نتایج جستجو برای: premature aging

تعداد نتایج: 161300  

Journal: :The Journal of biological chemistry 2011
Daniela Volonte Ferruccio Galbiati

According to the "free radical theory" of aging, premature senescence induced by oxidative stress contributes to organismal aging. Polymerase I and transcript release factor (PTRF)/cavin-1 is a structural protein component of caveolae, invaginations of the plasma membrane involved in signal transduction. We show that oxidative stress up-regulates PTRF/cavin-1 protein expression and promotes the...

Journal: :International Journal of Environmental Research and Public Health 2021

Over the last hundred years, life expectancy in developed countries has increased because of healthier living habits and treatment chronic pathologies causing premature aging. Aging is an inexorable, time-dependent, multifactorial process characterized by a series progressive irreversible physiological changes associated with loss functional, psychological, social capabilities. Numerous factors...

2007
Robert M. Brosh Vilhelm A. Bohr

Genomic instability leads to mutations, cellular dysfunction and aberrant phenotypes at the tissue and organism levels. A number of mechanisms have evolved to cope with endogenous or exogenous stress to prevent chromosomal instability and maintain cellular homeostasis. DNA helicases play important roles in the DNA damage response. The RecQ family of DNA helicases is of particular interest since...

Journal: :Trends in biochemical sciences 2001
J E Cleaver

Genomic instability is the driving force behind cancer development. Human syndromes with DNA repair deficiencies comprise unique opportunities to study the clinical consequences of faulty genome maintenance leading to premature aging and premature cancer development. These syndromes include chromosomal breakage syndromes with defects in DNA damage signal transduction and double-strand break rep...

2014
Sylvia Koch Omar Garcia Gonzalez Robin Assfalg Adrian Schelling Patrick Schäfer Karin Scharffetter-Kochanek Sebastian Iben

Mutations in the Cockayne syndrome A (CSA) protein account for 20% of Cockayne syndrome (CS) cases, a childhood disorder of premature aging and early death. Hitherto, CSA has exclusively been described as DNA repair factor of the transcription-coupled branch of nucleotide excision repair. Here we show a novel function of CSA as transcription factor of RNA polymerase I in the nucleolus. Knockdow...

Journal: :AANA journal 1994
F C O'Brien B Ginsberg

A 4-year-old female with Cockayne syndrome presented for cataract extraction under general anesthesia. She was thin and frail; her neck, epiglottis and larynx were stiff; she was deaf and blind; and she could not speak, sit unaided, or perspire. At the time of her admission, she weighed 5.5 kg. Cockayne syndrome is a disease of childhood characterized by mental retardation and premature aging. ...

Journal: :Trends in molecular medicine 2010
Martine Caron-Debarle Claire Lagathu Franck Boccara Corinne Vigouroux Jacqueline Capeau

Combination antiretroviral therapy (cART) against HIV infection dramatically reduces AIDS-related morbidity. However, many patients under cART display HIV-associated lipodystrophy. Moreover, some develop early age-related comorbidities. Thymidine analog reverse transcriptase inhibitors (tRNTIs) are mainly responsible for peripheral lipoatrophy, and protease inhibitors (PIs) for fat hypertrophy ...

Journal: :Experimental dermatology 2007
Kai-Martin Thoms Christiane Kuschal Steffen Emmert

Genomic instability is the driving force behind cancer development. Human syndromes with DNA repair deficiencies comprise unique opportunities to study the clinical consequences of faulty genome maintenance leading to premature aging and premature cancer development. These syndromes include chromosomal breakage syndromes with defects in DNA damage signal transduction and double-strand break rep...

2011
Simona Baronchelli Donatella Conconi Elena Panzeri Angela Bentivegna Serena Redaelli Sara Lissoni Fabiana Saccheri Nicoletta Villa Francesca Crosti Elena Sala Emanuela Martinoli Marinella Volontè Anna Marozzi Leda Dalprà

The importance of X chromosome in the aetiology of premature ovarian failure (POF) is well-known but in many cases POF still remains idiopathic. Chromosome aneuploidy increase is a physiological phenomenon related to aging, but the role of low-level sex chromosome mosaicism in ovarian function is still undiscovered. Standard cytogenetic analysis was carried out in a total of 269 patients affect...

Journal: :Handbook of clinical neurology 2015
Nicole J Ullrich Leslie B Gordon

Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare, uniformly fatal, segmental "premature aging" disease in which children exhibit phenotypes that may give us insights into the aging process at both the cellular and organismal levels. Initial presentation in early childhood is primarily based on growth and dermatologic findings. Primary morbidity and mortality for children with HG...

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