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Refinado por: assunto: Molecular Sequence Data remover
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11
ske-T, a T-box gene expressed in the skeletogenic mesenchyme lineage of the sea urchin embryo
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ske-T, a T-box gene expressed in the skeletogenic mesenchyme lineage of the sea urchin embryo

Croce, Jenifer ; Lhomond, Guy ; Lozano, Jean-Claude ; Gache, Christian

Mechanisms of development, 2001-09, Vol.107 (1), p.159-162

Ireland: Elsevier Ireland Ltd

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12
Structure of the sea urchin hatching enzyme gene
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Structure of the sea urchin hatching enzyme gene

GHIGLIONE, Christian ; LHOMOND, Guy ; LEPAGE, Thierry ; GACHE, Christian

European journal of biochemistry, 1994-02, Vol.219 (3), p.845-854 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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13
Structure of the Gene Encoding the Sea Urchin Blastula Protease 10 (BP10), A Member of the Astacin Family of Zn2+–Metalloproteases
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Structure of the Gene Encoding the Sea Urchin Blastula Protease 10 (BP10), A Member of the Astacin Family of Zn2+–Metalloproteases

Lhomond, Guy ; Ghiglione, Christian ; Lepage, Thierry ; Gache, Christian

European journal of biochemistry, 1996-06, Vol.238 (3), p.744-751 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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14
Myosin XI-i Links the Nuclear Membrane to the Cytoskeleton to Control Nuclear Movement and Shape in Arabidopsis
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Myosin XI-i Links the Nuclear Membrane to the Cytoskeleton to Control Nuclear Movement and Shape in Arabidopsis

Tamura, Kentaro ; Iwabuchi, Kosei ; Fukao, Yoichiro ; Kondo, Maki ; Okamoto, Keishi ; Ueda, Haruko ; Nishimura, Mikio ; Hara-Nishimura, Ikuko

Current biology, 2013-09, Vol.23 (18), p.1776-1781 [Periódico revisado por pares]

England: Elsevier Ltd

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15
Mutation analysis and characterization of COL7A1 mutations in dystrophic epidermolysis bullosa
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Mutation analysis and characterization of COL7A1 mutations in dystrophic epidermolysis bullosa

Dang, Ningning ; Murrell, Dédée F.

Experimental dermatology, 2008-07, Vol.17 (7), p.553-568 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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16
Discovery of a second SALMFamide gene in the sea urchin Strongylocentrotus purpuratus reveals that L-type and F-type SALMFamide neuropeptides coexist in an echinoderm species
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Discovery of a second SALMFamide gene in the sea urchin Strongylocentrotus purpuratus reveals that L-type and F-type SALMFamide neuropeptides coexist in an echinoderm species

Rowe, Matthew L. ; Elphick, Maurice R.

Marine genomics, 2010-06, Vol.3 (2), p.91-97 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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17
The structure of the catalytic domain of Tannerella forsythia karilysin reveals it is a bacterial xenologue of animal matrix metalloproteinases
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The structure of the catalytic domain of Tannerella forsythia karilysin reveals it is a bacterial xenologue of animal matrix metalloproteinases

Cerdà‐Costa, Núria ; Guevara, Tibisay ; Karim, Abdulkarim Y. ; Ksiazek, Miroslaw ; Nguyen, Ky‐Anh ; Arolas, Joan L. ; Potempa, Jan ; Gomis‐Rüth, F. Xavier

Molecular microbiology, 2011-01, Vol.79 (1), p.119-132 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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18
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Leigh, I.M ; Bryant, S.P ; Milana, G ; Kirtschig, G ; Pulkkinen, L ; Smith, F.J.D ; McLean, W.H.I ; Eady, R.A.J ; Spurr, N.K ; Owaribe, K ; McMillan, J.R ; Lane, E.B ; Geddes, J.F ; de Bono, A.G ; Uitto, J ; Wiche, G ; Kelsell, D.P ; Rugg, E.L

Nature genetics, 1996-08, Vol.13 (4), p.450-457 [Periódico revisado por pares]

London: Nature Publishing Group

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19
Expression of wnt and frizzled genes during early sea star development
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Expression of wnt and frizzled genes during early sea star development

McCauley, Brenna S. ; Akyar, Eda ; Filliger, Laura ; Hinman, Veronica F.

Gene Expression Patterns, 2013-12, Vol.13 (8), p.437-444 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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20
A Site-Specific Plectin Mutation Causes Dominant Epidermolysis Bullosa Simplex Ogna: Two Identical De Novo Mutations
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A Site-Specific Plectin Mutation Causes Dominant Epidermolysis Bullosa Simplex Ogna: Two Identical De Novo Mutations

Koss-Harnes, Dörte ; Høyheim, Bjørn ; Anton-Lamprecht, Ingrun ; Gjesti, Aud ; Jørgensen, Randi S. ; Jahnsen, Frode L. ; Olaisen, Bjørnar ; Wiche, Gerhard ; Gedde-Dahl, Tobias

Journal of investigative dermatology, 2002-01, Vol.118 (1), p.87-93 [Periódico revisado por pares]

Danvers, MA: Elsevier Inc

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