Genomic instability and DNA replication defects in progeroid syndromes

R Burla, M La Torre, C Merigliano, F Vernì, I Saggio - Nucleus, 2018 - Taylor & Francis
Progeroid syndromes induced by mutations in lamin A or in its interactors–named progeroid
laminopathies–are model systems for the dissection of the molecular pathways causing …

An inherited LMNA gene mutation in atypical Progeria syndrome

Y Doubaj, A De Sandre‐Giovannoli… - American Journal of …, 2012 - Wiley Online Library
Abstract Hutchinson–Gilford Progeria syndrome (HGPS) is a rare genetic disorder,
characterized by several clinical features that begin in early childhood, recalling an …

Atypical Progeria Primarily Manifesting as Premature Cardiac Valvular Disease Segregates with LMNA-Gene Variants

HW Wu, IP Van de Peppel, JW Rutten… - Journal of …, 2024 - mdpi.com
Mutations in the LMNA-gene can cause a variety of 'laminopathies'. These laminopathies
are associated with a range of phenotypes, including disorders affecting the adipose tissue …

The effect of the dengue non-structural 1 protein expression over the HepG2 cell proteins in a proteomic approach

K Rabelo, MRO Trugilho, SM Costa, BAS Pereira… - Journal of …, 2017 - Elsevier
Dengue is an important mosquito borne viral disease in the world. Dengue virus (DENV)
encodes a polyprotein, which is cleaved in ten proteins, including the non-structural protein …

Genetics of Human Laminopathies

G Novelli, MR D'Apice - eLS - Wiley Online Library
Lamins A/C, encoded by LMNA gene, are constituents of the nuclear lamina, a meshwork of
proteins underneath the nuclear envelope. Human disorders linked to LMNA mutations are …

Desnutrição e as implicações na cavidade oral

GJB Maia - 2015 - search.proquest.com
INSTITUTO SUPERIOR DE CIÊNCIAS DA SAÚDE EGAS MONIZ Page 1 INSTITUTO
SUPERIOR DE CIÊNCIAS DA SAÚDE EGAS MONIZ MESTRADO INTEGRADO EM …