Francesco Acquadro
Overview
Explore the profile of Francesco Acquadro including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
315
Followers
0
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Recent Articles
1.
Riveiro-Falkenbach E, Ruano Y, Garcia-Martin R, Lora D, Cifdaloz M, Acquadro F, et al.
Pigment Cell Melanoma Res
. 2016 Nov;
30(2):194-202.
PMID: 27893188
DEK is an oncoprotein involved in a variety of cellular functions, such as DNA repair, replication, and transcriptional control. DEK is preferentially expressed in actively proliferating and malignant cells, including...
2.
Bigagli E, De Filippo C, Castagnini C, Toti S, Acquadro F, Giudici F, et al.
Cell Oncol (Dordr)
. 2016 Oct;
39(6):545-558.
PMID: 27709558
Background: DNA copy number alterations (CNAs) and gene expression changes have amply been encountered in colorectal cancers (CRCs), but the extent at which CNAs affect gene expression, as well as...
3.
Santos-Briz A, Riveiro-Falkenbach E, Roman-Curto C, Mir-Bonafe J, Acquadro F, Mentzel T
Am J Dermatopathol
. 2014 Jul;
36(11):920-4.
PMID: 25072679
Dermatofibrosarcoma protuberans (DFSP) is a dermal and subcutaneous slow-growing tumor of intermediate malignancy. Different histological variants of DFSP have been described, depending on cellular and stromal peculiarities. Here, we report...
4.
Salgado R, Menezes J, Calvente M, Suela J, Acquadro F, Martinez-Laperche C, et al.
Leuk Lymphoma
. 2014 Mar;
55(11):2652-5.
PMID: 24635575
No abstract available.
5.
Hafner C, Toll A, Gantner S, Mauerer A, Lurkin I, Acquadro F, et al.
J Med Genet
. 2012 Apr;
49(4):249-53.
PMID: 22499344
Background: Activating RAS mutations in the germline cause rare developmental disorders such as Costello syndrome. Somatic RAS mutations are found in approximately 30% of human cancers. Keratinocytic epidermal nevi (KEN)...
6.
Rio-Machin A, Menezes J, Maiques-Diaz A, Agirre X, Ferreira B, Acquadro F, et al.
Haematologica
. 2011 Nov;
97(4):534-7.
PMID: 22102704
The disruption of RUNX1 function is one of the main mechanisms of disease observed in hematopoietic malignancies and the description of novel genetic events that lead to a RUNX1 loss...
7.
Tejada M, Martinez-Bouzas C, Garcia-Ribes A, Larrucea S, Acquadro F, Cigudosa J, et al.
Pediatrics
. 2011 Sep;
128(4):e1029-33.
PMID: 21930553
Multiplex ligation-dependent probe amplification (MLPA) and array- comparative genomic hybridization analysis have been proven to be useful in the identification of submicroscopic copy-number imbalances in families with nonsyndromic X-linked intellectual...
8.
Menezes J, Acquadro F, Perez-Pons de la Villa C, Garcia-Sanchez F, Alvarez S, Cigudosa J
Haematologica
. 2011 Jul;
96(10):1565-6.
PMID: 21750086
No abstract available.
9.
Hafner C, Toll A, Fernandez-Casado A, Earl J, Marques M, Acquadro F, et al.
Proc Natl Acad Sci U S A
. 2010 Nov;
107(48):20780-5.
PMID: 21078999
Malignant tumors result from the accumulation of genetic alterations in oncogenes and tumor suppressor genes. Much less is known about the genetic changes in benign tumors. Seborrheic keratoses (SK) are...
10.
Sbacchi S, Acquadro F, Calo I, Cali F, Romano V
Curr Genomics
. 2010 Oct;
11(2):136-45.
PMID: 20885821
We have used Gene Ontology (GO) and pathway analyses to uncover the common functions associated to the genes overlapping Copy Number Variants (CNVs) in autistic patients. Our source of data...