Beatrice Schuster
Overview
Explore the profile of Beatrice Schuster including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
802
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Recent Articles
1.
Bogliolo M, Schuster B, Stoepker C, Derkunt B, Su Y, Raams A, et al.
Am J Hum Genet
. 2013 Apr;
92(5):800-6.
PMID: 23623386
Fanconi anemia (FA) is a rare genomic instability disorder characterized by progressive bone marrow failure and predisposition to cancer. FA-associated gene products are involved in the repair of DNA interstrand...
2.
Knies K, Schuster B, Ameziane N, Rooimans M, Bettecken T, de Winter J, et al.
PLoS One
. 2013 Jan;
7(12):e52648.
PMID: 23285130
Fanconi anemia (FA) is a rare genomic instability syndrome. Disease-causing are biallelic mutations in any one of at least 15 genes encoding members of the FA/BRCA pathway of DNA-interstrand crosslink...
3.
Schuster B, Knies K, Stoepker C, Velleuer E, Friedl R, Gottwald-Muhlhauser B, et al.
Hum Mutat
. 2012 Oct;
34(1):93-6.
PMID: 23033263
Fanconi anemia (FA) is a rare genetic disorder characterized by congenital malformations, progressive bone marrow failure (BMF), and susceptibility to malignancies. FA is caused by biallelic or hemizygous mutations in...
4.
Trujillo J, Mina L, Pujol R, Bogliolo M, Andrieux J, Holder M, et al.
Blood
. 2012 May;
120(1):86-9.
PMID: 22611161
Fanconi anemia (FA) is a rare bone marrow failure disorder with defective DNA interstrand crosslink repair. Still, there are FA patients without mutations in any of the 15 genes individually...
5.
Stoepker C, Hain K, Schuster B, Hilhorst-Hofstee Y, Rooimans M, Steltenpool J, et al.
Nat Genet
. 2011 Jan;
43(2):138-41.
PMID: 21240277
DNA interstrand crosslink repair requires several classes of proteins, including structure-specific endonucleases and Fanconi anemia proteins. SLX4, which coordinates three separate endonucleases, was recently recognized as an important regulator of...
6.
Kopic S, Eirich K, Schuster B, Hanenberg H, Varon-Mateeva R, Rittinger O, et al.
Acta Paediatr
. 2010 Dec;
100(5):780-3.
PMID: 21138478
Case Report: Hepatoblastoma was diagnosed in a 4-year-old girl receiving growth hormone substitution therapy for short stature. Owing to multiple congenital malformations, VACTERL-H (vertebral, anal, cardiac, tracheal, renal and limb...
7.
Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V, et al.
Nat Genet
. 2010 Apr;
42(5):406-9.
PMID: 20400963
Fanconi anemia (FA) is a rare chromosomal-instability disorder associated with a variety of developmental abnormalities, bone marrow failure and predisposition to leukemia and other cancers. We have identified a homozygous...
8.
Yan Z, Delannoy M, Ling C, Daee D, Osman F, Muniandy P, et al.
Mol Cell
. 2010 Mar;
37(6):865-78.
PMID: 20347428
FANCM remodels branched DNA structures and plays essential roles in the cellular response to DNA replication stress. Here, we show that FANCM forms a conserved DNA-remodeling complex with a histone-fold...
9.
Lang M, Zhang F, Zhang J, Wang J, Schuster B, Trautmann C, et al.
Nat Mater
. 2009 Sep;
8(10):793-7.
PMID: 19734884
High-pressure and high-temperature phases show unusual physical and chemical properties, but they are often difficult to 'quench' to ambient conditions. Here, we present a new approach, using bombardment with very...