Search Results

Effect of base sequence on the DNA cross-linking properties of pyrrolobenzodiazepine (PBD) dimers

• Authors : Rahman, KM; James, CH; Thurston, DE

• Source: Nucleic Acids Research , 39 (13) 5800 - 5812. (2011)

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Mapping the phylogeny and lineage history of geographically distinct BCG vaccine strains

• Authors : Elton, Linzy; Kasaragod, Sandeep; Donoghue, Helen

Subjects: BCG; Oxford Nanopore Technologies; long read

• Source: Microbial Genomics , 9 (8) , Article 001077. (2023)

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The complete sequence of a human Y chromosome

• Authors : Rhie, Arang; Nurk, Sergey; Cechova, Monika

Subjects: Humans; Base Sequence; Chromosomes

• Source: Nature , 621 (7978) pp. 344-354. (2023)

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Therapeutic gene editing in CD34+ hematopoietic progenitors from Fanconi anemia patients

• Authors : Diez, B; Genovese, P; Roman-Rodriguez, FJ

Subjects: CD34+ cells; Fanconi anemia; gene editing

• Source: EMBO Molecular Medicine , 9 (11) pp. 1574-1588. (2017)

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Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

• Authors : Nioi, P; Sigurdsson, A; Thorleifsson, G

Subjects: Adult; Aged; 80 and over

• Source: New England Journal of Medicine , 374 (22) pp. 2131-2141. (2016)

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Assessment of Minimal Residual Disease in Standard-Risk AML

• Authors : Ivey, A; Hills, RK; Simpson, MA

Subjects: Base Sequence; DNA; Neoplasm

• Source: The New England Journal Medicine , 374 (5) pp. 422-433. (2016)

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A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 gene

• Authors : Meunier, I; Bocquet, B; Labesse, G

Subjects: Aged; Base Sequence; Family

• Source: Scientific Reports , 6 , Article 32544. (2016)

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A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia

• Authors : Mencacci, NE; Rubio-Agusti, I; Zdebik, A

Subjects: Adaptor Proteins; Signal Transducing; Base Sequence

• Source: Am J Hum Genet , 96 (6) pp. 938-947. (2015)

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Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2.

• Authors : Cottenie, E; Kochanski, A; Jordanova, A

Subjects: Adult; Base Sequence; Charcot-Marie-Tooth Disease

• Source: Am J Hum Genet , 95 (5) 590 - 601. (2014)

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Recurrent PTPRB and PLCG1 mutations in angiosarcoma

• Authors : Behjati, S; Tarpey, PS; Sheldon, H

Subjects: Analysis of Variance; Base Sequence; Exome

• Source: Nature Genetics , 46 (4) 376 - 379. (2014)

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