List of works - Rebeca Martínez-Hernández

A microRNA signature for evaluation of risk and severity of Autoimmune Thyroid Diseases.

scientific article published on 9 January 2018

Abnormalities in early markers of muscle involvement support a delay in myogenesis in spinal muscular atrophy.

scientific article published in June 2014

Accuracy of marker analysis, quantitative real-time polymerase chain reaction, and multiple ligation-dependent probe amplification to determine SMN2 copy number in patients with spinal muscular atrophy.

scientific article published on 6 May 2011

Analysis of expression of the PD-1/PD-L1 immune checkpoint system and its prognostic impact in gastroenteropancreatic neuroendocrine tumors

scientific article published in Scientific Reports

Analysis of the C9orf72 gene in spinal muscular atrophy patients.

scientific article published on 7 July 2014

Circulating Microvesicles Regulate Treg and Th17 Differentiation in Human Autoimmune Thyroid Disorders.

scientific article

Decay in survival motor neuron and plastin 3 levels during differentiation of iPSC-derived human motor neurons.

scientific article

Evaluation of fetal nuchal translucency in 98 pregnancies at risk for severe spinal muscular atrophy: possible relevance of the SMN2 copy number ⬇️

scientific article published on November 30, 2011

Expression and Function of the Costimulatory Receptor SLAMF1 Is Altered in Lymphocytes From Patients With Autoimmune Thyroiditis

scientific article published on 17 November 2016

Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene.

scientific article

Integrated miRNA and mRNA expression profiling identifies novel targets and pathological mechanisms in autoimmune thyroid diseases

scientific article published on 14 November 2019

LAT-1 and GLUT-1 Carrier Expression and Its Prognostic Value in Gastroenteropancreatic Neuroendocrine Tumors

scientific article published on 13 October 2020

Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene.

scientific article published on 3 December 2008

Pathogenic Th17 and Th22 cells are increased in patients with autoimmune thyroid disorders

scientific article published on 01 July 2017

Patients With Autoimmune Thyroiditis Show Diminished Levels and Defective Suppressive Function of Tr1 Regulatory Lymphocytes

scientific article published on 01 September 2018

Response to Letter to the Editor: "Patients With Autoimmune Thyroiditis Show Diminished Levels and Defective Suppressive Function of Tr1 Regulatory Lymphocytes"

scientific article published on 01 January 2020

The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

scientific article published on 24 June 2010

The developmental pattern of myotubes in spinal muscular atrophy indicates prenatal delay of muscle maturation.

scientific article published in May 2009

Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability.

scientific article

Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy

scientific article published on 30 December 2010

List of works by Rebeca Martínez-Hernández

A microRNA signature for evaluation of risk and severity of Autoimmune Thyroid Diseases.

Abnormalities in early markers of muscle involvement support a delay in myogenesis in spinal muscular atrophy.

Accuracy of marker analysis, quantitative real-time polymerase chain reaction, and multiple ligation-dependent probe amplification to determine SMN2 copy number in patients with spinal muscular atrophy.

Analysis of expression of the PD-1/PD-L1 immune checkpoint system and its prognostic impact in gastroenteropancreatic neuroendocrine tumors

Analysis of the C9orf72 gene in spinal muscular atrophy patients.

Circulating Microvesicles Regulate Treg and Th17 Differentiation in Human Autoimmune Thyroid Disorders.

Decay in survival motor neuron and plastin 3 levels during differentiation of iPSC-derived human motor neurons.

Evaluation of fetal nuchal translucency in 98 pregnancies at risk for severe spinal muscular atrophy: possible relevance of the SMN2 copy number ⬇️

Expression and Function of the Costimulatory Receptor SLAMF1 Is Altered in Lymphocytes From Patients With Autoimmune Thyroiditis

Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene.

Integrated miRNA and mRNA expression profiling identifies novel targets and pathological mechanisms in autoimmune thyroid diseases

LAT-1 and GLUT-1 Carrier Expression and Its Prognostic Value in Gastroenteropancreatic Neuroendocrine Tumors

Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene.

Pathogenic Th17 and Th22 cells are increased in patients with autoimmune thyroid disorders

Patients With Autoimmune Thyroiditis Show Diminished Levels and Defective Suppressive Function of Tr1 Regulatory Lymphocytes

Response to Letter to the Editor: "Patients With Autoimmune Thyroiditis Show Diminished Levels and Defective Suppressive Function of Tr1 Regulatory Lymphocytes"

The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

The developmental pattern of myotubes in spinal muscular atrophy indicates prenatal delay of muscle maturation.

Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability.

Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy