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1
The common TMC1 mutation c.100C>T (p.Arg34X) is not a significant cause of deafness in British Asians
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The common TMC1 mutation c.100C>T (p.Arg34X) is not a significant cause of deafness in British Asians

Searle, Claire ; Mavrogiannis, Lampros A ; Bennett, Christopher P ; Charlton, Ruth S

Genetic testing and molecular biomarkers, 2012-05, Vol.16 (5), p.453-455 [Periódico revisado por pares]

United States

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2
The Microtus voles: Resolving the phylogeny of one of the most speciose mammalian genera using genomics
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Artigo
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The Microtus voles: Resolving the phylogeny of one of the most speciose mammalian genera using genomics

Barbosa, Soraia ; Paupério, Joana ; Pavlova, Svetlana V. ; Alves, Paulo C. ; Searle, Jeremy B.

Molecular phylogenetics and evolution, 2018-08, Vol.125, p.85-92 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Invadopodia are chemosensing protrusions that guide cancer cell extravasation to promote brain tropism in metastasis
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Invadopodia are chemosensing protrusions that guide cancer cell extravasation to promote brain tropism in metastasis

Williams, Karla C ; Cepeda, Mario A ; Javed, Sumreen ; Searle, Karlee ; Parkins, Katie M ; Makela, Ashley V ; Hamilton, Amanda M ; Soukhtehzari, Sepideh ; Kim, Yohan ; Tuck, Alan B ; Ronald, John A ; Foster, Paula J ; Chambers, Ann F ; Leong, Hon S

Oncogene, 2019-05, Vol.38 (19), p.3598-3615 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Phylogenetic relationships and the evolution of host preferences in the largest clade of brood parasitic bees (Apidae: Nomadinae)
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Artigo
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Phylogenetic relationships and the evolution of host preferences in the largest clade of brood parasitic bees (Apidae: Nomadinae)

Sless, Trevor J.L. ; Branstetter, Michael G. ; Gillung, Jessica P. ; Krichilsky, Erin A. ; Tobin, Kerrigan B. ; Straka, Jakub ; Rozen, Jerome G. ; Freitas, Felipe V. ; Martins, Aline C. ; Bossert, Silas ; Searle, Jeremy B. ; Danforth, Bryan N.

Molecular phylogenetics and evolution, 2022-01, Vol.166, p.107326-107326, Article 107326 [Periódico revisado por pares]

United States: Elsevier Inc

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5
The Ensembl analysis pipeline
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The Ensembl analysis pipeline

Potter, Simon C ; Clarke, Laura ; Curwen, Val ; Keenan, Stephen ; Mongin, Emmanuel ; Searle, Stephen M J ; Stabenau, Arne ; Storey, Roy ; Clamp, Michele

Genome research, 2004-05, Vol.14 (5), p.934-941 [Periódico revisado por pares]

United States: Cold Spring Harbor Laboratory Press

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6
Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project
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Artigo
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Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project

Peter, Michelle ; Hammond, Jennifer ; Sanderson, Saskia C ; Gurasashvili, Jana ; Hunter, Amy ; Searle, Beverly ; Patch, Christine ; Chitty, Lyn S ; Hill, Melissa ; Lewis, Celine

European journal of human genetics : EJHG, 2023-12, Vol.31 (12), p.1407-1413 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Molecular phylogeny of the speciose vole genus Microtus (Arvicolinae, Rodentia) inferred from mitochondrial DNA sequences
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Artigo
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Molecular phylogeny of the speciose vole genus Microtus (Arvicolinae, Rodentia) inferred from mitochondrial DNA sequences

Jaarola, Maarit ; Martínková, Natália ; Gündüz, İslam ; Brunhoff, Cecilia ; Zima, Jan ; Nadachowski, Adam ; Amori, Giovanni ; Bulatova, Nina S. ; Chondropoulos, Basil ; Fraguedakis-Tsolis, Stella ; González-Esteban, Jorge ; José López-Fuster, María ; Kandaurov, Andrei S. ; Kefelioğlu, Haluk ; da Luz Mathias, Maria ; Villate, Idoia ; Searle, Jeremy B.

Molecular phylogenetics and evolution, 2004-12, Vol.33 (3), p.647-663 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
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Artigo
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Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study

Peter, Michelle ; Hammond, Jennifer ; Sanderson, Saskia C ; Gurasashvili, Jana ; Hunter, Amy ; Searle, Beverly ; Patch, Christine ; Chitty, Lyn S ; Hill, Melissa ; Lewis, Celine

European journal of human genetics : EJHG, 2022-05, Vol.30 (5), p.604-610 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Development and mixed-methods evaluation of an online animation for young people about genome sequencing
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Artigo
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Development and mixed-methods evaluation of an online animation for young people about genome sequencing

Lewis, Celine ; Sanderson, Saskia C ; Hammond, Jennifer ; Hill, Melissa ; Searle, Beverly ; Hunter, Amy ; Patch, Christine ; Chitty, Lyn S

European journal of human genetics : EJHG, 2020-07, Vol.28 (7), p.896-906 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Towards a European consensus for reporting incidental findings during clinical NGS testing
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Artigo
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Towards a European consensus for reporting incidental findings during clinical NGS testing

Hehir-Kwa, Jayne Y ; Claustres, Mireille ; Hastings, Ros J ; van Ravenswaaij-Arts, Conny ; Christenhusz, Gabrielle ; Genuardi, Maurizio ; Melegh, Béla ; Cambon-Thomsen, Anne ; Patsalis, Philippos ; Vermeesch, Joris ; Cornel, Martina C ; Searle, Beverly ; Palotie, Aarno ; Capoluongo, Ettore ; Peterlin, Borut ; Estivill, Xavier ; Robinson, Peter N

European journal of human genetics : EJHG, 2015-12, Vol.23 (12), p.1601-1606 [Periódico revisado por pares]

England: Nature Publishing Group

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