Literature DB >> 7712653

Bloom's syndrome.

J German1.   

Abstract

Bloom's syndrome is a rare autosomal recessively transmitted disorder, the main clinical feature of which is small body size. A sun-sensitive, erythematous facial skin lesion, an excess of well-demarcated hyper- and hypopigmented skin lesions located anywhere on the body, and increased numbers of bacterial infections due to immunodeficiency are accompanying features of diagnostic value. In Bloom's syndrome, the complications are formidable: cancer, chronic lung disease, and diabetes. Cancers of the types and sites seen in the general population arise frequently and unusually early. Bloom's syndrome cells are hypermutable, and excessive numbers of somatic mutations are responsible for many of the clinical features. The clinical diagnosis is confirmed cytogenetically by demonstrating a characteristic chromosome instability.

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Year:  1995        PMID: 7712653

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  51 in total

1.  The Bloom's syndrome gene product promotes branch migration of holliday junctions.

Authors:  J K Karow; A Constantinou; J L Li; S C West; I D Hickson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

2.  The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases.

Authors:  P Mohaghegh; J K Karow; R M Brosh; V A Bohr; I D Hickson
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

3.  Cytokinesis failure occurs in Fanconi anemia pathway-deficient murine and human bone marrow hematopoietic cells.

Authors:  Patrizia Vinciguerra; Susana A Godinho; Kalindi Parmar; David Pellman; Alan D D'Andrea
Journal:  J Clin Invest       Date:  2010-11       Impact factor: 14.808

4.  RMI1 promotes DNA replication fork progression and recovery from replication fork stress.

Authors:  Jay Yang; Lara O'Donnell; Daniel Durocher; Grant W Brown
Journal:  Mol Cell Biol       Date:  2012-05-29       Impact factor: 4.272

5.  Bloom syndrome with lung involvement.

Authors:  Girija Nair; Ivona Lobo; T K Jayalaksmi; Abhay Uppe; Savita Jindal; Abhishek Chandra; Shivani Swami
Journal:  Lung India       Date:  2009-07

Review 6.  RecQ helicases in DNA double strand break repair and telomere maintenance.

Authors:  Dharmendra Kumar Singh; Avik K Ghosh; Deborah L Croteau; Vilhelm A Bohr
Journal:  Mutat Res       Date:  2011-06-13       Impact factor: 2.433

7.  RTEL1 maintains genomic stability by suppressing homologous recombination.

Authors:  Louise J Barber; Jillian L Youds; Jordan D Ward; Michael J McIlwraith; Nigel J O'Neil; Mark I R Petalcorin; Julie S Martin; Spencer J Collis; Sharon B Cantor; Melissa Auclair; Heidi Tissenbaum; Stephen C West; Ann M Rose; Simon J Boulton
Journal:  Cell       Date:  2008-10-17       Impact factor: 41.582

8.  Disruption of Supv3L1 damages the skin and causes sarcopenia, loss of fat, and death.

Authors:  Erin Paul; Rachel Cronan; Paula J Weston; Kim Boekelheide; John M Sedivy; Sang-Yun Lee; David L Wiest; Murray B Resnick; Jan E Klysik
Journal:  Mamm Genome       Date:  2009-01-15       Impact factor: 2.957

9.  HRAD1 and MRAD1 encode mammalian homologues of the fission yeast rad1(+) cell cycle checkpoint control gene.

Authors:  C M Udell; S K Lee; S Davey
Journal:  Nucleic Acids Res       Date:  1998-09-01       Impact factor: 16.971

10.  Bloom syndrome: multiple retinopathies in a chromosome breakage disorder.

Authors:  R B Bhisitkul; M Rizen
Journal:  Br J Ophthalmol       Date:  2004-03       Impact factor: 4.638

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