Výsledky vyhledávání - "Maria K Johansson"

Akademický článek

The refractive state of the eye in Icelandic horses with the Silver mutation

Autor: Maria K. Johansson, Kim Jäderkvist Fegraeus, Gabriella Lindgren, Björn Ekesten

Publikováno v: BMC Veterinary Research, Vol 13, Iss 1, Pp 1-7 (2017)

Abstract Background The syndrome Multiple Congenital Ocular Anomalies (MCOA) is a congenital eye disorder in horses. Both the MCOA syndrome and the Silver coat colour in horses are caused by the same missense mutation in the premelanosome protein (PM

Externí odkaz: https://doaj.org/article/5c3d06bb971e432d98fbc062edb61852

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Akademický článek

Lack of significant associations with early career performance suggest no link between the DMRT3 'Gait Keeper' mutation and precocity in Coldblooded trotters.

Autor: Kim Jäderkvist Fegraeus, Chameli Lawrence, Katrine Petäjistö, Maria K Johansson, Maja Wiklund, Christina Olsson, Leif Andersson, Lisa S Andersson, Knut H Røed, Carl-Fredrik Ihler, Eric Strand, Gabriella Lindgren, Brandon D Velie

Publikováno v: PLoS ONE, Vol 12, Iss 5, p e0177351 (2017)

The Swedish-Norwegian Coldblooded trotter (CBT) is a local breed in Sweden and Norway mainly used for harness racing. Previous studies have shown that a mutation from cytosine (C) to adenine (A) in the doublesex and mab-3 related transcription factor

Externí odkaz: https://doaj.org/article/130ea0b46ded4962b1393dbbcc9b8f5d

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Akademický článek

Erratum to: The refractive state of the eye in Icelandic horses with the Silver mutation

Autor: Maria K. Johansson, Kim Jäderkvist Fegraeus, Gabriella Lindgren, Björn Ekesten

Publikováno v: BMC Veterinary Research, Vol 13, Iss 1, Pp 1-1 (2017)

Externí odkaz: https://doaj.org/article/d0a36b734f9a423eaa304843ddba0f89

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The refractive state of the eye in Icelandic horses with the Silver mutation

Autor: Maria K. Johansson, Kim Jäderkvist Fegraeus, Gabriella Lindgren, Björn Ekesten

Publikováno v: BMC Veterinary Research
BMC Veterinary Research, Vol 13, Iss 1, Pp 1-7 (2017)

Background The syndrome Multiple Congenital Ocular Anomalies (MCOA) is a congenital eye disorder in horses. Both the MCOA syndrome and the Silver coat colour in horses are caused by the same missense mutation in the premelanosome protein (PMEL) gene.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9f90b62cbb1fd6047662e0485133c5d5
https://pubmed.ncbi.nlm.nih.gov/28662651

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Hematopoietic stem cell-targeted neonatal gene therapy reverses lethally progressive osteopetrosis in oc/oc mice

Autor: Stefan Karlsson, Maria K. Johansson, Anders Fasth, Vincent Everts, Teun J. de Vries, Johan Richter, Ann C.M. Brun, Mats Ehinger, Ton Schoenmaker

Publikováno v: Johansson, M K, de Vries, T J, Schoenmaker, A M, Ehinger, M, Brun, A C, Fasth, A, Karlsson, S, Everts, V & Richter, J 2007, ' Hematopoietic stem cell-targeted neonatal gene therapy reverses lethally progressive osteopetrosis in oc/oc mice ', Blood, vol. 109, pp. 5178-5185 . https://doi.org/10.1182/blood-2006-12-061382
Blood, 109, 5178-5185. American Society of Hematology
Blood; 109(12), pp 5178-5185 (2007)

Infantile malignant osteopetrosis (IMO) is a fatal disease caused by lack of functional osteoclasts, and the only available treatment is hematopoietic stem cell (HSC) transplantation. In the majority of patients, the TCIRG1 gene, coding for a subunit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4d9092833a1d61cd4b0c261d9e7c81
https://doi.org/10.1182/blood-2006-12-061382

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