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Genomewide miRNA profiling of oral lichenoid disorders and oral squamous cell carcinoma

Oral diseases, 2016-11, Vol.22 (8), p.754-760

2016

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Genetic characterization and founder effect analysis of recently introduced Salers cattle breed population

Animal (Cambridge, England), 2017-01, Vol.11 (1), p.24-32

2017

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Phenotypic variability in familial prion diseases due to the D178N mutation

Journal of neurology, neurosurgery and psychiatry, 2005-11, Vol.76 (11), p.1491-1496

2005

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A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

Neurology, 2005-05, Vol.64 (9), p.1578-1585

2005

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Global DNA methylation: uncommon event in oral lichenoid disease

Oral diseases, 2014-11, Vol.20 (8), p.821-826

2014

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Gene promoter hypermethylation in oral rinses of leukoplakia patients—a diagnostic and/or prognostic tool?

European journal of cancer (1990), 2003-11, Vol.39 (16), p.2306-2309

2003

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Genomewide mi RNA profiling of oral lichenoid disorders and oral squamous cell carcinoma

Oral diseases, 2016-11, Vol.22 (8), p.754-760

2016

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Progression from amnesic mild cognitive impairment to Alzheimer's disease: ESR1 and ESR2 polymorphisms and APOE gene

Dementia and geriatric cognitive disorders, 2011-01, Vol.32 (5), p.332-341

2011

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Frequent loss of p53 codon 72 Pro variant in hepatitis C virus-positive carriers with hepatocellular carcinoma

Cancer letters, 2003-04, Vol.193 (2), p.199-205

2003

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Microsatellites and Alu elements from the human MHC in Valencia (Spain): analysis of genetic relationships and linkage disequilibrium

International journal of immunogenetics, 2011-12, Vol.38 (6), p.483-491

2011

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X-linked microsatellites in two Northern Spain populations

Forensic science international, 2004-10, Vol.145 (1), p.57-59

2004

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The Basques according to polymorphic Alu insertions

Human genetics, 2001-08, Vol.109 (2), p.224-233

2001

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Microsatellite data support subpopulation structuring among Basques

Journal of human genetics, 2005-09, Vol.50 (8), p.403-414

2005

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Population Genetics and Forensic Applications Using Multiplex PCR (CSF1PO, TPOX, and TH01) Loci in the Basque Country

Journal of forensic sciences, 1998-11, Vol.43 (6), p.1181-1187

1998

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Allelic frequencies of 13 STR loci in autochthonous Basques from the province of Vizcaya (Spain)

Forensic science international, 2005-09, Vol.152 (2), p.259-262

2005

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Study of six X-linked tetranucleotide microsatellites: population data from five Spanish regions

International journal of legal medicine, 2006-05, Vol.120 (3), p.147-150

2006

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Genetic variability in autochthonous Basques from Guipuzcoa: a view from MHC microsatellites

International journal of immunogenetics, 2010-08, Vol.37 (4), p.279-287

2010

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Sequence structure and population data of two X-linked markers: DXS7423 and DXS8377

International journal of legal medicine, 2002-12, Vol.116 (6), p.368-371

2002

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Use of cytological specimens for p53 gene alteration detection in oral squamous cell carcinoma risk patients

Clinical oncology (Royal College of Radiologists (Great Britain)), 2004-08, Vol.16 (5), p.366-370

2004

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Patterns of methylation profiles as diagnostic markers for multiple hepatocellular carcinomas

Scandinavian journal of gastroenterology, 2004, Vol.39 (3), p.246-251

2004

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Ancestral origins of the prion protein gene D178N mutation in the Basque Country

Human genetics, 2005-06, Vol.117 (1), p.61-69

2005

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5-Hydroxytryptamine 6 receptor (5-HT 6) receptor and apolipoprotein E (ApoE) polymorphisms in patients with Alzheimer's disease in the Basque Country

Neuroscience letters, 2003-03, Vol.339 (1), p.85-87

2003

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No association between GSTP1 gene aberrant promoter methylation and prognosis in surgically resected hepatocellular carcinoma patients from the Basque Country (Northern Spain)

Liver international, 2003-08, Vol.23 (4), p.249-254

2003

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Genetic polymorphisms at 13 STR loci in autochthonous Basques from the province of Alava (Spain)

Legal medicine (Tokyo, Japan), 2005, Vol.7 (1), p.58-61

2005

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Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework

Forensic science international, 2003-03, Vol.132 (1), p.82-83

2003

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Genomewide miRNA profiling of oral lichenoid disorders and oral squamous cell carcinoma

Genetic characterization and founder effect analysis of recently introduced Salers cattle breed population

Phenotypic variability in familial prion diseases due to the D178N mutation

A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

Global DNA methylation: uncommon event in oral lichenoid disease

Gene promoter hypermethylation in oral rinses of leukoplakia patients—a diagnostic and/or prognostic tool?

Genomewide mi RNA profiling of oral lichenoid disorders and oral squamous cell carcinoma

Progression from amnesic mild cognitive impairment to Alzheimer's disease: ESR1 and ESR2 polymorphisms and APOE gene

Frequent loss of p53 codon 72 Pro variant in hepatitis C virus-positive carriers with hepatocellular carcinoma

Microsatellites and Alu elements from the human MHC in Valencia (Spain): analysis of genetic relationships and linkage disequilibrium

X-linked microsatellites in two Northern Spain populations

The Basques according to polymorphic Alu insertions

Microsatellite data support subpopulation structuring among Basques

Population Genetics and Forensic Applications Using Multiplex PCR (CSF1PO, TPOX, and TH01) Loci in the Basque Country

Allelic frequencies of 13 STR loci in autochthonous Basques from the province of Vizcaya (Spain)

Study of six X-linked tetranucleotide microsatellites: population data from five Spanish regions

Genetic variability in autochthonous Basques from Guipuzcoa: a view from MHC microsatellites

Sequence structure and population data of two X-linked markers: DXS7423 and DXS8377

Use of cytological specimens for p53 gene alteration detection in oral squamous cell carcinoma risk patients

Patterns of methylation profiles as diagnostic markers for multiple hepatocellular carcinomas

Ancestral origins of the prion protein gene D178N mutation in the Basque Country

5-Hydroxytryptamine 6 receptor (5-HT 6) receptor and apolipoprotein E (ApoE) polymorphisms in patients with Alzheimer's disease in the Basque Country

No association between GSTP1 gene aberrant promoter methylation and prognosis in surgically resected hepatocellular carcinoma patients from the Basque Country (Northern Spain)

Genetic polymorphisms at 13 STR loci in autochthonous Basques from the province of Alava (Spain)

Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework

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