Resultados de procura - Virpi Launonen

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  1. 1
    Mutations in the human<i>LKB1/STK11</i>gene

    Mutations in the human<i>LKB1/STK11</i>gene por Virpi Launonen

    Publicado 2005
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  2. 2
    The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency

    The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency por Jean‐Pierre Bayley, Virpi Launonen, Ian Tomlinson

    Publicado 2008
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  3. 3
    Mutation analysis of the CHK2gene in families with hereditary breast cancer

    Mutation analysis of the CHK2gene in families with hereditary breast cancer por Minna Allinen, Pia Huusko, Samu Mäntyniemi, Virpi Launonen, Robert Winqvist

    Publicado 2001
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  4. 4
    Analysis of fumarate hydratase mutations in a population‐based series of early onset uterine leiomyosarcoma patients

    Analysis of fumarate hydratase mutations in a population‐based series of early onset uterine leiomyosarcoma patients por Sanna K. Ylisaukko‐oja, Maija Kiuru, Heli Lehtonen, Rainer Lehtonen, ­Eero Pukkala, Johanna Arola, Virpi Launonen, Lauri A. Aaltonen

    Publicado 2006
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  5. 5
    Inherited susceptibility to uterine leiomyomas and renal cell cancer

    Inherited susceptibility to uterine leiomyomas and renal cell cancer por Virpi Launonen, Outi Vierimaa, Maija Kiuru, Jorma Isola, Stina Roth, ­Eero Pukkala, Pertti Sistonen, Riitta Herva, Lauri A. Aaltonen

    Publicado 2001
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  6. 6
    Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

    Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families por Pia Huusko, Kati Pääkkönen, Virpi Launonen, Minna Pöyhönen, Guillermo Blanco, Antti Kauppila, Ulla Puistola, Heikki Kiviniemi, Marika Kujala, Jaakko Leisti, Robert Winqvist

    Publicado 1998
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  7. 7
    Induction of cyclooxygenase-2 in a mouse model of Peutz–Jeghers polyposis

    Induction of cyclooxygenase-2 in a mouse model of Peutz–Jeghers polyposis por Derrick J. Rossi, Antti Ylikorkala, Nina Korsisaari, Reijo Salovaara, Keijo Luukko, Virpi Launonen, Mark Henkemeyer, Ari Ristimäki, Lauri A. Aaltonen, Tomi P. Mäkelä

    Publicado 2002
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  8. 8
    Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

    Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology por Maija Kiuru, Virpi Launonen, Marja Hietala, Kristiina Aittomäki, Outi Vierimaa, Reijo Salovaara, Johanna Arola, ­Eero Pukkala, Pertti Sistonen, Riitta Herva, Lauri A. Aaltonen

    Publicado 2001
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  9. 9
    Frequent loss of SMAD4/DPC4 protein in colorectal cancers

    Frequent loss of SMAD4/DPC4 protein in colorectal cancers por Reijo Salovaara, Stephan Roth, Anu Loukola, Virpi Launonen, P. Sistonen, Egle Avizienyte, Paula Kristo, Heikki Järvinen, Serhiy Souchelnytskyi, Maarit Sarlomo‐Rikala, Lauri A. Aaltonen

    Publicado 2002
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  10. 10
    The Expression of AIP-Related Molecules in Elucidation of Cellular Pathways in Pituitary Adenomas

    The Expression of AIP-Related Molecules in Elucidation of Cellular Pathways in Pituitary Adenomas por Elina Heliövaara, Anniina Raitila, Virpi Launonen, Anders Paetau, Johanna Arola, Heli Lehtonen, Timo Sane, Robert J. Weil, Outi Vierimaa, Pasi Salmela, Karoliina Tuppurainen, Markus J. Mäkinen, Lauri A. Aaltonen, Auli Karhu

    Publicado 2009
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  11. 11
    <i>MED12</i> , the <i>Mediator Complex Subunit 12</i> Gene, Is Mutated at High Frequency in Uterine Leiomyomas

    <i>MED12</i> , the <i>Mediator Complex Subunit 12</i> Gene, Is Mutated at High Frequency in Uterine Leiomyomas por Netta Mäkinen, Miika Mehine, Jaana Tolvanen, Eevi Kaasinen, Yilong Li, Heli Lehtonen, Massimiliano Gentile, Jian Yan, Martin Enge, Minna Taipale, Mervi Aavikko, Riku Katainen, Elina Virolainen, Tom Böhling, Taru A. Koski, Virpi Launonen, Jari Sjöberg, Jussi Taipale, Pia Vahteristo, Lauri A. Aaltonen

    Publicado 2011
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  12. 12
    Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations

    Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations por Marianthi Georgitsi, Anniina Raitila, Auli Karhu, Karoliina Tuppurainen, Markus J. Mäkinen, Outi Vierimaa, Ralf Paschke, Wolfgang Saeger, Rob B. van der Luijt, Timo Sane, Mercedes Robledo, Ernesto De Menis, Robert J. Weil, A. Wasik, Grzegorz Zieliński, Olga Lucewicz, Jan Lubiński, Virpi Launonen, Pia Vahteristo, Lauri A. Aaltonen

    Publicado 2007
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  13. 13
    Mutations in the Circadian Gene <i>CLOCK</i> in Colorectal Cancer

    Mutations in the Circadian Gene <i>CLOCK</i> in Colorectal Cancer por Pia Alhopuro, Mikael Björklund, Heli Sammalkorpi, Mikko Turunen, Sari Tuupanen, Mia Biström, Iina Niittymäki, Heli Lehtonen, Teemu Kivioja, Virpi Launonen, Juha Saharinen, Kari Nousiainen, Sampsa Hautaniemi, Kyösti Nuorva, Jukka‐Pekka Mecklin, Heikki Järvinen, Torben Ørntoft, Diego Arango, Rainer Lehtonen, Auli Karhu, Jussi Taipale, Lauri A. Aaltonen

    Publicado 2010
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  14. 14
    Biallelic Inactivation of Fumarate Hydratase (FH) Occurs in Nonsyndromic Uterine Leiomyomas but Is Rare in Other Tumors

    Biallelic Inactivation of Fumarate Hydratase (FH) Occurs in Nonsyndromic Uterine Leiomyomas but Is Rare in Other Tumors por Rainer Lehtonen, Maija Kiuru, Sakari Vanharanta, Jari Sjöberg, Leena‐Maija Aaltonen, Kristiina Aittomäki, Johanna Arola, Ralf Bützow, Charis Eng, Kirsti Husgafvel‐Pursiainen, Jorma Isola, Heikki Järvinen, Pasi A. Koivisto, Jukka‐Pekka Mecklin, Païvi Peltomäki, Reijo Salovaara, Veli-Matti Wasenius, Auli Karhu, Virpi Launonen, Nina N. Nupponen, Lauri A. Aaltonen

    Publicado 2004
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  15. 15
    Unregulated smooth-muscle myosin in human intestinal neoplasia

    Unregulated smooth-muscle myosin in human intestinal neoplasia por Pia Alhopuro, Denis Phichith, Sari Tuupanen, Heli Sammalkorpi, Miranda Nybondas, Juha Saharinen, James P. Robinson, Zhaohui Yang, Li-Qiong Chen, Torben Ørntoft, Jukka‐Pekka Mecklin, Heikki Järvinen, Charis Eng, Gabriela Möslein, Darryl Shibata, Richard S. Houlston, Anneke Lucassen, Ian Tomlinson, Virpi Launonen, Ari Ristimäki, Diego Arango, Auli Karhu, H. Lee Sweeney, Lauri A. Aaltonen

    Publicado 2008
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  16. 16
    Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland

    Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland por Laura Sarantaus, Pia Huusko, Hannaleena Eerola, Virpi Launonen, Paula Vehmanen, Katrin Rapakko, Elizabeth M. Gillanders, Kirsi Syrjäkoski, Tommi Kainu, Pia Vahteristo, Ralf Krahe, Kati Pääkkönen, Jaana M. Hartikainen, Carl Blomqvist, Tuija Löppönen, Kaija Holli, Markku Ryynänen, Ralf Bützow, Åke Borg, Brita Arver, Eva Holmberg, Graham J. Mann, Juha Kere, Olli Kallioniemi, Robert Winqvist, Heli Nevanlinna

    Publicado 2000
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  17. 17
    Germline CDKN1B/p27Kip1 Mutation in Multiple Endocrine Neoplasia

    Germline CDKN1B/p27Kip1 Mutation in Multiple Endocrine Neoplasia por Marianthi Georgitsi, Anniina Raitila, Auli Karhu, Rob B. van der Luijt, Cora M. Aalfs, Timo Sane, Outi Vierimaa, Markus J. Mäkinen, Karoliina Tuppurainen, R Paschke, Oliver Gimm, Christian A. Koch, Sadi Gündoğdu, Anneke Lucassen, Marc Tischkowitz, Louise Izatt, Simon Aylwin, Gul Bano, Shirley Hodgson, Ernesto De Menis, Virpi Launonen, Pia Vahteristo, Lauri A. Aaltonen

    Publicado 2007
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  18. 18
    Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes*

    Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes* por Xiaoping Zhou, K Woodford-Richens, Rainer Lehtonen, Keisuke Kurose, Micheala A. Aldred, Heather Hampel, Virpi Launonen, Sanno Virta, Robert Pilarski, Reijo Salovaara, Walter F. Bodmer, Beth A. Conrad, Malcolm G. Dunlop, Shirley V. Hodgson, Takeo Iwama∥, Heikki Järvinen, Ilmo Kellokumpu, J‐H Kim, Barbara Leggett, David Markie, Jukka‐Pekka Mecklin, Kay Neale, Robin Phillips, J Piris, Paul Rozen, Richard S. Houlston, Lauri A. Aaltonen, Ian Tomlinson, Charis Eng

    Publicado 2001
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  19. 19
    Expression Profiling in Progressive Stages of Fumarate-Hydratase Deficiency: The Contribution of Metabolic Changes to Tumorigenesis

    Expression Profiling in Progressive Stages of Fumarate-Hydratase Deficiency: The Contribution of Metabolic Changes to Tumorigenesis por Houman Ashrafian, Linda O′Flaherty, Julie Adam, Violetta Steeples, Yuen‐Li Chung, Philip East, Sakari Vanharanta, Heli Lehtonen, Emma Nye, Emine Hatipoglu, Melroy Miranda, Kimberley Howarth, Deepa Shukla, Helen Troy, John Griffiths, Bradley Spencer‐Dene, Mohammed Yusuf, Emanuela V. Volpi, Patrick H. Maxwell, Gordon Stamp, Richard Poulsom, Christopher W. Pugh, Barbara Costa, Chiara Bardella, Maria Flavia Di Renzo, Michael I. Kotlikoff, Virpi Launonen, Lauri A. Aaltonen, Mona El‐Bahrawy, Ian Tomlinson, Patrick J. Pollard

    Publicado 2010
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