نتائج البحث

Keplerian Black Holes and Gravitating Goldstones:Constructing relativistic systems with hidden symmetry and the double copy of field theories

• Authors : de Neeling, Dijs

• Source: de Neeling , D 2024 , ' Keplerian Black Holes and Gravitating Goldstones : Constructing relativistic systems with hidden symmetry and the double copy of field theories '

تفاصيل العنوان

LINE-1 expression in cancer correlates with p53 mutation, copy number alteration, and S phase checkpoint

• Authors : McKerrow, Wilson; Wang, Xuya; Mendez-Dorantes, Carlos

Subjects: retrotransposon; LINE-1; cancer

• Source: McKerrow, W, Wang, X, Mendez-Dorantes, C, Mita, P, Cao, S, Grivainis, M, Ding, L, LaCava, J, Burns, K H, Boeke, J D & Fenyo, D 2022, 'LINE-1 expression in cancer correlates with p53 mutation,

تفاصيل العنوان

Hybrid Goldstone Modes from the Double Copy Bootstrap

• Authors : Li, Yang; Roest, Diederik; ter Veldhuis, Tonnis

• Source: Li, Y, Roest, D & ter Veldhuis, T 2024, 'Hybrid Goldstone Modes from the Double Copy Bootstrap', Physical Review Letters, vol. 132, no. 21, 211602.

تفاصيل العنوان

Bertrand’s theorem and the double copy of relativistic field theories

• Authors : de Neeling, Dijs; Roest, Diederik; Seri, Marcello

Subjects: Black Holes; Classical Theories of Gravity; Space-Time Symmetries

• Source: de Neeling, D, Roest, D, Seri, M & Waalkens, H 2024, 'Bertrand’s theorem and the double copy of relativistic field theories', Journal of High Energy Physics, vol.

تفاصيل العنوان

The ELIXIR Human Copy Number Variations Community:building bioinformatics infrastructure for research

• Authors : Salgado, David; Armean, Irina M; Baudis, Michael

Subjects: Computational Biology; DNA Copy Number Variations/genetics; High-Throughput Nucleotide Sequencing

• Source: Salgado , D , Armean , I M , Baudis , M , Beltran , S , Capella-Gutierrez , S , Carvalho-Silva , D , Dominguez Del Angel , V , Dopazo , J , Furlong , L I , Gao , B , Garcia , L , Gerloff , D , Gut , I

تفاصيل العنوان

Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics

• Authors : Eijkelenboom, Astrid; Tops, Bastiaan B. J.; van den Berg, Anke

Subjects: Copy number gain; Amplification; NGS

• Source: Eijkelenboom, A, Tops, B B J, van den Berg, A, van den Brule, A J C, Dinjens, W N M, Dubbink, H J, ter Elst, A, Geurts-Giele, W R R, Groenen, P J T A, Groenendijk, F H, Heideman, D A M, Huibers, M M

تفاصيل العنوان

Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia

• Authors : Ghorbani, Fatemeh; de Boer, Eddy N; Benjamins-Stok, Marloes

• Source: Ghorbani, F, de Boer, E N, Benjamins-Stok, M, Verschuuren-Bemelmans, C C, Knapper, J, de Boer-Bergsma, J, de Vries, J J, Sikkema-Raddatz, B, Verbeek, D S, Westers, H & van Diemen, C C 2023, '

تفاصيل العنوان

Lexical and frequency effects on keystroke timing:Challenges to a lexical search account from a type-to-copy task.

• Authors : Feldman, Laurie Beth; Dale, Rick; van Rij, Jacolien

Subjects: type-to-copy task; written production; morpheme

• Source: Feldman , L B , Dale , R & van Rij , J 2019 , ' Lexical and frequency effects on keystroke timing : Challenges to a lexical search account from a type-to-copy task. ' ,

تفاصيل العنوان

Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses

• Authors : Shaikh, Nadeem; Mazzagatti, Alice; De Angelis, Simone

Subjects: COMMON FRAGILE SITES; ONCOGENE-INDUCED SENESCENCE; DAMAGE RESPONSE

• Source: Shaikh, N, Mazzagatti, A, De Angelis, S, Johnson, S C, Bakker, B, Spierings, D C J, Wardenaar, R, Maniati, E, Wang, J, Boemo, M A, Foijer, F & McClelland, S E 2022, 'Replication stress generates

تفاصيل العنوان

Review of genetic testing in kidney disease patients:Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups

• Authors : Claus, Laura R.; Snoek, Rozemarijn; Knoers, Nine V.A.M.

Subjects: CKD; CNV; diagnostic yield

• Source: Claus, L R, Snoek, R, Knoers, N V A M & van Eerde, A M 2022, 'Review of genetic testing in kidney disease patients : Diagnostic yield of single nucleotide variants and

تفاصيل العنوان