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40 résultats

	Pour les 40 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page : Page précédente 1 2 Page suivante	triés par Pertinence Auteur A→Z Auteur Z→A Titre A→Z Titre Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante

		A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys M. Abitbol , R. Legrand , Laurent L. Tiret Animal Genetics, 2014, 45 (6), pp.878-880. ⟨10.1111/age.12207⟩ Article dans une revue istex hal-02484632v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Prospective echocardiographic and tissue Doppler screening of a large Sphynx cat population: Reference ranges, heart disease prevalence and genetic aspects Valérie Chetboul , Amandine Petit , Vassiliki Gouni , Emilie Trehiou-Sechi , Charlotte Misbach , et al. Journal of Veterinary Cardiology, 2012, 14 (4), pp.497-509. ⟨10.1016/j.jvc.2012.08.001⟩ Article dans une revue istex hal-02484640v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Clinical characterisation of polydactyly in Maine Coon cats Alexia Hamelin , Dominique Begon , Fabrice Conchou , Marion Fusellier , Marie Abitbol Journal of Feline Medicine and Surgery, 2016, 19 (4), pp.382-393. ⟨10.1177/1098612X16628920⟩ Article dans une revue hal-02484743v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Les tests génétiques chez le chien Marie Abitbol , Catherine André , Guillaume Queney , Gilles Chaudieu Revue Francophone des Laboratoires, 2010, 2010 (420), pp.69-82. ⟨10.1016/S1773-035X(10)70422-6⟩ Article dans une revue istex hal-01117459v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats ( Felis catus ) L. Lyons , R. Buckley , R. Harvey , Marie Abitbol , Danielle Aberdein , et al. Animal Genetics, 2021, 52 (3), pp.321-332. ⟨10.1111/age.13059⟩ Article dans une revue hal-03237807v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesis Alireza Ghasemizadeh , Emilie Christin , Alexandre Guiraud , Nathalie Couturier , Marie Abitbol , et al. eLife, 2021, 10, ⟨10.7554/eLife.70490⟩ Article dans une revue hal-03370800v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Ursodesoxycholic acid and heme-arginate are unable to improve hematopoiesis and liver injury in an erythropoietic protoporphyria mouse model. M. Abitbol , H. Puy , J-M Sabaté , J-L Guénet , J-Ch Deybach , et al. Physiological Research, 2006, 55 Suppl 2, pp.S93-101 Article dans une revue hal-02484673v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Prevalence of deafness and association with coat variations in client-owned ferrets Stéphanie Piazza , Marie Abitbol , Kirsten Gnirs , Minh Huynh , Laurent Cauzinille Journal of the American Veterinary Medical Association, 2014, 244 (9), pp.1047-1052. ⟨10.2460/javma.244.9.1047⟩ Article dans une revue hal-02484638v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Feline chimerism revealed by DNA profiling Ambre Jaraud , Philippe Bossé , Caroline Dufaure de Citres , Laurent Tiret , Vincent Gache , et al. Animal Genetics, 2020, 51 (4), pp.631-633. ⟨10.1111/age.12957⟩ Article dans une revue hal-02888647v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Cataracts in a population of Bengal cats in France Aurélie Bourguet , Gilles Chaudieu , Alice Briatta , Alexandre Guyonnet , Marie Abitbol , et al. Veterinary Ophthalmology, 2018, 21 (1), pp.10-18. ⟨10.1111/vop.12470⟩ Article dans une revue hal-02484613v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Golden cats: A never‐ending story! Marie Abitbol , Tanushri Dargar , Vincent Gache Animal Genetics, 2022, 53 (5), pp.715-718. ⟨10.1111/age.13228⟩ Article dans une revue hal-04500600v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Breeding strategies against genetic disorders in dog breeds Grégoire Leroy , Marie Abitbol 9. World Congress on Genetics Applied to Livestock Production, Aug 2010, Leipzig, Germany Communication dans un congrès hal-01193344v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Dépistage génétique Marie Abitbol , Catherine André , Anne Thomas Affections oculaires héréditaires ou à prédisposition raciale chez le chien, 2013 Chapitre d'ouvrage hal-02484702v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys Marie Abitbol , Romain Legrand , Laurent Tiret Genetics Selection Evolution, 2015, 47 (1), ⟨10.1186/s12711-015-0112-x⟩ Article dans une revue hal-02484628v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys Romain Legrand , Laurent Tiret , Marie Abitbol Genetics Selection Evolution, 2014, 46 (1), ⟨10.1186/s12711-014-0065-5⟩ Article dans une revue hal-02484634v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Copal, a new MC 1R allele in the domestic cat Marie Abitbol , Vincent Gache Animal Genetics, 2019, 50 (5), pp.553-554. ⟨10.1111/age.12829⟩ Article dans une revue hal-02484609v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Prevalence of the MYBPC3-A31P mutation in a large European feline population and association with hypertrophic cardiomyopathy in the Maine Coon breed Jérôme Mary , Valérie Chetboul , Carolina Carlos Sampedrano , Marie Abitbol , Vassiliki Gouni , et al. Journal of Veterinary Cardiology, 2010, 12 (3), pp.155-161. ⟨10.1016/j.jvc.2010.06.004⟩ Article dans une revue istex hal-02484652v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis. Marie Abitbol , Jean-Laurent Thibaud , Natasha J. Olby , Christophe Hitte , Jean-Philippe Puech , et al. Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (33), pp.14775-80. ⟨10.1073/pnas.0914206107⟩ Article dans une revue inserm-00511951v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Donskoy cats as a new model of oculocutaneous albinism with the identification of a splice-site variant in Hermansky-Pudlak Syndrome 5 gene Marina Mériot , Christophe Hitte , Maud Rimbault , Caroline Dufaure de Citres , Vincent Gache , et al. Pigment Cell and Melanoma Research, 2020, 33 (6), pp.814-825. ⟨10.1111/pcmr.12906⟩ Article dans une revue hal-02888602v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats Marie Abitbol , Philippe Bossé , Anne Thomas , Laurent Tiret PLoS ONE, 2015, 10 (3), pp.e0120668. ⟨10.1371/journal.pone.0120668⟩ Article dans une revue hal-02484630v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Golden cats: The story goes on Marie Abitbol , Tanushri Dargar , Vincent Gache Animal Genetics, 2022, 53 (4), pp.543-545. ⟨10.1111/age.13215⟩ Article dans une revue hal-04500644v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		La céroïde-lipofuscinose de l'Américain Staffordshire Terrier Marie Abitbol Bulletin de l'Académie Vétérinaire de France, 2011, 164 (2), pp.113-118 Article dans une revue hal-02649115v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Genetic heterogeneity of polydactyly in Maine Coon cats Alexia Hamelin , Fabrice Conchou , Marion Fusellier , Bettina Duchenij , Isabelle Vieira , et al. Journal of Feline Medicine and Surgery, 2020, pp.1098612X2090506. ⟨10.1177/1098612X20905061⟩ Article dans une revue hal-02484604v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis M. Abitbol , J.-L. Thibaud , N. Olby , C. Hitte , J.-P. Puech , et al. Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (33), pp.14775-14780. ⟨10.1073/pnas.0914206107⟩ Article dans une revue hal-02484655v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A CDH23 missense variant in Beauceron dogs with non-syndromic deafness Marie Abitbol , Vidhya Jagannathan , Marie Lopez , Ambre Courtin , Caroline Dufaure de Citres , et al. Animal Genetics, 2022, ⟨10.1111/age.13273⟩ Article dans une revue hal-03854349v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia Marie Abitbol , Vidhya Jagannathan , Nelly Laurent , Eglantine Noblet , Guillaume Dutil , et al. Animal Genetics, 2022, 53 (5), pp.709-712. ⟨10.1111/age.13245⟩ Article dans une revue hal-04472411v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Allelic heterogeneity of albinism in the domestic cat Marie Abitbol , Philippe Bossé , Bénédicte Grimard , Lionel Martignat , Laurent Tiret Animal Genetics, 2017, 48 (1), pp.127-128. ⟨10.1111/age.12503⟩ Article dans une revue hal-02484616v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys Romain Legrand , Laurent Tiret , Marie Abitbol Genetics Selection Evolution, 2014, 46 (1), pp.65. ⟨10.1186/s12711-014-0065-5⟩ Article dans une revue hal-01341233v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys Marie Abitbol , Romain Legrand , Laurent Tiret Genetics Selection Evolution, 2015, 47 (1), pp.28. ⟨10.1186/s12711-015-0112-x⟩ Article dans une revue hal-01299594v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		A mouse model provides evidence that genetic background modulates anemia and liver injury in erythropoietic protoporphyria Marie Abitbol , Florence Bernex , Hervé Puy , Hélène Jouault , Jean-Charles Deybach , et al. AJP - Gastrointestinal and Liver Physiology, 2005, 288 (6), pp.G1208-G1216. ⟨10.1152/ajpgi.00505.2004⟩ Article dans une revue hal-02484682v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

Filtrer vos résultats

A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys

Prospective echocardiographic and tissue Doppler screening of a large Sphynx cat population: Reference ranges, heart disease prevalence and genetic aspects

Clinical characterisation of polydactyly in Maine Coon cats

Les tests génétiques chez le chien

Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats ( Felis catus )

MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesis

Ursodesoxycholic acid and heme-arginate are unable to improve hematopoiesis and liver injury in an erythropoietic protoporphyria mouse model.

Prevalence of deafness and association with coat variations in client-owned ferrets

Feline chimerism revealed by DNA profiling

Cataracts in a population of Bengal cats in France

Golden cats: A never‐ending story!

Breeding strategies against genetic disorders in dog breeds

Dépistage génétique

A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys

Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys

Copal, a new MC 1R allele in the domestic cat

Prevalence of the MYBPC3-A31P mutation in a large European feline population and association with hypertrophic cardiomyopathy in the Maine Coon breed

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.

Donskoy cats as a new model of oculocutaneous albinism with the identification of a splice-site variant in Hermansky-Pudlak Syndrome 5 gene

A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats

Golden cats: The story goes on

La céroïde-lipofuscinose de l'Américain Staffordshire Terrier

Genetic heterogeneity of polydactyly in Maine Coon cats

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis

A CDH23 missense variant in Beauceron dogs with non-syndromic deafness

A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia

Allelic heterogeneity of albinism in the domestic cat

Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys

A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys

A mouse model provides evidence that genetic background modulates anemia and liver injury in erythropoietic protoporphyria