre bundles from muscle of wild rabbits

Journal of experimental biology, 2015-09, Vol.218 (Pt 18), p.2856-2863

2015

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Traits associated with innate and adaptive immunity in pigs: heritability and associations with performance under different health status conditions

Genetics selection evolution (Paris), 2009-12, Vol.41 (1), p.54-54, Article 54

2009

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The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between species

Journal of virology, 2015-05, Vol.89 (9), p.4738-4747

2015

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Similarities of Variant Creutzfeldt-Jakob Disease Strain in Mother and Son in Spain to UK Reference Case

Emerging infectious diseases, 2017-09, Vol.23 (9), p.1593-1596

2017

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Strain Typing of Prion Diseases Using In Vivo Mouse Models

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1658, p.263

2017

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Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes

Brain (London, England : 1878), 2019-05, Vol.142 (5), p.1416-1428

2019

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Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt―Jakob disease

Brain (London, England : 1878), 2013-04, Vol.136 (Pt 4), p.1139-1145

2013

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A hidden Markov model to assess drug-induced sleep fragmentation in the telemetered rat

P.133 Paediatric dosing of balovaptan for the treatment of the core symptoms of autism spectrum disorder: data from a Phase 2 study (aV1ation; NCT02901431)

Pharmacokinetic–pharmacodynamic models for categorical toxicity data

Convergence en moyenne quadratique de l'estimateur de la régression par splines hybrides

Manifestations cardiovasculaires cliniques et électrocardiographiques au cours du tétanos : étude prospective à propos de 30 cas observés à la clinique des maladies infectieuses du CHU de Fann à Dakar

Cardiovascular events in the course of tetanus: a prospective study on 30 cases in the infectious diseases clinic, in the Fann teaching hospital, Dakar

Public health risks from subclinical variant CJD

Identification of a homology-independent linchpin domain controlling mouse and bank vole prion protein conversion

Unravelling the glial response in the pathogenesis of Alzheimer's disease

Biomechanics of predator-prey arms race in lion, zebra, cheetah and impala

Insights into Mechanisms of Chronic Neurodegeneration

Spermine increases acetylation of tubulins and facilitates autophagic degradation of prion aggregates

No Adaptation of the Prion Strain in a Heterozygous Case of Variant Creutzfeldt-Jakob Disease

On the structure and electronic properties of Fe2V0.8W0.2Al thin films

Ablation of Prion Protein in Wild Type Human Amyloid Precursor Protein (APP) Transgenic Mice Does Not Alter The Proteolysis of APP, Levels of Amyloid-β or Pathologic Phenotype

The Old-Celtic Inscribed and Sculptured Stone at Auquhollie, Kincardineshire, and Ogam in Scotland

Place-Names, Highlands and Islands of Scotland

Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties

Skinned fibres produce the same power and force as intact fibre bundles from muscle of wild rabbits

Traits associated with innate and adaptive immunity in pigs: heritability and associations with performance under different health status conditions

The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between species

Similarities of Variant Creutzfeldt-Jakob Disease Strain in Mother and Son in Spain to UK Reference Case

Strain Typing of Prion Diseases Using In Vivo Mouse Models

Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt―Jakob disease

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