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1
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
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Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus

Yang, Wanling ; Shen, Nan ; Ye, Dong-Qing ; Liu, Qiji ; Zhang, Yan ; Qian, Xiao-Xia ; Hirankarn, Nattiya ; Ying, Dingge ; Pan, Hai-Feng ; Mok, Chi Chiu ; Chan, Tak Mao ; Wong, Raymond Woon Sing ; Lee, Ka Wing ; Mok, Mo Yin ; Wong, Sik Nin ; Leung, Alexander Moon Ho ; Li, Xiang-Pei ; Avihingsanon, Yingyos ; Wong, Chun-Ming ; Lee, Tsz Leung ; Ho, Marco Hok Kung ; Lee, Pamela Pui Wah ; Chang, Yuk Kwan ; Li, Philip H ; Li, Ruo-Jie ; Zhang, Lu ; Wong, Wilfred Hing Sang ; Ng, Irene Oi Lin ; Lau, Chak Sing ; Sham, Pak Chung ; Lau, Yu Lung Flint, Jonathan

PLoS genetics, 2010-02, Vol.6 (2), p.e1000841-e1000841 [Periódico revisado por pares]

United States: Public Library of Science

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2
Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways
Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways
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Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways

Tang, Chen-Yi ; Wu, Mengrui ; Zhao, Dongfeng ; Edwards, Diep ; McVicar, Abigail ; Luo, Yuan ; Zhu, Guochun ; Wang, Yongjun ; Zhou, Hou-De ; Chen, Wei ; Li, Yi-Ping LONG, FANXIN

PLoS genetics, 2021-01, Vol.17 (1), p.e1009233-e1009233 [Periódico revisado por pares]

United States: Public Library of Science

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3
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients
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Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Inoue, Takanobu ; Nakamura, Akie ; Iwahashi-Odano, Megumi ; Tanase-Nakao, Kanako ; Matsubara, Keiko ; Nishioka, Junko ; Maruo, Yoshihiro ; Hasegawa, Yukihiro ; Suzumura, Hiroshi ; Sato, Seiji ; Kobayashi, Yoshiyuki ; Murakami, Nobuyuki ; Nakabayashi, Kazuhiko ; Yamazawa, Kazuki ; Fuke, Tomoko ; Narumi, Satoshi ; Oka, Akira ; Ogata, Tsutomu ; Fukami, Maki ; Kagami, Masayo

Clinical epigenetics, 2020-06, Vol.12 (1), p.86-86, Article 86 [Periódico revisado por pares]

Germany: BioMed Central Ltd

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4
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci
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A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci

Liu, Ying ; Helms, Cynthia ; Liao, Wilson ; Zaba, Lisa C ; Duan, Shenghui ; Gardner, Jennifer ; Wise, Carol ; Miner, Andrew ; Malloy, M J ; Pullinger, Clive R ; Kane, John P ; Saccone, Scott ; Worthington, Jane ; Bruce, Ian ; Kwok, Pui-Yan ; Menter, Alan ; Krueger, James ; Barton, Anne ; Saccone, Nancy L ; Bowcock, Anne M Leal, Suzanne M.

PLoS genetics, 2008-04, Vol.4 (3), p.e1000041-e1000041 [Periódico revisado por pares]

United States: Public Library of Science

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5
The role of nucleosome positioning in the evolution of gene regulation
The role of nucleosome positioning in the evolution of gene regulation
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The role of nucleosome positioning in the evolution of gene regulation

Tsankov, Alexander M ; Thompson, Dawn Anne ; Socha, Amanda ; Regev, Aviv ; Rando, Oliver J Becker, Peter B.

PLoS biology, 2010-07, Vol.8 (7), p.e1000414 [Periódico revisado por pares]

United States: Public Library of Science

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6
Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host
Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host
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Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host

Nikoh, Naruo ; McCutcheon, John P ; Kudo, Toshiaki ; Miyagishima, Shin-ya ; Moran, Nancy A ; Nakabachi, Atsushi Copenhaver, Gregory P.

PLoS genetics, 2010-02, Vol.6 (2), p.e1000827-e1000827 [Periódico revisado por pares]

United States: Public Library of Science

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7
RNA-directed DNA Methylation
RNA-directed DNA Methylation
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RNA-directed DNA Methylation

Erdmann, Robert M ; Picard, Colette L

PLoS genetics, 2020-10, Vol.16 (10), p.e1009034-e1009034 [Periódico revisado por pares]

United States: Public Library of Science

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8
Genome-wide profiling of yeast DNA:RNA hybrid prone sites with DRIP-chip
Genome-wide profiling of yeast DNA:RNA hybrid prone sites with DRIP-chip
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Genome-wide profiling of yeast DNA:RNA hybrid prone sites with DRIP-chip

Chan, Yujia A ; Aristizabal, Maria J ; Lu, Phoebe Y T ; Luo, Zongli ; Hamza, Akil ; Kobor, Michael S ; Stirling, Peter C ; Hieter, Philip Snyder, Michael

PLoS genetics, 2014-04, Vol.10 (4), p.e1004288 [Periódico revisado por pares]

United States: Public Library of Science

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9
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study
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TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study

de Vries, Petrus J ; Belousova, Elena ; Benedik, Mirjana P ; Carter, Tom ; Cottin, Vincent ; Curatolo, Paolo ; Dahlin, Maria ; D'Amato, Lisa ; d'Augères, Guillaume B ; Ferreira, José C ; Feucht, Martha ; Fladrowski, Carla ; Hertzberg, Christoph ; Jozwiak, Sergiusz ; Kingswood, J Chris ; Lawson, John A ; Macaya, Alfons ; Marques, Ruben ; Nabbout, Rima ; O'Callaghan, Finbar ; Qin, Jiong ; Sander, Valentin ; Sauter, Matthias ; Shah, Seema ; Takahashi, Yukitoshi ; Touraine, Renaud ; Youroukos, Sotiris ; Zonnenberg, Bernard ; Jansen, Anna C

Orphanet journal of rare diseases, 2018-09, Vol.13 (1), p.157-157, Article 157 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation
Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation
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Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation

Zhong, Franklin L. ; Mamaï, Ons ; Sborgi, Lorenzo ; Boussofara, Lobna ; Hopkins, Richard ; Robinson, Kim ; Szeverényi, Ildikó ; Takeichi, Takuya ; Balaji, Reshmaa ; Lau, Aristotle ; Tye, Hazel ; Roy, Keya ; Bonnard, Carine ; Ahl, Patricia J. ; Jones, Leigh Ann ; Baker, Paul J. ; Lacina, Lukas ; Otsuka, Atsushi ; Fournie, Pierre R. ; Malecaze, François ; Lane, E. Birgitte ; Akiyama, Masashi ; Kabashima, Kenji ; Connolly, John E. ; Masters, Seth L. ; Soler, Vincent J. ; Omar, Salma Samir ; McGrath, John A. ; Nedelcu, Roxana ; Gribaa, Moez ; Denguezli, Mohamed ; Saad, Ali ; Hiller, Sebastian ; Reversade, Bruno

Cell, 2016-09, Vol.167 (1), p.187-202.e17 [Periódico revisado por pares]

United States: Elsevier Inc

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