Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprintedL3MBTL1gene-Reference-Cited by-同舟云学术

Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprintedL3MBTL1gene

Published:2016-09-21 Issue:1 Volume:56 Page:51-58
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Nacci Lucia¹,Valli Roberto²,Maria Pinto Rita³,Zecca Marco⁴,Cipolli Marco⁵,Morini Jacopo⁶,Cesaro Simone⁷,Boveri Emanuela⁸,Rosti Vittorio⁹,Corti Paola¹⁰,Ambroni Maura¹¹,Pasquali Francesco²,Danesino Cesare¹,Maserati Emanuela²,Minelli Antonella¹

Affiliation:

1. Department of Molecular Medicine; University of Pavia; Pavia Italy

2. Department of Clinical and Experimental Medicine; University of Insubria; Varese Italy

3. Ospedale Bambino Gesù IRCCS; Oncoematologia e Medicina Trasfusionale; Roma Italy

4. Oncoematologia Pediatrica, Fondazione IRCCS Policlinico San Matteo; Pavia Italy

5. Cystic Fibrosis Centre, Azienda Ospedaliera Universitaria; Verona Italy

6. Department of Physics; University of Pavia; Italy

7. Oncoematologia Pediatrica, Azienda Ospedaliera Universitaria Integrata; Verona Italy

8. Fondazione IRCCS Policlinico; Anatomic Pathology Section; San Matteo, Pavia Italy

9. IRCCS Policlinico San Matteo; Center for the Study of Myelofibrosis, Biotechnology Research Area; Pavia Italy

10. Pediatrics Unit, Fondazione Medico e Brianza per il Bambino e la sua Mamma; Monza Italy

11. Cystic Fibrosis Regional Center, Ospedale M. Bufalini; Cesena Italy

Publisher

Wiley

Subject

Cancer Research,Genetics

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4. Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies;Bench;Br J Haematol,2004

5. The human L(3)MBT polycomb group protein is a transcriptional repressor and interacts physically and functionally with TEL (ETV6);Boccuni;J Biol Chem,2003

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4. Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor;Frontiers in Immunology;2022-06-24

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