Zobrazeno 1 - 10 of 31 pro vyhledávání: '"Noriko, Tonomura"'
5
Akademický článek
Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours.
Autor: Maja L Arendt, Malin Melin, Noriko Tonomura, Michele Koltookian, Celine Courtay-Cahen, Netty Flindall, Joyce Bass, Kim Boerkamp, Katherine Megquir, Lisa Youell, Sue Murphy, Colleen McCarthy, Cheryl London, Gerard R Rutteman, Mike Starkey, Kerstin Lindblad-Toh
Publikováno v: PLoS Genetics, Vol 11, Iss 11, p e1005647 (2015)
Canine mast cell tumours (CMCT) are one of the most common skin tumours in dogs with a major impact on canine health. Certain breeds have a higher risk of developing mast cell tumours, suggesting that underlying predisposing germ-line genetic factors
Externí odkaz: https://doaj.org/article/895b2898a7834518bb77388c3398301a
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6
Akademický článek
Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers.
Autor: Noriko Tonomura, Ingegerd Elvers, Rachael Thomas, Kate Megquier, Jason Turner-Maier, Cedric Howald, Aaron L Sarver, Ross Swofford, Aric M Frantz, Daisuke Ito, Evan Mauceli, Maja Arendt, Hyun Ji Noh, Michele Koltookian, Tara Biagi, Sarah Fryc, Christina Williams, Anne C Avery, Jong-Hyuk Kim, Lisa Barber, Kristine Burgess, Eric S Lander, Elinor K Karlsson, Chieko Azuma, Jaime F Modiano, Matthew Breen, Kerstin Lindblad-Toh
Publikováno v: PLoS Genetics, Vol 11, Iss 2, p e1004922 (2015)
Dogs, with their breed-determined limited genetic background, are great models of human disease including cancer. Canine B-cell lymphoma and hemangiosarcoma are both malignancies of the hematologic system that are clinically and histologically simila
Externí odkaz: https://doaj.org/article/5b00e49abada4f5abe8f6eab4d5205b1
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7
Akademický článek
Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24.
Autor: Caryline Agler, Dahlia M Nielsen, Ganokon Urkasemsin, Andrew Singleton, Noriko Tonomura, Snaevar Sigurdsson, Ruqi Tang, Keith Linder, Sampath Arepalli, Dena Hernandez, Kerstin Lindblad-Toh, Joyce van de Leemput, Alison Motsinger-Reif, Dennis P O'Brien, Jerold Bell, Tonya Harris, Steven Steinberg, Natasha J Olby
Publikováno v: PLoS Genetics, Vol 10, Iss 2, p e1003991 (2014)
Old English Sheepdogs and Gordon Setters suffer from a juvenile onset, autosomal recessive form of canine hereditary ataxia primarily affecting the Purkinje neuron of the cerebellar cortex. The clinical and histological characteristics are analogous
Externí odkaz: https://doaj.org/article/15e6ade6db1341d086f098b0a5fbf24c
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8
Akademický článek
Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis.
Autor: Mia Olsson, Linda Tintle, Marcin Kierczak, Michele Perloski, Noriko Tonomura, Andrew Lundquist, Eva Murén, Max Fels, Katarina Tengvall, Gerli Pielberg, Caroline Dufaure de Citres, Laetitia Dorso, Jérôme Abadie, Jeanette Hanson, Anne Thomas, Peter Leegwater, Åke Hedhammar, Kerstin Lindblad-Toh, Jennifer R S Meadows
Publikováno v: PLoS ONE, Vol 8, Iss 10, p e75242 (2013)
Autoinflammatory disease (AID) manifests from the dysregulation of the innate immune system and is characterised by systemic and persistent inflammation. Clinical heterogeneity leads to patients presenting with one or a spectrum of phenotypic signs,
Externí odkaz: https://doaj.org/article/55baf306337e4da0b85824b50133aec7
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9
Akademický článek
A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs.
Autor: Mia Olsson, Jennifer R S Meadows, Katarina Truvé, Gerli Rosengren Pielberg, Francesca Puppo, Evan Mauceli, Javier Quilez, Noriko Tonomura, Giordana Zanna, Maria José Docampo, Anna Bassols, Anne C Avery, Elinor K Karlsson, Anne Thomas, Daniel L Kastner, Erik Bongcam-Rudloff, Matthew T Webster, Armand Sanchez, Ake Hedhammar, Elaine F Remmers, Leif Andersson, Lluis Ferrer, Linda Tintle, Kerstin Lindblad-Toh
Publikováno v: PLoS Genetics, Vol 7, Iss 3, p e1001332 (2011)
Hereditary periodic fever syndromes are characterized by recurrent episodes of fever and inflammation with no known pathogenic or autoimmune cause. In humans, several genes have been implicated in this group of diseases, but the majority of cases rem
Externí odkaz: https://doaj.org/article/0fc34a2c6193493c831dd107ce05bb30
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