نتایج جستجو برای: xeroderma pigmentosum xp

تعداد نتایج: 4493  

2013
Abigail Lubin Ling Zhang Hua Chen Victoria M. White Feng Gong

Global genome nucleotide excision repair (GG-NER) is responsible for identifying and removing bulky adducts from non-transcribed DNA that result from damaging agents such as UV radiation and cisplatin. Xeroderma pigmentosum complementation group C (XPC) is one of the essential damage recognition proteins of the GG-NER pathway and its dysfunction results in xeroderma pigmentosum (XP), a disorder...

2013
Jin-Ping Lai Yen-Chun Liu Meghna Alimchandani Qingyan Liu Phyu Phyu Aung Kant Matsuda Chyi-Chia R Lee Maria Tsokos Stephen Hewitt Elisabeth J Rushing Deborah Tamura David L Levens John J DiGiovanna Howard A Fine Nicholas Patronas Sikandar G Khan David E Kleiner J Carl Oberholtzer Martha M Quezado Kenneth H Kraemer

BACKGROUND To investigate the association of DNA nucleotide excision repair (NER) defects with neurological degeneration, cachexia and cancer, we performed autopsies on 4 adult xeroderma pigmentosum (XP) patients with different clinical features and defects in NER complementation groups XP-A, XP-C or XP-D. RESULTS The XP-A (XP12BE) and XP-D (XP18BE) patients exhibited progressive neurological...

Journal: :Journal of preventive medicine and hygiene 2010
L Feller N H Wood M H Motswaledi R A G Khammissa M Meyer J Lemmer

Inherited molecular defects in nucleotide excision repair genes cause the autosomal recessive condition xeroderma pigmentosum. Xeroderma pigmentosum is characterized by photo-hypersensitivity of sun-exposed tissues, and by a several thousand-fold increase in the risk of developing malignant neoplasms of the skin and of the eyes. Mutations in xeroderma pigmentosum genes that regulate nucleotide ...

Journal: :Nature communications 2015
Jue Er Amanda Lee Naomi C Mitchell Olga Zaytseva Arjun Chahal Peter Mendis Amandine Cartier-Michaud Linda M Parsons Gretchen Poortinga David L Levens Ross D Hannan Leonie M Quinn

Nucleotide excision DNA repair (NER) pathway mutations cause neurodegenerative and progeroid disorders (xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD)), which are inexplicably associated with (XP) or without (CS/TTD) cancer. Moreover, cancer progression occurs in certain patients, but not others, with similar C-terminal mutations in the XPB helicase subunit of ...

2017
Kamlen Pillay Saleigh Adams Laura Vandermaesen Donald Anthony Hudson

We report a 7-year-old girl with xeroderma pigmentosum (XP), who presented in our clinic with a large melanoma (35 × 50 × 20 mm, Breslow depth 18 mm) in the zygomatic-malar area. Palliative surgery was performed to maintain her residual vision and to reduce the pain caused by the compression of local structures. Because of the limited access of autologous skin grafts in pediatric patients with ...

2015
Karina Miranda Santiago Amanda França de Nóbrega Rafael Malagoli Rocha Silvia Regina Rogatto Maria Isabel Achatz

Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder characterized by DNA repair defects that cause photophobia, sunlight-induced cancers, and neurodegeneration. Prevalence of germline mutations in the nucleotide excision repair gene XPA vary significantly in different populations. No Brazilian patients have been reported to carry a germline mutation in this gene. In this study, th...

2006
W. Keijzer M. P. Mulder J. C. M. Langeveld E. M. E. Smit J. L. Bos D. Bootsma J. H. J. Hoeijmakers

Patients suffering from the genetic disorder xeroderma pigmentosum (XP) display an extreme sensitivity of their skin to sun (UV) exposure and predisposition to skin cancer due to deficiencies in the excision DNA repair pathway. Here we describe the establishment and characteriza tion of the first tumor cell line derived from an XP patient (belonging to complementation group C). The melanoma cel...

Journal: :Journal of medical genetics 1986
F P Imray A Hockey W Relf R G Ramsay C Kidson

An Australian family is described in which a mild form of xeroderma pigmentosum (XP) is inherited as an autosomal dominant trait. Studies of lymphoblastoid cells and fibroblasts from affected persons demonstrated cellular sensitivity to ultraviolet (UV) light as judged by diminished clonogenicity and higher frequencies of UV induced chromosome aberrations compared to normal controls. After UV i...

2013
Sophie Rouanet Emilie Warrick Yannick Gache Sabine Scarzello Marie-Françoise Avril Françoise Bernerd Thierry Magnaldo

Somatic stem cells ensure tissue renewal along life and healing of injuries. Their safe isolation, genetic manipulation ex vivo and reinfusion in patients suffering from life threatening immune deficiencies (for example, severe combined immunodeficiency (SCID)) have demonstrated the efficacy of ex vivo gene therapy. Similarly, adult epidermal stem cells have the capacity to renew epidermis, the...

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