Hasil Pencarian - Anu K. Lappalainen

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  1. 1
    Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10.

    Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10. oleh Kaisa Kyöstilä, Anu K Lappalainen, Hannes Lohi

    Diterbitkan 2013-01-01
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  2. 2
    Reliability of a New Bite Force Measure and Biomechanics of Modified Long Attack in Police Dogs

    Reliability of a New Bite Force Measure and Biomechanics of Modified Long Attack in Police Dogs oleh Heli K. Hyytiäinen, Laura Blomvall, Mikko Hautala, Anu K. Lappalainen

    Diterbitkan 2021-03-01
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  3. 3
    Persistent fontanelles in Chihuahuas. Part II: Association with craniocervical junction abnormalities, syringomyelia, and ventricular volume

    Persistent fontanelles in Chihuahuas. Part II: Association with craniocervical junction abnormalities, syringomyelia, and ventricular volume oleh Anna‐Mariam Kiviranta, Clare Rusbridge, Anu K. Lappalainen, Jouni J. T. Junnila, Tarja S. Jokinen

    Diterbitkan 2021-07-01
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  4. 4
    Persistent fontanelles in Chihuahuas. Part I. Distribution and clinical relevance

    Persistent fontanelles in Chihuahuas. Part I. Distribution and clinical relevance oleh Anna‐Mariam Kiviranta, Clare Rusbridge, Anu K. Lappalainen, Jouni J. T. Junnila, Tarja S. Jokinen

    Diterbitkan 2021-07-01
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  5. 5
    Polycythemia in dogs with chronic hypoxic pulmonary disease

    Polycythemia in dogs with chronic hypoxic pulmonary disease oleh Saila Holopainen, Henna P. Laurila, Anu K. Lappalainen, Minna M. Rajamäki, Sanna J. Viitanen

    Diterbitkan 2022-07-01
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  6. 6
    Breed-typical front limb angular deformity is associated with clinical findings in three chondrodysplastic dog breeds

    Breed-typical front limb angular deformity is associated with clinical findings in three chondrodysplastic dog breeds oleh Anu K. Lappalainen, Hanna S. M. Pulkkinen, Sari Mölsä, Jouni Junnila, Heli K. Hyytiäinen, Outi Laitinen-Vapaavuori

    Diterbitkan 2023-01-01
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  7. 7
    An across-breed validation study of 46 genetic markers in canine hip dysplasia

    An across-breed validation study of 46 genetic markers in canine hip dysplasia oleh Lea Mikkola, Kaisa Kyöstilä, Jonas Donner, Anu K. Lappalainen, Marjo K. Hytönen, Hannes Lohi, Antti Iivanainen

    Diterbitkan 2021-01-01
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  8. 8
    A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII.

    A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII. oleh Marjo K Hytönen, Meharji Arumilli, Anu K Lappalainen, Heli Kallio, Marjatta Snellman, Kirsi Sainio, Hannes Lohi

    Diterbitkan 2012-01-01
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  9. 9
    Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci

    Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci oleh Lea Mikkola, Saila Holopainen, Tiina Pessa-Morikawa, Anu K. Lappalainen, Marjo K. Hytönen, Hannes Lohi, Antti Iivanainen

    Diterbitkan 2019-12-01
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  10. 10
    Novel protective and risk loci in hip dysplasia in German Shepherds.

    Novel protective and risk loci in hip dysplasia in German Shepherds. oleh Lea I Mikkola, Saila Holopainen, Anu K Lappalainen, Tiina Pessa-Morikawa, Thomas J P Augustine, Meharji Arumilli, Marjo K Hytönen, Osmo Hakosalo, Hannes Lohi, Antti Iivanainen

    Diterbitkan 2019-07-01
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  11. 11
    Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.

    Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes. oleh Marjo K Hytönen, Meharji Arumilli, Anu K Lappalainen, Marta Owczarek-Lipska, Vidhya Jagannathan, Sruthi Hundi, Elina Salmela, Patrick Venta, Eva Sarkiala, Tarja Jokinen, Daniela Gorgas, Juha Kere, Pekka Nieminen, Cord Drögemüller, Hannes Lohi

    Diterbitkan 2016-05-01
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  12. 12
    A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease.

    A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. oleh Kaisa Kyöstilä, Pernilla Syrjä, Vidhya Jagannathan, Gayathri Chandrasekar, Tarja S Jokinen, Eija H Seppälä, Doreen Becker, Michaela Drögemüller, Elisabeth Dietschi, Cord Drögemüller, Johann Lang, Frank Steffen, Cecilia Rohdin, Karin H Jäderlund, Anu K Lappalainen, Kerstin Hahn, Peter Wohlsein, Wolfgang Baumgärtner, Diana Henke, Anna Oevermann, Juha Kere, Hannes Lohi, Tosso Leeb

    Diterbitkan 2015-04-01
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