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Expression of epigenetic pathway related genes in association with PD-L1, ER/PgR and MLH1 in endometrial carcinoma

PloS one, 2022-02, Vol.17 (2), p.e0264014

2022

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Relapsed NPM1 mutated acute myeloid leukemia with PDGFRA rearrangement

Blood, 2019-01, Vol.133 (2), p.181-181

2019

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Profiling and functional analyses of microRNAs and their target gene products in human uterine leiomyomas

PloS one, 2010-08, Vol.5 (8), p.e12362-e12362

2010

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Immunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case study

Journal of neuroinflammation, 2012-01, Vol.9 (1), p.4-4, Article 4

2012

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Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events

Leukemia research, 2018-10, Vol.73, p.86-94

2018

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Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes

Journal of neuroimmunology, 2011-09, Vol.238 (1), p.73-80

2011

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iAMP21 in acute myeloid leukemia is associated with complex karyotype, TP53 mutation and dismal outcome

Modern pathology, 2020-07, Vol.33 (7), p.1389-1397

2020

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Molecular and immunohistochemical evidence for the origin of uterine leiomyosarcomas from associated leiomyoma and symplastic leiomyoma-like areas

Modern pathology, 2009-10, Vol.22 (10), p.1303-1311

2009

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Clonal cytogenetic abnormalities in donor-derived cells after sex mismatched allogeneic stem cell transplantation

Cancer genetics, 2021-11, Vol.258-259, p.120-130

2021

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LPL deletion is associated with poorer response to ibrutinib-based treatments and overall survival in TP53-deleted chronic lymphocytic leukemia

Annals of hematology, 2020-10, Vol.99 (10), p.2343-2349

2020

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AKT, EGFR, C-ErbB-2, and C-kit expression in uterine carcinosarcoma

International journal of gynecological pathology, 2013-09, Vol.32 (5), p.493

2013

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Deciphering the complexities of MECOM rearrangement-driven chromosomal aberrations

Cancer genetics, 2019-04, Vol.233-234, p.21-31

2019

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Matricellular protein CCN1 ( CYR61 ) expression is associated with high-grade ductal carcinoma in situ

Human pathology, 2014-06, Vol.45 (6), p.1269-1275

2014

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Is hyperdiploidy a favorable cytogenetics in adults with B‐lymphoblastic leukemia?

Cancer medicine (Malden, MA), 2019-08, Vol.8 (9), p.4093-4099

2019

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HOXA4 Gene Promoter Hypermethylation as an Epigenetic Mechanism Mediating Resistance to Imatinib Mesylate in Chronic Myeloid Leukemia Patients

BioMed research international, 2013-01, Vol.2013, p.129715-7

2013

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IROme, a New High-Throughput Molecular Tool for the Diagnosis of Inherited Retinal Dystrophies

BioMed research international, 2013-01, Vol.2013, p.198089-9

2013

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Experience of Preimplantation Genetic Diagnosis with HLA Matching at the University Hospital Virgen del Rocío in Spain: Technical and Clinical Overview

BioMed research international, 2014-01, Vol.2014, p.560160-8

2014

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Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity

European journal of human genetics : EJHG, 2006-06, Vol.14 (6), p.791-797

2006

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Detection of C. trachomatis in the Serum of the Patients with Urogenital Chlamydiosis

BioMed research international, 2013-01, Vol.2013, p.489489-7

2013

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An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation

American journal of medical genetics. Part A, 2007-04, Vol.143A (8), p.824-829

2007

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MET Amplification (MET/CEP7 Ratio ≥ 1.8) Is an Independent Poor Prognostic Marker in Patients With Treatment-naive Non–Small-cell Lung Cancer

Clinical lung cancer, 2021-07, Vol.22 (4), p.e512-e518

2021

Volltextzugriff (PDF)

Acquired MET amplification in non-small cell lung cancer is highly associated with the exposure of EGFR inhibitors and may not affect patients' outcome

Experimental and molecular pathology, 2021-02, Vol.118, p.104572, Article 104572

2021

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Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature

Clinical dysmorphology, 2007-07, Vol.16 (3), p.135

2007

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Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

Genetics in medicine, 2010-02, Vol.12 (2), p.85-92

2010

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Expression profiling reveals MSX1 and EphB2 expression correlates with the invasion capacity of Wilms tumors

Pediatric blood & cancer, 2011-12, Vol.57 (6), p.950-957

2011

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Expression of epigenetic pathway related genes in association with PD-L1, ER/PgR and MLH1 in endometrial carcinoma

Relapsed NPM1 mutated acute myeloid leukemia with PDGFRA rearrangement

Profiling and functional analyses of microRNAs and their target gene products in human uterine leiomyomas

Immunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case study

Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events

Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes

iAMP21 in acute myeloid leukemia is associated with complex karyotype, TP53 mutation and dismal outcome

Molecular and immunohistochemical evidence for the origin of uterine leiomyosarcomas from associated leiomyoma and symplastic leiomyoma-like areas

Clonal cytogenetic abnormalities in donor-derived cells after sex mismatched allogeneic stem cell transplantation

LPL deletion is associated with poorer response to ibrutinib-based treatments and overall survival in TP53-deleted chronic lymphocytic leukemia

AKT, EGFR, C-ErbB-2, and C-kit expression in uterine carcinosarcoma

Deciphering the complexities of MECOM rearrangement-driven chromosomal aberrations

Matricellular protein CCN1 ( CYR61 ) expression is associated with high-grade ductal carcinoma in situ

Is hyperdiploidy a favorable cytogenetics in adults with B‐lymphoblastic leukemia?

HOXA4 Gene Promoter Hypermethylation as an Epigenetic Mechanism Mediating Resistance to Imatinib Mesylate in Chronic Myeloid Leukemia Patients

IROme, a New High-Throughput Molecular Tool for the Diagnosis of Inherited Retinal Dystrophies

Experience of Preimplantation Genetic Diagnosis with HLA Matching at the University Hospital Virgen del Rocío in Spain: Technical and Clinical Overview

Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity

Detection of C. trachomatis in the Serum of the Patients with Urogenital Chlamydiosis

An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation

MET Amplification (MET/CEP7 Ratio ≥ 1.8) Is an Independent Poor Prognostic Marker in Patients With Treatment-naive Non–Small-cell Lung Cancer

Acquired MET amplification in non-small cell lung cancer is highly associated with the exposure of EGFR inhibitors and may not affect patients' outcome

Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

Expression profiling reveals MSX1 and EphB2 expression correlates with the invasion capacity of Wilms tumors

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