Search Results - "D'Urso, Michele"
-
1
Clinical diagnosis of incontinentia pigmenti in a cohort of male patients
Published in Journal of the American Academy of Dermatology (01-02-2007)“…Eighteen male patients with incontinentia pigmenti (IP) showed the characteristic clinical features and, when examined, histologic skin defects observed in…”
Get full text
Journal Article -
2
Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations
Published in Human mutation (01-05-2008)“…Mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG), also called nuclear factor-kappaB (NF-kB) essential…”
Get full text
Journal Article -
3
An Effective Hybrid Approach for the Optimal Synthesis of Monopulse Antennas
Published in IEEE transactions on antennas and propagation (01-04-2007)“…The problem of synthesizing "optimal" sum and difference patterns subject to arbitrary sidelobe bounds by means of a simple feeding network is dealt with. It…”
Get full text
Journal Article -
4
Effective Solution of 3-D Scattering Problems via Series Expansions: Applicability and a New Hybrid Scheme
Published in IEEE transactions on geoscience and remote sensing (01-03-2007)“…Accurate and reliable evaluation of the electromagnetic field scattered by dielectric objects is a canonical problem in the electromagnetic community. In the…”
Get full text
Journal Article -
5
Inverse Profiling via an Effective Linearized Scattering Model and MRF Regularization
Published in IEEE geoscience and remote sensing letters (01-11-2011)“…The aim of this letter is to show how a joint adoption of a suitable regularization scheme and a proper rewriting of the traditional electromagnetic scattering…”
Get full text
Journal Article -
6
Longins: a new evolutionary conserved VAMP family sharing a novel SNARE domain
Published in Trends in biochemical sciences (Amsterdam. Regular ed.) (01-07-2001)“…This article describes the discovery of a novel SNARE domain that might be involved in the regulation of membrane fusion. This domain is shared by a novel…”
Get full text
Journal Article -
7
Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with incontinentia pigmenti
Published in Human mutation (01-09-2009)“…The Incontinentia Pigmenti (IP) locus contains the IKBKG/NEMO/IKKgamma gene and its truncated pseudogene copy, IKBKGP/deltaNEMO. The major genetic defect in IP…”
Get full text
Journal Article -
8
Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2–q28 associated with ovarian dysfunction
Published in Human reproduction (Oxford) (01-02-2006)“…BACKGROUND: Deletions of Xq chromosome are reported for a number of familial conditions exhibiting premature ovarian failure (POF) and early menopause (EM)…”
Get full text
Journal Article -
9
DDX11L: a novel transcript family emerging from human subtelomeric regions
Published in BMC genomics (28-05-2009)“…The subtelomeric regions of human chromosomes exhibit an extraordinary plasticity. To date, due to the high GC content and to the presence of telomeric…”
Get full text
Journal Article -
10
Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]
Published in Brain & development (Tokyo. 1979) (01-11-2012)Get full text
Journal Article -
11
Maximally Sparse, Steerable, and Nonsuperdirective Array Antennas via Convex Optimizations
Published in IEEE transactions on antennas and propagation (01-09-2016)“…Achieving the minimum number of radiating elements in the active electronically scanned array synthesis represents a key problem in those applications where…”
Get full text
Journal Article -
12
Characterization of the human STAT5A and STAT5B promoters: evidence of a positive and negative mechanism of transcriptional regulation
Published in FEBS letters (26-03-2004)“…We recently published the genomic characterization of the STAT5A and STAT5B paralogous genes that are located head to head in the 17q21 chromosome and share…”
Get full text
Journal Article -
13
MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions
Published in BMC medical genetics (04-05-2007)“…Cognitive impairments are heterogeneous conditions, and it is estimated that 10% may be caused by a defect of mental function genes on the X chromosome. One of…”
Get full text
Journal Article -
14
Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report
Published in BMC medical genetics (11-04-2007)“…The association between premature ovarian failure (POF) and the FMR1 repeat number (41> CGGn< 200) has been widely investigated. Current findings suggest that…”
Get full text
Journal Article -
15
VAMP subfamilies identified by specific R-SNARE motifs
Published in Biology of the cell (01-05-2004)“…In eukaryotes, interactions among the α-helical coiled-coil domains (CCDs) of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs)…”
Get full text
Journal Article -
16
Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains
Published in Human mutation (01-08-2001)“…X‐linked Retinitis Pigmentosa (XLRP) shows a huge genetic heterogeneity with almost five distinct loci on the X chromosome. So far, only two XLRP genes have…”
Get full text
Journal Article -
17
The structure of human STAT5A and B genes reveals two regions of nearly identical sequence and an alternative tissue specific STAT5B promoter
Published in Gene (20-02-2002)“…STAT5A and STAT5B genes belong to the signal transducer and activators of transcription (STAT) family of transcription factors. They show a high degree of…”
Get full text
Journal Article -
18
DNA Methylation in Transcriptional Repression of Two Differentially Expressed X-Linked Genes, GPC3 and SYBL1
Published in Proceedings of the National Academy of Sciences - PNAS (19-01-1999)“…Methylation of CpG islands is an established transcriptional repressive mechanism and is a feature of silencing in X chromosome inactivation. Housekeeping…”
Get full text
Journal Article -
19
Maximally Sparse Arrays Via Sequential Convex Optimizations
Published in IEEE antennas and wireless propagation letters (2012)“…The design of sparse arrays able to radiate focused beam patterns satisfying a given upper-bound power mask with the minimum number of sources is a research…”
Get full text
Journal Article -
20
Pulse-Shaping Strategy for Time Modulated Arrays-Analysis and Design
Published in IEEE transactions on antennas and propagation (01-07-2013)“…Time-modulated arrays (TMAs) are antenna systems where the transmitted or received signal is modulated by periodic time pulses. Several strategies have been…”
Get full text
Journal Article