Результаты поиска - Mikael Oscarson

  • Отображение 1 - 9 результаты of 9
Отмена результатов
  1. 1
    Isolated 46,XY Gonadal Dysgenesis in Two Sisters Caused by a Xp21.2 Interstitial Duplication Containing the<i>DAX1</i>Gene

    Isolated 46,XY Gonadal Dysgenesis in Two Sisters Caused by a Xp21.2 Interstitial Duplication Containing the<i>DAX1</i>Gene по Michela Barbaro, Mikael Oscarson, Jacqueline Schoumans, Johan Staaf, Sten A. Ivarsson, Anna Wedell

    Опубликовано 2007
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  2. 2
    Cytochrome P450 1B1 gene polymorphisms and postmenopausal breast cancer risk

    Cytochrome P450 1B1 gene polymorphisms and postmenopausal breast cancer risk по Tove Rylander‐Rudqvist, Sara Wedrén, Fredrik Granath, Keith Humphreys, Susanne Ahlberg, Elisabete Weiderpass, Mikael Oscarson, Magnus Ingelman‐Sundberg, Ingemar Persson

    Опубликовано 2003
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  3. 3
    Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA

    Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA по Michela Barbaro, Antonio Balsamo, Britt Marie Anderlid, Anne Grethe Myhre, Monia Gennari, Annalisa Nicoletti, Maria Carla Pittalis, Mikael Oscarson, Anna Wedell

    Опубликовано 2009
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  4. 4
    Genetic polymorphisms of cytochrome P450 2A6 in a case-control study on lung cancer in a French population.

    Genetic polymorphisms of cytochrome P450 2A6 in a case-control study on lung cancer in a French population. по Marie‐Anne Loriot, Sandra Rebuissou, Mikael Oscarson, Sylvie Cénée, Masami Miyamoto, Noritaka Ariyoshi, Tetsuya Kamataki, Denis Hémon, Philippe Beaune, Isabelle Stücker

    Опубликовано 2001
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  5. 5
    Characterization of a novelCYP2A7/CYP2A6 hybrid allele (CYP2A6*12) that causes reduced CYP2A6 activity

    Characterization of a novelCYP2A7/CYP2A6 hybrid allele (CYP2A6*12) that causes reduced CYP2A6 activity по Mikael Oscarson, Roman A. McLellan, Vendela Asp, MariCarmen Ledesma, María Luisa Bernal Ruiz, B. Sinués, Arja Rautio, Magnus Ingelman‐Sundberg

    Опубликовано 2002
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  6. 6
    Identification and characterisation of novel polymorphisms in the <i>CYP2A</i> locus: implications for nicotine metabolism

    Identification and characterisation of novel polymorphisms in the <i>CYP2A</i> locus: implications for nicotine metabolism по Mikael Oscarson, Roman A. McLellan, Harriet Gullstén, José A. G. Agúndez, Julio Benı́tez, Arja Rautio, Hannu Raunio, Olavi Pelkonen, Magnus Ingelman‐Sundberg

    Опубликовано 1999
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  7. 7
    Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1

    Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1 по Sophie Bensing, Sergueı̈ O. Fetissov, Jan Mulder, Jaakko Perheentupa, Jan Gustafsson, Eystein S. Husebye, Mikael Oscarson, Olov Ekwall, Patricia Crock, Tomas Hökfelt, Anna‐Lena Hulting, Olle Kämpe

    Опубликовано 2007
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  8. 8
    PARKIN is not required to sustain OXPHOS function in adult mammalian tissues

    PARKIN is not required to sustain OXPHOS function in adult mammalian tissues по Roberta Filograna, Jule Gerlach, Hae-Na Choi, Giovanni Rigoni, Michela Barbaro, Mikael Oscarson, Seungmin Lee, Katarína Tiklová, Markus Ringnér, Camilla Koolmeister, Rolf Wibom, Sara Riggare, Inger Nennesmo, Thomas Perlmann, Anna Wredenberg, Anna Wedell, Elisa Motori, Per Svenningsson, Nils‐Göran Larsson

    Опубликовано 2024
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  9. 9
    Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

    Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients по Henrik Stranneheim, Kristina Lagerstedt‐Robinson, Måns Magnusson, Malin Kvarnung, Daniel Nilsson, Nicole Lesko, Martin Engvall, Britt‐Marie Anderlid, Henrik Arnell, Carolina Backman Johansson, Michela Barbaro, Erik Björck, Helene Bruhn, Jesper Eisfeldt, Christoph Freyer, Giedre Grigelioniené, Peter Gustavsson, Anna Hammarsjö, Maritta Hellström-Pigg, Erik Iwarsson, Anders Jemt, Mikael Laaksonen, Sara Lind Enoksson, Helena Malmgren, K Naess, Magnus Nordenskjöld, Mikael Oscarson, Maria Pettersson, Chiara Rasi, Adam Rosenbaum, Ellika Sahlin, Eliane Sardh, Tommy Stödberg, Bianca Tesi, Emma Tham, Håkan Thonberg, Virpi Töhönen, Ulrika von Döbeln, Daphne Vassiliou, Sofie Vonlanthen, Ann–Charlotte Wikström, Josephine Wincent, Ola Winqvist, Anna Wredenberg, Sofia Ygberg, Rolf Zetterström, Per Marits, Maria Soller, Ann Nordgren, Valtteri Wirta, Anna Lindstrand, Anna Wedell

    Опубликовано 2021
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:

Инструменты поиска: