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A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes
A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes
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A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes

Oliveira Junior, Antonio B. ; Contessoto, Vinícius G. ; Mello, Matheus F. ; Onuchic, José N.

Journal of molecular biology, 2021-03, Vol.433 (6), p.166700-166700, Article 166700 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands
Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands
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Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands

Haller, Florian ; Bieg, Matthias ; Will, Rainer ; Körner, Cindy ; Weichenhan, Dieter ; Bott, Alexander ; Ishaque, Naveed ; Lutsik, Pavlo ; Moskalev, Evgeny A ; Mueller, Sarina K ; Bähr, Marion ; Woerner, Angelika ; Kaiser, Birgit ; Scherl, Claudia ; Haderlein, Marlen ; Kleinheinz, Kortine ; Fietkau, Rainer ; Iro, Heinrich ; Eils, Roland ; Hartmann, Arndt ; Plass, Christoph ; Wiemann, Stefan ; Agaimy, Abbas

Nature communications, 2019-01, Vol.10 (1), p.368-13, Article 368 [Periódico revisado por pares]

England: Nature Publishing Group

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3
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
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A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Vona, Barbara ; Mazaheri, Neda ; Lin, Sheng-Jia ; Dunbar, Lucy A. ; Maroofian, Reza ; Azaiez, Hela ; Booth, Kevin T. ; Vitry, Sandrine ; Rad, Aboulfazl ; Rüschendorf, Franz ; Varshney, Pratishtha ; Fowler, Ben ; Beetz, Christian ; Alagramam, Kumar N. ; Murphy, David ; Shariati, Gholamreza ; Sedaghat, Alireza ; Houlden, Henry ; Petree, Cassidy ; VijayKumar, Shruthi ; Smith, Richard J. H. ; Haaf, Thomas ; El-Amraoui, Aziz ; Bowl, Michael R. ; Varshney, Gaurav K. ; Galehdari, Hamid

Human genetics, 2021-06, Vol.140 (6), p.915-931 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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4
Structure, function and regulation of jade family PHD finger 1 (JADE1)
Structure, function and regulation of jade family PHD finger 1 (JADE1)
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Structure, function and regulation of jade family PHD finger 1 (JADE1)

Panchenko, Maria V.

Gene, 2016-09, Vol.589 (1), p.1-11 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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5
Association of rs6822844 within the KIAA1109/TENR/IL2/IL21 locus with rheumatoid arthritis in the Algerian population
Association of rs6822844 within the KIAA1109/TENR/IL2/IL21 locus with rheumatoid arthritis in the Algerian population
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Association of rs6822844 within the KIAA1109/TENR/IL2/IL21 locus with rheumatoid arthritis in the Algerian population

Louahchi, S. ; Allam, I. ; Raaf, N. ; Berkani, L. ; Boucharef, A. ; Abdessemed, A. ; Khaldoun, N. ; Bahaz, N. ; Ladjouze-Rezig, A. ; Nebbab, A. ; Ghaffor, M. ; Djidjik, R.

HLA, 2016-03, Vol.87 (3), p.160-164 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa
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Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa

Ali, Shahbaz ; Riazuddin, S Amer ; Shahzadi, Amber ; Nasir, Idrees A ; Khan, Shaheen N ; Husnain, Tayyab ; Akram, Javed ; Sieving, Paul A ; Hejtmancik, J Fielding ; Riazuddin, Sheikh

Molecular vision, 2011, Vol.17, p.1373-1380 [Periódico revisado por pares]

United States: Molecular Vision

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7
Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy
Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy
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Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy

Yang, Fan ; Shao, Chunbo ; Vedanarayanan, Vettaikorumakankav ; Ehrlich, Melanie

Chromosoma, 2004-05, Vol.112 (7), p.350-359 [Periódico revisado por pares]

Austria: Springer-Verlag

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8
Biophysical Study of the Globular Organisation of Interphase Chromosomes
Biophysical Study of the Globular Organisation of Interphase Chromosomes
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Biophysical Study of the Globular Organisation of Interphase Chromosomes

Eidelman, YuA ; Andreev, S G

Radiation protection dosimetry, 2002-01, Vol.99 (1-4), p.217-218 [Periódico revisado por pares]

England: Oxford University Press

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9
COMMON SEQUENCE MOTIFS AT THE REARRANGEMENT SITES OF A CONSTITUTIONAL-X AUTOSOME TRANSLOCATION AND ASSOCIATED DELETION
COMMON SEQUENCE MOTIFS AT THE REARRANGEMENT SITES OF A CONSTITUTIONAL-X AUTOSOME TRANSLOCATION AND ASSOCIATED DELETION
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COMMON SEQUENCE MOTIFS AT THE REARRANGEMENT SITES OF A CONSTITUTIONAL-X AUTOSOME TRANSLOCATION AND ASSOCIATED DELETION

GIACALONE, JP ; FRANCKE, U

American journal of human genetics, 1992-04, Vol.50 (4), p.725-741 [Periódico revisado por pares]

CAMBRIDGE: Elsevier

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10
Assignment of human satellite 1 DNA as revealed by fluorescent in situ hybridization with oligonucleotides
Assignment of human satellite 1 DNA as revealed by fluorescent in situ hybridization with oligonucleotides
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Assignment of human satellite 1 DNA as revealed by fluorescent in situ hybridization with oligonucleotides

TAGARRO, I ; WIEGANT, J ; RAAP, A. K ; GONZALEZ-AGUILERA, J. J ; FERNANDEZ-PERALTA, A. M

Human genetics, 1994-02, Vol.93 (2), p.125-128 [Periódico revisado por pares]

Heidelberg: Springer

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