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Biochemical and Biophysical Research Communications
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December 17, 2014
Rho-kinase signaling controls nucleocytoplasmic shuttling of class IIa histone deacetylase (HDAC7) and transcriptional activation of orphan nuclear receptor NR4A1
Claudia Compagnucci, Sabina Barresi, Stefania Petrini, et al.
International Journal of Molecular Sciences
|
August 26, 2022
Angioimmunoblastic T-Cell Lymphoma with Exuberant CD30-Positive Follicular Dendritic Cell Proliferation in a SARS-CoV-2 Patient: The Role of Mutational Analysis to Exclude an Associated Follicular Dendritic Cell Sarcoma
Evelina Rogges, Sabrina Pelliccia, Gianluca Lopez, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
June 26, 2024
NTRK3-EML4-rearranged spindle cell tumor with co-expression of S100 and CD34: an unusual mesenchymal tumor in the spectrum of the bland-looking spindle cell lesions of the oral cavity
Giuseppe Broggi, Giulio Attanasio, Antonio Bonanno, et al.
Acta Neuropathologica Communications
|
January 12, 2024
CNS tumor with CREBBP::BCORL1 Fusion and pathogenic mutations in BCOR and CREBBP: expanding the spectrum of BCOR-altered tumors
Valeria Barresi, Antonello Cardoni, Evelina Miele, et al.
Plos One
|
March 19, 2014
Oligophrenin-1 (OPHN1), a gene involved in X-linked intellectual disability, undergoes RNA editing and alternative splicing during human brain development
Sabina Barresi, Sara Tomaselli, Alekos Athanasiadis, et al.
Genes, Chromosomes & Cancer
|
December 11, 2024
Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature
Silvia Vallese, Chantal Tancredi, Isabella Giovannoni, et al.
Stem Cells Translational Medicine
|
May 11, 2016
Rho Kinase Inhibition Is Essential During In Vitro Neurogenesis and Promotes Phenotypic Rescue of Human Induced Pluripotent Stem Cell-Derived Neurons With Oligophrenin-1 Loss of Function
Claudia Compagnucci, Sabina Barresi, Stefania Petrini, et al.
The American Journal of Dermatopathology
|
October 16, 2024
LMNA::NTRK1 and PRDX1::NTRK1 Atypical Spitz Tumor: A Report of Two Additional Cases With Histological, Immunohistochemical, and Molecular Insights
Gerardo Cazzato, Anna Colagrande, Leonardo Resta, et al.
American Journal of Medical Genetics. Part A
|
May 9, 2017
Expanding the phenotypic spectrum of truncating POGZ mutations: Association with CNS malformations, skeletal abnormalities, and distinctive facial dysmorphism
Maria Lisa Dentici, Marcello Niceta, Francesca Pantaleoni, et al.
Clinical Genetics
|
April 5, 2017
Clinical spectrum of Kabuki-like syndrome caused by HNRNPK haploinsufficiency
Maria Lisa Dentici, Sabina Barresi, Marcello Niceta, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 90) with videos related to
Sort By:
Page
of 9
Biochemical and Biophysical Research Communications
|
December 17, 2014
Rho-kinase signaling controls nucleocytoplasmic shuttling of class IIa histone deacetylase (HDAC7) and transcriptional activation of orphan nuclear receptor NR4A1
Claudia Compagnucci, Sabina Barresi, Stefania Petrini, et al.
International Journal of Molecular Sciences
|
August 26, 2022
Angioimmunoblastic T-Cell Lymphoma with Exuberant CD30-Positive Follicular Dendritic Cell Proliferation in a SARS-CoV-2 Patient: The Role of Mutational Analysis to Exclude an Associated Follicular Dendritic Cell Sarcoma
Evelina Rogges, Sabrina Pelliccia, Gianluca Lopez, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
June 26, 2024
NTRK3-EML4-rearranged spindle cell tumor with co-expression of S100 and CD34: an unusual mesenchymal tumor in the spectrum of the bland-looking spindle cell lesions of the oral cavity
Giuseppe Broggi, Giulio Attanasio, Antonio Bonanno, et al.
Acta Neuropathologica Communications
|
January 12, 2024
CNS tumor with CREBBP::BCORL1 Fusion and pathogenic mutations in BCOR and CREBBP: expanding the spectrum of BCOR-altered tumors
Valeria Barresi, Antonello Cardoni, Evelina Miele, et al.
Plos One
|
March 19, 2014
Oligophrenin-1 (OPHN1), a gene involved in X-linked intellectual disability, undergoes RNA editing and alternative splicing during human brain development
Sabina Barresi, Sara Tomaselli, Alekos Athanasiadis, et al.
Genes, Chromosomes & Cancer
|
December 11, 2024
Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature
Silvia Vallese, Chantal Tancredi, Isabella Giovannoni, et al.
Stem Cells Translational Medicine
|
May 11, 2016
Rho Kinase Inhibition Is Essential During In Vitro Neurogenesis and Promotes Phenotypic Rescue of Human Induced Pluripotent Stem Cell-Derived Neurons With Oligophrenin-1 Loss of Function
Claudia Compagnucci, Sabina Barresi, Stefania Petrini, et al.
The American Journal of Dermatopathology
|
October 16, 2024
LMNA::NTRK1 and PRDX1::NTRK1 Atypical Spitz Tumor: A Report of Two Additional Cases With Histological, Immunohistochemical, and Molecular Insights
Gerardo Cazzato, Anna Colagrande, Leonardo Resta, et al.
American Journal of Medical Genetics. Part A
|
May 9, 2017
Expanding the phenotypic spectrum of truncating POGZ mutations: Association with CNS malformations, skeletal abnormalities, and distinctive facial dysmorphism
Maria Lisa Dentici, Marcello Niceta, Francesca Pantaleoni, et al.
Clinical Genetics
|
April 5, 2017
Clinical spectrum of Kabuki-like syndrome caused by HNRNPK haploinsufficiency
Maria Lisa Dentici, Sabina Barresi, Marcello Niceta, et al.
Page
of 9