Lista de obras - Janet Hoenicka - Dominio Público Uruguay

(AAT)n repeat in the cannabinoid receptor gene, CNR1: association with schizophrenia in a Spanish population.

artículo científico publicado en 2006

A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.

artículo científico publicado en 2005

ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism

artículo científico publicado en 2018

An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis.

artículo científico publicado en 1998

Ankyrin Repeat and Kinase Domain Containing 1 Gene, and Addiction Vulnerability

scientific article published on 04 April 2020

Association between cannabinoid receptor gene (CNR1) and childhood attention deficit/hyperactivity disorder in Spanish male alcoholic patients

artículo científico publicado en 2003

Behavioral addictions in early-onset Parkinson disease are associated with DRD3 variants

artículo científico publicado en 2018

C957T DRD2 polymorphism is associated with schizophrenia in Spanish patients

artículo científico publicado en 2006

COMT Val158Met polymorphism and schizophrenia in a series of Spanish patients

artículo científico publicado en 2007

Clinical predictors of response to naltrexone in alcoholic patients: who benefits most from treatment with naltrexone?

artículo científico publicado en 2005

Correction: ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism.

artículo científico publicado en 2018

Dual diagnosis in psychiatric inpatients: prevalence and general characteristics

artículo científico publicado en 2008

Familial focal dystonia

artículo científico publicado en 2002

Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1.

artículo científico publicado en 2005

Human Propionyl-CoA Carboxylase β Subunit Gene: Exon-Intron Definition and Mutation Spectrum in Spanish and Latin American Propionic Acidemia Patients ⬇️

artículo científico publicado el 1 de agosto de 1998

IDRD2 TaqIA polymorphism is associated with urinary homovanillic acid levels in a sample of Spanish male alcoholic patients.

artículo científico publicado en 2004

Impulsivity and sustained attention in pathological gamblers: influence of childhood ADHD history

artículo científico publicado en 2006

Molecular findings in familial Parkinson disease in Spain

scientific article published on 01 June 2002

Motion estimation of subcellular structures from fluorescence microscopy images.

artículo científico publicado en 2017

New frequent mutation in the PCCB gene in Spanish propionic acidemia patients

scientific article published on 01 January 1998

New nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-parkinsonism

scientific article published on 01 March 2001

Performance in the Wisconsin Card Sorting Test and the C957T polymorphism of the DRD2 gene in healthy volunteers

scientific article published on 01 January 2006

Psychopathology and Wisconsin Card Sorting Test performance in male schizophrenic patients: influence of dual diagnosis.

artículo científico publicado en 2007

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

artículo científico publicado en 2014

Sexually dimorphic interaction between the DRD1 and COMT genes in schizophrenia.

artículo científico publicado en 2010

Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein.

artículo científico publicado en 2002

Targeting, endocytosis, and lysosomal delivery of active enzymes to model human neurons by ICAM-1-targeted nanocarriers.

artículo científico publicado en 2014

The ANKK1 gene associated with addictions is expressed in astroglial cells and upregulated by apomorphine.

artículo científico publicado en 2010

The ANKK1 kinase gene and psychiatric disorders.

artículo científico publicado en 2009

The ANKK1/DRD2 locus is a genomic substrate for affective priming and recognition of angry faces.

artículo científico publicado en 2015

The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R- and D2R-Like Dopamine Receptors.

artículo científico publicado en 2015

The Addiction-Related Protein ANKK1 is Differentially Expressed During the Cell Cycle in Neural Precursors.

artículo científico publicado en 2016

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

scientific article published on 29 October 2019

The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases

artículo científico publicado en 2021

The SCR1 gene from Schwanniomyces occidentalis encodes a highly hydrophobic polypeptide, which confers ribosomal resistance to cycloheximide.

artículo científico publicado en 2002

The TaqIA polymorphism linked to the DRD2 gene is related to lower attention and less inhibitory control in alcoholic patients.

artículo científico publicado en 2005

The addiction-related gene ANKK1 in Parkinsonian patients with impulse control disorder.

artículo científico publicado en 2014

The anti-inflammatory prostaglandin 15d-PGJ2 and its nuclear receptor PPARgamma are decreased in schizophrenia

scientific article published on 18 February 2011

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia

artículo científico publicado en 2004

The tau gene A0 allele and progressive supranuclear palsy.

artículo científico publicado en 1999

Two different genes from Schwanniomyces occidentalis determine ribosomal resistance to cycloheximide.

artículo científico publicado en 1993

Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 families

artículo científico publicado en 2003

[CADASIL: a case with clinical, radiological, histological and genetic diagnoses]

artículo científico publicado en 2003

Lista de obras de Janet Hoenicka

(AAT)n repeat in the cannabinoid receptor gene, CNR1: association with schizophrenia in a Spanish population.

A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.

ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism

An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis.

Ankyrin Repeat and Kinase Domain Containing 1 Gene, and Addiction Vulnerability

Association between cannabinoid receptor gene (CNR1) and childhood attention deficit/hyperactivity disorder in Spanish male alcoholic patients

Behavioral addictions in early-onset Parkinson disease are associated with DRD3 variants

C957T DRD2 polymorphism is associated with schizophrenia in Spanish patients

COMT Val158Met polymorphism and schizophrenia in a series of Spanish patients

Clinical predictors of response to naltrexone in alcoholic patients: who benefits most from treatment with naltrexone?

Correction: ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism.

Dual diagnosis in psychiatric inpatients: prevalence and general characteristics

Familial focal dystonia

Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1.

Human Propionyl-CoA Carboxylase β Subunit Gene: Exon-Intron Definition and Mutation Spectrum in Spanish and Latin American Propionic Acidemia Patients ⬇️

IDRD2 TaqIA polymorphism is associated with urinary homovanillic acid levels in a sample of Spanish male alcoholic patients.

Impulsivity and sustained attention in pathological gamblers: influence of childhood ADHD history

Molecular findings in familial Parkinson disease in Spain

Motion estimation of subcellular structures from fluorescence microscopy images.

New frequent mutation in the PCCB gene in Spanish propionic acidemia patients

New nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-parkinsonism

Performance in the Wisconsin Card Sorting Test and the C957T polymorphism of the DRD2 gene in healthy volunteers

Psychopathology and Wisconsin Card Sorting Test performance in male schizophrenic patients: influence of dual diagnosis.

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

Sexually dimorphic interaction between the DRD1 and COMT genes in schizophrenia.

Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein.

Targeting, endocytosis, and lysosomal delivery of active enzymes to model human neurons by ICAM-1-targeted nanocarriers.

The ANKK1 gene associated with addictions is expressed in astroglial cells and upregulated by apomorphine.

The ANKK1 kinase gene and psychiatric disorders.

The ANKK1/DRD2 locus is a genomic substrate for affective priming and recognition of angry faces.

The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R- and D2R-Like Dopamine Receptors.

The Addiction-Related Protein ANKK1 is Differentially Expressed During the Cell Cycle in Neural Precursors.

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases

The SCR1 gene from Schwanniomyces occidentalis encodes a highly hydrophobic polypeptide, which confers ribosomal resistance to cycloheximide.

The TaqIA polymorphism linked to the DRD2 gene is related to lower attention and less inhibitory control in alcoholic patients.

The addiction-related gene ANKK1 in Parkinsonian patients with impulse control disorder.

The anti-inflammatory prostaglandin 15d-PGJ2 and its nuclear receptor PPARgamma are decreased in schizophrenia

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia

The tau gene A0 allele and progressive supranuclear palsy.

Two different genes from Schwanniomyces occidentalis determine ribosomal resistance to cycloheximide.

Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 families

[CADASIL: a case with clinical, radiological, histological and genetic diagnoses]