Giovanna Lattanzi
Overview
Explore the profile of Giovanna Lattanzi including associated specialties, affiliations and a list of published articles.
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114
Citations
2272
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Recent Articles
1.
Paganelli F, Poli A, Truocchio S, Martelli A, Palumbo C, Lattanzi G, et al.
MedComm (2020)
. 2025 Jan;
6(2):e70073.
PMID: 39866838
Historically considered downstream effects of tumorigenesis-arising from changes in DNA content or chromatin organization-nuclear alterations have long been seen as mere prognostic markers within a genome-centric model of cancer. However,...
2.
Lattanzi G, Lanzuolo C, Cugudda E, Maggi L, Politano L, Santiago-Fernandez O, et al.
Aging Cell
. 2024 Dec;
23(12):e14414.
PMID: 39663551
No abstract available.
3.
Burla R, Carcuro M, La Torre M, Fratini F, Crescenzi M, DApice M, et al.
Open Biol
. 2024 Nov;
14(11):240314.
PMID: 39532151
No abstract available.
4.
Ceccarini G, Akinci B, Araujo-Vilar D, Beghini M, Brown R, Carrion Tudela J, et al.
Ann Endocrinol (Paris)
. 2024 Mar;
85(4):308-316.
PMID: 38452868
Lipodystrophy syndromes are rare diseases primarily affecting the development or maintenance of the adipose tissue but are also distressing indirectly multiple organs and tissues, often leading to reduced life expectancy...
5.
Cenni V, Evangelisti C, Santi S, Sabatelli P, Neri S, Cavallo M, et al.
Cells
. 2024 Jan;
13(2).
PMID: 38247853
In muscle cells subjected to mechanical stimulation, LINC complex and cytoskeletal proteins are basic to preserve cellular architecture and maintain nuclei orientation and positioning. In this context, the role of...
6.
Marchionni E, DApice M, Lupo V, Lattanzi G, Mattioli E, Lisignoli G, et al.
Bone Rep
. 2023 Dec;
19:101728.
PMID: 38076483
gene encodes the alpha-1 chain of type-II procollagen. Heterozygous pathogenic variants are associated with the broad clinical spectrum of genetic diseases known as type-II collagenopathies. We aimed to characterize the...
7.
Schena E, Mattioli E, Peres C, Zanotti L, Morselli P, Iozzo P, et al.
Cells
. 2023 Nov;
12(22).
PMID: 37998321
Type-2 Familial Partial Lipodystrophy (FPLD2), a rare lipodystrophy caused by mutations, is characterized by a loss of subcutaneous fat from the trunk and limbs and excess accumulation of adipose tissue...
8.
Crochemore C, Chica C, Garagnani P, Lattanzi G, Horvath S, Sarasin A, et al.
Aging Cell
. 2023 Sep;
22(10):e13959.
PMID: 37688320
Cockayne syndrome (CS) and UV-sensitive syndrome (UVSS) are rare genetic disorders caused by mutation of the DNA repair and multifunctional CSA or CSB protein, but only CS patients display a...
9.
Hartinger R, Lederer E, Schena E, Lattanzi G, Djabali K
Cells
. 2023 Jul;
12(10).
PMID: 37408186
Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disease that causes premature aging symptoms, such as vascular diseases, lipodystrophy, loss of bone mineral density, and alopecia. HGPS is mostly linked...
10.
Capanni C, Schena E, Di Giampietro M, Montecucco A, Mattioli E, Lattanzi G
Front Cell Dev Biol
. 2022 Dec;
10:1018102.
PMID: 36467410
Lamin A is a main constituent of the nuclear lamina and contributes to nuclear shaping, mechano-signaling transduction and gene regulation, thus affecting major cellular processes such as cell cycle progression...