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1دورية أكاديمية
المؤلفون: Morgan, Neil V., Morris, Mark R., Gleeson, Diane, Straatman-Iwanowska, Anna A., Davies, Nicholas James, Keenan, Stephen J., Pasha, Shanaz S., Rahman, Fatimah, Gentle, Dean C., Vreeswijk, Maaike P.G., Devilee, Peter, Knowles, Margaret A., Ceylaner, Serdar, Trembath, Richard C., Dalence, Carlos, Kısmet, Erol, Köseoğlu, Vedat, Rossbach, Hans Christoph, Gissen, Paul, Tannahill, David, Mäher, Eamonn Richard
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Cangül, Hakan, 8911611600
مصطلحات موضوعية: Adenosine, Lymphadenopathy, Apoptosis, Growth, Cells, Gene, Genetics & heredity, Alleles, Animals, Base sequence, Breast neoplasms, Cell line, tumor, Cell proliferation, Chromosomes, human, pair 10, Colony-forming units assay, DNA mutational analysis, Embryo, mammalian, Family, Female, Gene expression regulation, Genetic loci, Histiocytosis, sinus, Humans, Mice, Molecular sequence data
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; PLoS Genetics; Yurt içi; Yurt dışı; Sanayi; Morgan, N. V. vd. (2010). "Mutations in SLC29a3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease". PLoS Genetics, 6(2).; https://doi.org/10.1371/journal.pgen.1000833Test; https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1000833Test; http://hdl.handle.net/11452/28527Test; 000275262700029; 2-s2.0-77649196563
الإتاحة: https://doi.org/10.1371/journal.pgen.1000833Test
http://hdl.handle.net/11452/28527Test
https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1000833Test -
2دورية أكاديمية
المؤلفون: Morgan, Neil V., Morris, Mark R., Gleeson, Diane, Straatman-Iwanowska, Anna A., Davies, Nicholas James, Keenan, Stephen J., Pasha, Shanaz S., Rahman, Fatimah, Gentle, Dean C., Vreeswijk, Maaike P.G., Devilee, Peter, Knowles, Margaret A., Ceylaner, Serdar, Trembath, Richard C., Dalence, Carlos, Kısmet, Erol, Köseoğlu, Vedat, Rossbach, Hans Christoph, Gissen, Paul, Tannahill, David, Mäher, Eamonn Richard
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Cangül, Hakan, 8911611600
مصطلحات موضوعية: Adenosine, Lymphadenopathy, Apoptosis, Growth, Cells, Gene, Genetics & heredity, Alleles, Animals, Base sequence, Breast neoplasms, Cell line, tumor, Cell proliferation, Chromosomes, human, pair 10, Colony-forming units assay, DNA mutational analysis, Embryo, mammalian, Family, Female, Gene expression regulation, Genetic loci, Histiocytosis, sinus, Humans, Mice, Molecular sequence data
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; PLoS Genetics; Yurt içi; Yurt dışı; Sanayi; Morgan, N. V. vd. (2010). "Mutations in SLC29a3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease". PLoS Genetics, 6(2).; https://doi.org/10.1371/journal.pgen.1000833Test; https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1000833Test; http://hdl.handle.net/11452/28527Test; 000275262700029; 2-s2.0-77649196563
الإتاحة: https://doi.org/10.1371/journal.pgen.1000833Test
http://hdl.handle.net/11452/28527Test
https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1000833Test
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