Zobrazeno 1 - 10
of 34
pro vyhledávání: '"genetics, Phenotype"'
Autor:
Suwara, Marek
Publikováno v:
World Literature Studies. III(3):3-14
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=246996
Autor:
Choong, Carissa
This is the master thesis that Dr. Choong completed as a partial fulfillment of her pediatric dentistry residency training.
GENETICS OF SHORT ROOT ANOMALIES Purpose: The purpose of this study is to define clinical features and identify specific
GENETICS OF SHORT ROOT ANOMALIES Purpose: The purpose of this study is to define clinical features and identify specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b745197edecaf85601907cfef630a3cf
Autor:
Carleton, Stephanie M.
Publikováno v:
Freely available online.
Thesis (Ph.D.)--University of Missouri-Columbia, 2006.
The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical genera
The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical genera
Externí odkaz:
http://hdl.handle.net/10355/4474
Autor:
Fontanesi L.
This chapter compiles and updates the knowledge on morphological, physiological and biochemical traits under genetic control and on inherited disorders documented in the European rabbit. The chapter is also focused on the recent developments determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803f4f6b91749dc23e52a7e470fe71c9
https://doi.org/10.1079/9781780643342.0008
https://doi.org/10.1079/9781780643342.0008
Autor:
Elena Caldarazzo Ienco, Claudio Bruno, Massimiliano Filosto, Graziella Uziel, Maurizio Moggio, Daniele Orsucci, Enrico Bertini, Isabella Moroni, Gabriele Siciliano, Corrado Angelini, Paola Tonin, Mauro Scarpelli, Massimo Zeviani, Elena Pegoraro, Marco Spinazzi, M. Sciacco, Serenella Servidei, Liliana Vercelli, Diego Martinelli, Maria Lucia Valentino, Valerio Carelli, Carlo Minetti, Michelangelo Mancuso, Filippo M. Santorelli, Donato Sauchelli, Costanza Lamperti, Giacomo P. Comi, Tiziana Mongini, Dario Ronchi, Olimpia Musumeci, Antonio Toscano
Publikováno v:
Neurology. 80:2049-2054
Objectives: Myoclonic epilepsy with ragged-red fibers (MERRF) is a rare mitochondrial syndrome, mostly caused by the 8344A>G mitochondrial DNA mutation. Most of the previous studies have been based on single case/family reports or series with few pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19a976b6884917b002d2e1fa9986c1cd
https://doi.org/10.1212/wnl.0b013e318294b44c
https://doi.org/10.1212/wnl.0b013e318294b44c
Autor:
Alexander V. Kirichenko, Tatiana I. Axenovich, James F. Wilson, Alan F. Wright, Sarah H. Wild, Christian Pattaro, Sarah Knott, Ingvar Jonasson, Harry Campbell, Fabio Marroni, Andrew A. Hicks, Åsa Johansson, Veronique Vitart, Aaron Isaacs, Igor Rudan, Nicholas D. Hastie, Cornelia M. van Duijn, Yurii S. Aulchenko, Peter P. Pramstaller, Chris S. Franklin, Irina V. Zorkoltseva, Caroline Hayward, Ben A. Oostra, Ulf Gyllensten, Gordan Lauc, Irene Pichler, Krešimir Rotim, Jamie Floyd, Susan Campbell
Publikováno v:
ResearcherID
Obesity, 18(4), 803-808. Wiley-Blackwell
Obesity, 18(4), 803-808. Wiley-Blackwell
As major risk-factors for diabetes and cardiovascular diseases, the genetic contribution to obesity-related traits has been of interest for decades. Recently, a limited number of common genetic variants, which have replicated in different populations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f42c08f22b66dc14deca12ce91c8e1a
https://doi.org/10.1038/oby.2009.359
https://doi.org/10.1038/oby.2009.359
Autor:
Kostas Stamatopoulos, Elisa Sozzi, Nikos Darzentas, Graham Packham, Freda K. Stevenson, C. Ian Mockridge, Francesco Forconi, Isla Wheatley, Kathleen N. Potter
Publikováno v:
Blood. 115:71-77
The cell of origin of chronic lymphocytic leukemia (CLL) has long been sought, and immunoglobulin gene analysis provides new clues. In the unmutated subset (U-CLL), there is increased usage of the 51p1-related alleles of the immunoglobulin heavy chai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::280054ed9dca76782644ad46f18244a5
https://doi.org/10.1182/blood-2009-06-225813
https://doi.org/10.1182/blood-2009-06-225813
Autor:
Francesco Bertoni, Giorgio Inghirami, Emanuele Zucca, Valter Gattei, Francesco Forconi, Ivo Kwee, Michael Mian, Davide Rossi, Andrea Rinaldi, Clara Deambrogi, Silvia Rasi, Elisa Sozzi, Marta Scandurra, Michaela Cerri, Gianluca Gaidano, Paola M.V. Rancoita, Miguel A. Piris, Santiago Moreno, Ekaterina Chigrinova, Maurilio Ponzoni
Publikováno v:
Hematological Oncology. 28:62-67
Richter's syndrome (RS) represents the transformation of chronic lymphocytic leukaemia (CLL) to aggressive lymphoma and is mostly represented by diffuse large B-cell lymphoma (DLBCL), with a post-germinal centre (GC) phenotype, clonally related to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54b37991bb70a4e9e6a266312cc735bc
https://doi.org/10.1002/hon.932
https://doi.org/10.1002/hon.932
Autor:
Lucia Galli, Vincenzo Sorrentino, Alfredo Orrico, Sabrina Buoni, Alessandra Orsi, Giuseppina Vonella
Publikováno v:
Clinical Genetics. 75:195-198
Somatic mutations of the phosphatase and tensin (PTEN) gene have been frequently detected in many types of human cancer. However, germline mutations can determine multiple hamartoma syndromes and, as more recently ascertained, syndromes clinically ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3d13a0a6f5baff85756ef8dbc8c295d
https://doi.org/10.1111/j.1399-0004.2008.01074.x
https://doi.org/10.1111/j.1399-0004.2008.01074.x
Autor:
Laurent Keller
Publikováno v:
American Naturalist, vol. 169, no. 1, pp. 1-8
Important scientific findings frequently arise from serendipitous findings. Unfortunately, many scientists are not prepared to take advantage of unexpected results and to question established paradigms, and this prevents them from capitalizing on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e24bf832b54ca43bfd9cb4a38d7d098
https://doi.org/10.1086/509938
https://doi.org/10.1086/509938