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1
10 nm RecA protein filaments formed in the presence of Mg2+ and ATPγS may contain RNA
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10 nm RecA protein filaments formed in the presence of Mg2+ and ATPγS may contain RNA

REGISTER, J. C. III ; GRIFFITH, J

Molecular & general genetics, 1985-01, Vol.199 (3), p.415-420

Heidelberg: Springer

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2
14-3-3 proteins; bringing new definitions to scaffolding
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14-3-3 proteins; bringing new definitions to scaffolding

Tzivion, G ; Shen, Y H ; Zhu, J

Oncogene, 2001-10, Vol.20 (44), p.6331-6338 [Periódico revisado por pares]

England: Nature Publishing Group

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3
1448C mutation linked to the Pv1.1- genotype in Italian patients with Gaucher disease
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1448C mutation linked to the Pv1.1- genotype in Italian patients with Gaucher disease

TUTEJA, R ; BEMBI, B ; AGOSTI, E ; BARALLE, F. E

Human molecular genetics, 1993-06, Vol.2 (6), p.781-784 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
15-lipoxygenase-2 gene regulation by its product 15-(S)-hydroxyeicosatetraenoic acid through a negative feedback mechanism that involves peroxisome proliferator-activated receptor γ
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15-lipoxygenase-2 gene regulation by its product 15-(S)-hydroxyeicosatetraenoic acid through a negative feedback mechanism that involves peroxisome proliferator-activated receptor γ

SUBBARAYAN, V ; KRIEG, P ; LIPPMAN, S. M ; MENTER, D. G ; HSI, L. C ; KIM, J ; YANG, P ; SABICHI, A. L ; LLANSA, N ; MENDOZA, G ; LOGOTHETIS, C. J ; NEWMAN, R. A

Oncogene, 2006-09, Vol.25 (44), p.6015-6025 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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5
15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain
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15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain

Yasui, Dag H ; Scoles, Haley A ; Horike, Shin-ichi ; Meguro-Horike, Makiko ; Dunaway, Keith W ; Schroeder, Diane I ; LaSalle, Janine M

Human molecular genetics, 2011-11, Vol.20 (22), p.4311-4323 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
17-DMAG ameliorates polyglutamine-mediated motor neuron degeneration through well-preserved proteasome function in an SBMA model mouse
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17-DMAG ameliorates polyglutamine-mediated motor neuron degeneration through well-preserved proteasome function in an SBMA model mouse

Tokui, Keisuke ; Adachi, Hiroaki ; Waza, Masahiro ; Katsuno, Masahisa ; Minamiyama, Makoto ; Doi, Hideki ; Tanaka, Keiji ; Hamazaki, Jun ; Murata, Shigeo ; Tanaka, Fumiaki ; Sobue, Gen

Human molecular genetics, 2009-03, Vol.18 (5), p.898-910 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations
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17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations

VERGULT, Sarah ; DAUBER, Andrew ; MOHAMMED, Shehla ; OGILVIE, Caroline ; CROLLA, John ; MORTIER, Geert ; MENTEN, Bjorn ; DELLE CHIAIE, Barbara ; VAN OUDENHOVE, Elke ; SIMON, Marleen ; RIHANI, Ali ; LOEYS, Bart ; HIRSCHHORN, Joel ; PFOTENHAUER, Jean ; PHILLIPS, John A

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.534-539 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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8
187-gene phylogeny of protozoan phylum Amoebozoa reveals a new class (Cutosea) of deep-branching, ultrastructurally unique, enveloped marine Lobosa and clarifies amoeba evolution
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187-gene phylogeny of protozoan phylum Amoebozoa reveals a new class (Cutosea) of deep-branching, ultrastructurally unique, enveloped marine Lobosa and clarifies amoeba evolution

Cavalier-Smith, Thomas ; Chao, Ema E. ; Lewis, Rhodri

Molecular phylogenetics and evolution, 2016-06, Vol.99, p.275-296 [Periódico revisado por pares]

United States: Elsevier Inc

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9
2-Aminopurine and 5-bromouracil induce alleviation of type I restriction in Escherichia coli: mismatches function as inducing signals?
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2-Aminopurine and 5-bromouracil induce alleviation of type I restriction in Escherichia coli: mismatches function as inducing signals?

EFIMOVA, E. P ; DELVER, E. P ; BELOGUROV, A. A

Molecular & general genetics, 1988-10, Vol.214 (2), p.317-320 [Periódico revisado por pares]

Heidelberg: Springer

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10
A 16-bp RBE element mediated Rep-dependent site-specific integration in AAVS1 transgenic mice for expression of hFIX
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A 16-bp RBE element mediated Rep-dependent site-specific integration in AAVS1 transgenic mice for expression of hFIX

XU, Z. X ; CHEN, J. Z ; JIA, W ; YUE, Y. B ; ZHANG, J. Q ; LI, Z. H ; FENG, D. M ; RUAN, Z. C ; TIAN, L ; XUE, J. L ; WANG, Q. J

Gene therapy, 2009-05, Vol.16 (5), p.589-595 [Periódico revisado por pares]

London: Nature Publishing Group

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