检索结果 - Aarno Palotie

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  1. 1
    Use of population isolates for mapping complex traits

    Use of population isolates for mapping complex traits 由 Leena Peltonen, Aarno Palotie, Kenneth Lange

    出版 2000
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  2. 2
    A defect in the structure of type I procollagen in a patient who had osteogenesis imperfecta: excess mannose in the COOH-terminal propeptide.

    A defect in the structure of type I procollagen in a patient who had osteogenesis imperfecta: excess mannose in the COOH-terminal propeptide. 由 Leena Peltonen, Aarno Palotie, Darwin J. Prockop

    出版 1980
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  3. 3
    Lessons from studying monogenic disease for common disease

    Lessons from studying monogenic disease for common disease 由 Leena Peltonen, Markus Perola, Jussi Naukkarinen, Aarno Palotie

    出版 2006
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  4. 4
    Thermal stability of type I and type III procollagens from normal human fibroblasts and from a patient with osteogenesis imperfecta.

    Thermal stability of type I and type III procollagens from normal human fibroblasts and from a patient with osteogenesis imperfecta. 由 Leena Peltonen, Aarno Palotie, Toshihiko Hayashi, Darwin J. Prockop

    出版 1980
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  5. 5
    Systematic review of genome-wide expression studies in multiple sclerosis

    Systematic review of genome-wide expression studies in multiple sclerosis 由 A K Kemppinen, Jaakko Kaprio, Aarno Palotie, Janna Saarela

    出版 2011
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  6. 6
    Patterns of Inheritance of Constitutional Delay of Growth and Puberty in Families of Adolescent Girls and Boys Referred to Specialist Pediatric Care

    Patterns of Inheritance of Constitutional Delay of Growth and Puberty in Families of Adolescent Girls and Boys Referred to Specialist Pediatric Care 由 Karoliina Wehkalampi, Elisabeth Widén, Tiina Laine, Aarno Palotie, Leo Dunkel

    出版 2007
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  7. 7
    Genetic Risk Prediction and a 2-Stage Risk Screening Strategy for Coronary Heart Disease

    Genetic Risk Prediction and a 2-Stage Risk Screening Strategy for Coronary Heart Disease 由 Emmi Tikkanen, Aki S. Havulinna, Aarno Palotie, Veikko Salomaa, Samuli Ripatti

    出版 2013
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  8. 8
    Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder.

    Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder. 由 Helena Kuivaniemi, Leena Peltonen, Aarno Palotie, Ilkka Kaitila, Kari I. Kivirikko

    出版 1982
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  9. 9
    Tumor classification by tissue microarray profiling: random forest clustering applied to renal cell carcinoma

    Tumor classification by tissue microarray profiling: random forest clustering applied to renal cell carcinoma 由 Tao Shi, David B. Seligson, Arie S. Belldegrun, Aarno Palotie, Steve Horvath

    出版 2004
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  10. 10
    Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels

    Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels 由 Hanna Mikkola, Martti Syrjälä, Vesa Rasi, Elina Vahtera, Eija Hämäläinen, Leena Peltonen, Aarno Palotie

    出版 1994
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  11. 11
    Genomic Organization of Human and Mouse Genes for Vascular Endothelial Growth Factor C

    Genomic Organization of Human and Mouse Genes for Vascular Endothelial Growth Factor C 由 Dmitri Chilov, Eola Kukk, Suvi Taira, Michael Jeltsch, Jaakko Kaukonen, Aarno Palotie, Vladimir Joukov, Kari Alitalo

    出版 1997
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  12. 12
    Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in <i>MUC5B</i> mutation carriers

    Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in <i>MUC5B</i> mutation carriers 由 Antti Palomäki, Aarno Palotie, Jukka Koskela, Kari K. Eklund, Matti Pirinen, Samuli Ripatti, Tarja Laitinen, Nina Mars

    出版 2021
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  13. 13
    Systematic comparison of family history and polygenic risk across 24 common diseases

    Systematic comparison of family history and polygenic risk across 24 common diseases 由 Nina Mars, Joni V. Lindbohm, Pietro Della Briotta Parolo, Elisabeth Widén, Jaakko Kaprio, Aarno Palotie, Samuli Ripatti

    出版 2022
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  14. 14
    A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip® for Methylome Profiling

    A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip® for Methylome Profiling 由 Christine Clark, Priit Palta, Christopher J. Joyce, Carol Scott, Elin Grundberg, Panos Deloukas, Aarno Palotie, Alison J. Coffey

    出版 2012
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  15. 15
    Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16

    Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16 由 Kaisu Keskitalo, Antti Knaapila, Mikko Kallela, Aarno Palotie, Maija Wessman, Sampo Sammalisto, Leena Peltonen, Hely Tuorila, Markus Perola

    出版 2007
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  16. 16
    Tissue microarray analysis of cytoskeletal actin‐associated biomarkers gelsolin and E‐cadherin in urothelial carcinoma

    Tissue microarray analysis of cytoskeletal actin‐associated biomarkers gelsolin and E‐cadherin in urothelial carcinoma 由 Jianyu Rao, David B. Seligson, Harri Visapää, Steve Horvath, Mervi Eeva, Kia Michel, Allan Pantuck, Arie S. Belldegrun, Aarno Palotie

    出版 2002
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  17. 17
    Describing the genetic architecture of epilepsy through heritability analysis

    Describing the genetic architecture of epilepsy through heritability analysis 由 Doug Speed, Terence J. O’Brien, Aarno Palotie, Kirill Shkura, Anthony G Marson, David J. Balding, Michael R. Johnson

    出版 2014
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  18. 18
    Bmx Tyrosine Kinase Has a Redundant Function Downstream of Angiopoietin and Vascular Endothelial Growth Factor Receptors in Arterial Endothelium

    Bmx Tyrosine Kinase Has a Redundant Function Downstream of Angiopoietin and Vascular Endothelial Growth Factor Receptors in Arterial Endothelium 由 Iiro Rajantie, Niklas Ekman, Kristiina Iljin, Elena Arighi, Yuji Gunji, Jaakko Kaukonen, Aarno Palotie, Mieke Dewerchin, Peter Carmeliet, Kari Alitalo

    出版 2001
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  19. 19
    Neural, not gonadal, origin of brain sex differences in a gynandromorphic finch

    Neural, not gonadal, origin of brain sex differences in a gynandromorphic finch 由 Robert J. Agate, William Grisham, Juli Wade, Suzanne M. Mann, John C. Wingfield, Carolyn Schanen, Aarno Palotie, Arthur P. Arnold

    出版 2003
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  20. 20
    Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

    Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events 由 Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, Reetta Kälviäinen, Mark J. Daly

    出版 2024
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