Lista de obras - Hayley Crawford - Dominio Público Uruguay

A Behavioural Assessment of Social Anxiety and Social Motivation in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes

artículo científico publicado en 2020

Adaptation of HIV-1 to human leukocyte antigen class I

artículo científico publicado en 2009

An experimental study of executive function and social impairment in Cornelia de Lange syndrome.

artículo científico publicado en 2017

BDNF Val(66)Met and 5-HTTLPR Genotype are Each Associated with Visual Scanning Patterns of Faces in Young Children

artículo científico publicado en 2015

CD8+ T-cell responses to different HIV proteins have discordant associations with viral load

artículo científico publicado en 2006

Central role of reverting mutations in HLA associations with human immunodeficiency virus set point

artículo científico publicado en 2008

Compensatory mutation partially restores fitness and delays reversion of escape mutation within the immunodominant HLA-B*5703-restricted Gag epitope in chronic human immunodeficiency virus type 1 infection

artículo científico publicado en 2007

Control of human immunodeficiency virus type 1 is associated with HLA-B*13 and targeting of multiple gag-specific CD8+ T-cell epitopes

artículo científico publicado en 2007

Correction for Thobakgale et al., Impact of HLA in Mother and Child on Disease Progression of Pediatric Human Immunodeficiency Virus Type 1 Infection

artículo científico publicado en 2015

Differential effects of anxiety and autism on social scene scanning in males with fragile X syndrome.

artículo científico publicado en 2017

Differential selection pressure exerted on HIV by CTL targeting identical epitopes but restricted by distinct HLA alleles from the same HLA supertype

artículo científico publicado en 2006

Diverse Profiles of Anxiety Related Disorders in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes

artículo científico publicado en 2017

Evolution of HLA-B5703 HIV-1 escape mutations in HLA-B5703-positive individuals and their transmission recipients

artículo científico publicado en 2009

Face scanning and spontaneous emotion preference in Cornelia de Lange syndrome and Rubinstein-Taybi syndrome.

artículo científico publicado en 2015

Fitness cost of escape mutations in p24 Gag in association with control of human immunodeficiency virus type 1

artículo científico publicado en 2006

Genetic modifiers in rare disorders: the case of fragile X syndrome

scientific article published on 29 August 2020

HLA class I-driven evolution of human immunodeficiency virus type 1 subtype c proteome: immune escape and viral load

artículo científico publicado en 2008

HLA footprints on human immunodeficiency virus type 1 are associated with interclade polymorphisms and intraclade phylogenetic clustering

artículo científico publicado en 2009

Impact of HLA in mother and child on disease progression of pediatric human immunodeficiency virus type 1 infection

artículo científico publicado en 2009

Implicit Discrimination of Basic Facial Expressions of Positive/Negative Emotion in Fragile X Syndrome and Autism Spectrum Disorder.

artículo científico publicado en 2015

Infant Social Avoidance Predicts Autism but Not Anxiety in Fragile X Syndrome

artículo científico publicado en 2019

Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis.

artículo científico publicado en 2019

Mutually exclusive T-cell receptor induction and differential susceptibility to human immunodeficiency virus type 1 mutational escape associated with a two-amino-acid difference between HLA class I subtypes

artículo científico publicado en 2006

Overactivity, impulsivity and repetitive behaviour in males with fragile X syndrome: contrasting developmental trajectories in those with and without elevated autism symptoms

scientific article published on 03 May 2018

Proliferative capacity of epitope-specific CD8 T-cell responses is inversely related to viral load in chronic human immunodeficiency virus type 1 infection

artículo científico publicado en 2006

Social Avoidance Emerges in Infancy and Persists into Adulthood in Fragile X Syndrome

scientific article published on 01 September 2019

Temper outbursts in Lowe syndrome: Characteristics, sequence, environmental context and comparison to Prader-Willi syndrome

artículo científico publicado en 2019

The Persistence of Self-injurious and Aggressive Behavior in Males with Fragile X Syndrome Over 8 Years: A Longitudinal Study of Prevalence and Predictive Risk Markers

scientific article published on 01 July 2019

Lista de obras de Hayley Crawford

A Behavioural Assessment of Social Anxiety and Social Motivation in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes

Adaptation of HIV-1 to human leukocyte antigen class I

An experimental study of executive function and social impairment in Cornelia de Lange syndrome.

BDNF Val(66)Met and 5-HTTLPR Genotype are Each Associated with Visual Scanning Patterns of Faces in Young Children

CD8+ T-cell responses to different HIV proteins have discordant associations with viral load

Central role of reverting mutations in HLA associations with human immunodeficiency virus set point

Compensatory mutation partially restores fitness and delays reversion of escape mutation within the immunodominant HLA-B*5703-restricted Gag epitope in chronic human immunodeficiency virus type 1 infection

Control of human immunodeficiency virus type 1 is associated with HLA-B*13 and targeting of multiple gag-specific CD8+ T-cell epitopes

Correction for Thobakgale et al., Impact of HLA in Mother and Child on Disease Progression of Pediatric Human Immunodeficiency Virus Type 1 Infection

Differential effects of anxiety and autism on social scene scanning in males with fragile X syndrome.

Differential selection pressure exerted on HIV by CTL targeting identical epitopes but restricted by distinct HLA alleles from the same HLA supertype

Diverse Profiles of Anxiety Related Disorders in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes

Evolution of HLA-B*5703 HIV-1 escape mutations in HLA-B*5703-positive individuals and their transmission recipients

Face scanning and spontaneous emotion preference in Cornelia de Lange syndrome and Rubinstein-Taybi syndrome.

Fitness cost of escape mutations in p24 Gag in association with control of human immunodeficiency virus type 1

Genetic modifiers in rare disorders: the case of fragile X syndrome

HLA class I-driven evolution of human immunodeficiency virus type 1 subtype c proteome: immune escape and viral load

HLA footprints on human immunodeficiency virus type 1 are associated with interclade polymorphisms and intraclade phylogenetic clustering

Impact of HLA in mother and child on disease progression of pediatric human immunodeficiency virus type 1 infection

Implicit Discrimination of Basic Facial Expressions of Positive/Negative Emotion in Fragile X Syndrome and Autism Spectrum Disorder.

Infant Social Avoidance Predicts Autism but Not Anxiety in Fragile X Syndrome

Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis.

Mutually exclusive T-cell receptor induction and differential susceptibility to human immunodeficiency virus type 1 mutational escape associated with a two-amino-acid difference between HLA class I subtypes

Overactivity, impulsivity and repetitive behaviour in males with fragile X syndrome: contrasting developmental trajectories in those with and without elevated autism symptoms

Proliferative capacity of epitope-specific CD8 T-cell responses is inversely related to viral load in chronic human immunodeficiency virus type 1 infection

Social Avoidance Emerges in Infancy and Persists into Adulthood in Fragile X Syndrome

Temper outbursts in Lowe syndrome: Characteristics, sequence, environmental context and comparison to Prader-Willi syndrome

The Persistence of Self-injurious and Aggressive Behavior in Males with Fragile X Syndrome Over 8 Years: A Longitudinal Study of Prevalence and Predictive Risk Markers

Evolution of HLA-B5703 HIV-1 escape mutations in HLA-B5703-positive individuals and their transmission recipients