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Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks

BMC genomics, 2014-07, Vol.15 (1), p.624-624

2014

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Detection of BRAF mutations in patients with hairy cell leukemia and related lymphoproliferative disorders

Haematologica (Roma), 2012-05, Vol.97 (5), p.780-783

2012

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A multisite blinded study for the detection of BRAF mutations in formalin-fixed, paraffin-embedded malignant melanoma

Scientific reports, 2013-04, Vol.3 (1), p.1659-1659, Article 1659

2013

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Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome

PloS one, 2010-07, Vol.5 (7), p.e11561-e11561

2010

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Hematopoietic defects in the Ts1Cje mouse model of Down syndrome

Blood, 2009-02, Vol.113 (9), p.1929-1937

2009

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Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis

Cerebral cortex (New York, N.Y. 1991), 2011-03, Vol.21 (3), p.683-697

2011

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Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndrome

PloS one, 2011-02, Vol.6 (2), p.e16831-e16831

2011

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ROS1 rearrangements in non-small cell lung cancer: screening by immunohistochemistry using proportion of cells staining without intensity and excluding cases with MAPK pathway drivers improves test performance

Pathology, 2022-04, Vol.54 (3), p.279-285

2022

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Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome

Genomics data, 2014-12, Vol.2 (C), p.314-317

2014

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Gene and protein expression profiles of JAK-STAT signalling pathway in the developing brain of the Ts1Cje down syndrome mouse model

International journal of neuroscience, 2019-09, Vol.129 (9), p.871-881

2019

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Proteomic and Metabolomic Analyses of Mitochondrial Complex I-deficient Mouse Model Generated by Spontaneous B2 Short Interspersed Nuclear Element (SINE) Insertion into NADH Dehydrogenase (Ubiquinone) Fe-S Protein 4 (Ndufs4) Gene

The Journal of biological chemistry, 2012-06, Vol.287 (24), p.20652-20663

2012

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Expression Profiling of Notch Signalling Pathway and Gamma-Secretase Activity in the Brain of Ts1Cje Mouse Model of Down Syndrome

Journal of molecular neuroscience, 2019-04, Vol.67 (4), p.632-642

2019

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Identification of a recurrent mosaic KRAS variant in brain tissue from an individual with nevus sebaceous syndrome

Cold Spring Harbor molecular case studies, 2021-12, Vol.7 (6), p.a006133

2021

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Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2 V617F mutant allele detection

BMC cancer, 2013-04, Vol.13 (1), p.206-206

2013

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Molecular networks involved in mouse cerebral corticogenesis and spatio-temporal regulation of Sox4 and Sox11 novel antisense transcripts revealed by transcriptome profiling

Genome biology, 2009-01, Vol.10 (10), p.R104-R104

2009

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1.29 Development of Highly Accurate RT-qPCR Assays for Profiling the Expression of DNA Repair and Apoptosis Genes in CLL

Clinical lymphoma, myeloma and leukemia, 2011-10, Vol.11, p.S158-S159

2011

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Analysing DNA methylation using bisulphite pyrosequencing

Methods in molecular biology (Clifton, N.J.), 2011, Vol.791, p.33

2011

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1.30 Caspase 10 is Down-Regulated in Chronic Lymphocytic Leukemia

Clinical lymphoma, myeloma and leukemia, 2011-10, Vol.11, p.S159-S159

2011

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T1715 The Role of Genetic and Epigenetic Variation of DNA Methyltransferases in Hyperplastic Polyposis Syndrome

Gastroenterology (New York, N.Y. 1943), 2010, Vol.138 (5), p.S-563-S-563

2010

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Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2V617F mutant allele detection

BMC cancer, 2013-04, Vol.13 (1), Article 206

2013

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Hematopoietic defects in the TslCje mouse model of Down syndrome

Blood, 2009, Vol.113 (9), p.1929-1937

2009

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Breast ductal carcinoma in situ carry mutational driver events representative of invasive breast cancer

Modern pathology, 2017-07, Vol.30 (7), p.952-963

2017

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The impact of molecular and mismatch repair status on the survival outcomes of surgically treated patients with colorectal peritoneal metastases

European journal of surgical oncology, 2022-10, Vol.48 (10), p.2218-2225

2022

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Towards Routine Implementation of Liquid Biopsies in Cancer Management: It Is Always Too Early, until Suddenly It Is Too Late

Diagnostics (Basel), 2021-01, Vol.11 (1), p.103

2021

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High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort

PloS one, 2013-07, Vol.8 (7), p.e69026-e69026

2013

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Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks

Detection of BRAF mutations in patients with hairy cell leukemia and related lymphoproliferative disorders

A multisite blinded study for the detection of BRAF mutations in formalin-fixed, paraffin-embedded malignant melanoma

Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome

Hematopoietic defects in the Ts1Cje mouse model of Down syndrome

Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis

Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndrome

ROS1 rearrangements in non-small cell lung cancer: screening by immunohistochemistry using proportion of cells staining without intensity and excluding cases with MAPK pathway drivers improves test performance

Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome

Gene and protein expression profiles of JAK-STAT signalling pathway in the developing brain of the Ts1Cje down syndrome mouse model

Proteomic and Metabolomic Analyses of Mitochondrial Complex I-deficient Mouse Model Generated by Spontaneous B2 Short Interspersed Nuclear Element (SINE) Insertion into NADH Dehydrogenase (Ubiquinone) Fe-S Protein 4 (Ndufs4) Gene

Expression Profiling of Notch Signalling Pathway and Gamma-Secretase Activity in the Brain of Ts1Cje Mouse Model of Down Syndrome

Identification of a recurrent mosaic KRAS variant in brain tissue from an individual with nevus sebaceous syndrome

Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2 V617F mutant allele detection

Molecular networks involved in mouse cerebral corticogenesis and spatio-temporal regulation of Sox4 and Sox11 novel antisense transcripts revealed by transcriptome profiling

1.29 Development of Highly Accurate RT-qPCR Assays for Profiling the Expression of DNA Repair and Apoptosis Genes in CLL

Analysing DNA methylation using bisulphite pyrosequencing

1.30 Caspase 10 is Down-Regulated in Chronic Lymphocytic Leukemia

T1715 The Role of Genetic and Epigenetic Variation of DNA Methyltransferases in Hyperplastic Polyposis Syndrome

Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2V617F mutant allele detection

Hematopoietic defects in the TslCje mouse model of Down syndrome

Breast ductal carcinoma in situ carry mutational driver events representative of invasive breast cancer

The impact of molecular and mismatch repair status on the survival outcomes of surgically treated patients with colorectal peritoneal metastases

Towards Routine Implementation of Liquid Biopsies in Cancer Management: It Is Always Too Early, until Suddenly It Is Too Late

High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort

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