المساهمون: Uludağ Üniversitesi/Tıp Fakültesi., Gülten, Tuna, Temel, Sehime, Evke, Elif, Cangül, Hakan, Yakut, Tahsin, AAG-8385-2021

مصطلحات موضوعية: Biochemistry & molecular biology, Genetics & heredity

العلاقة: Makale - Uluslararası Hakemli Dergi; Chromosome Research; Gülten, T. vd. (2007). "An azoospermic case with (16)(q22) fragile site". Chromosome Research, 15, Supplement 1, 47-47.; https://hdl.handle.net/11452/40104Test; 000248859800098; 47; 15

الإتاحة: https://hdl.handle.net/11452/40104Test

المؤلفون: Dean Gentle, Hans-Christoph Rossbach, Carlos Dalence, Richard C. Trembath, Anna Straatman-Iwanowska, Nicholas J. Davies, Hakan Cangul, Eamonn R. Maher, Serdar Ceylaner, Peter Devilee, Paul Gissen, Mark R. Morris, Fatimah Rahman, Maaike P.G. Vreeswijk, David Tannahill, Margaret A. Knowles, Erol Kismet, Diane Gleeson, Vedat Koseoglu, Stephen Keenan, Neil V. Morgan, Shanaz Pasha

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Cangül, Hakan

المصدر: PLoS Genetics, 6(2)
PLoS Genetics, Vol 6, Iss 2, p e1000833 (2010)
PLoS Genetics
PLoS Genetics, 6 (2), Article e1000833. (2010)

مصطلحات موضوعية: Hypertrichosis, Pathology, Adenosine, Mouse, Lymphadenopathy, Apoptosis, Pathogenesis, Faisalabad histiocytosis, Embryo development, Gene, Animal embryo, Chromosome 10, Mice, Consanguinity, Breast cancer, 0302 clinical medicine, Cell proliferation, Gene expression regulation, 0303 health sciences, Physical chromosome mapping, RNA, small interfering, 3. Good health, Histiocytosis, 030220 oncology & carcinogenesis, HeLa cell, Human, Protein slc29a3, medicine.medical_specialty, Embryo, mammalian, Cells, Genetic loci, Urinary bladder neoplasms, Clinical article, SLC29A3 protein, Article, 03 medical and health sciences, Genetics, Humans, Cancer cell culture, Family, Chromosome 10q, Molecular Biology, Alleles, Gene mapping, Ecology, Evolution, Behavior and Systematics, Histiocyte, Animal, Chromosomes, human, pair 10, Tumor cell line, ENT3 protein, medicine.disease, Rosai Dorfman disease, Cell line, tumor, Human cell, Chromosome map, Mutation, Cell strain HEK293, Gene expression, Breast neoplasms, Nucleotide sequence, Cancer Research, Candidate gene, Unclassified drug, Growth, Gene locus, Colony-forming units assay, Animal tissue, DNA mutational analysis, adenosine induces apoptosis sensorineural deafness cells lymphadenopathy activation brothers pathway growth cancer hent3, Histiocytosis, sinus, Molecular genetics, Genetics and Genomics/Genetics of Disease, Genetics (clinical), Rosai–Dorfman disease, Allele, Genetics & heredity, Bladder cancer, Syndrome, Small interfering RNA, Phenotype, Embryo, Histiocytoses, Genetics and Genomics/Gene Discovery, Female, Research Article, lcsh:QH426-470, Breast tumor, ADENOSINE INDUCES APOPTOSIS, SENSORINEURAL DEAFNESS, CELLS, LYMPHADENOPATHY, ACTIVATION, BROTHERS, PATHWAY, GROWTH, CANCER, HENT3, Nucleoside transporter, Biology, Germline mutation, Molecular sequence data, Bladder tumor, medicine, Animals, Gene mutation, Sinus Histiocytosis, Emperipolesis, Sinus histiocytosis, 030304 developmental biology, Equilibrative nucleoside transporter 3, Nucleoside transport proteins, Clonogenic assay, Sinus Histiocytosis with Massive Lymphadenopathy, Carrier proteins and binding proteins, Mutational analysis, Nonhuman, Base sequence, Autosomal recessive inheritance, lcsh:Genetics, Metabolism, Clinical feature, Protein protein interaction, Equilibrative nucleoside transporter, Controlled study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3211d2c6698969a5cb20cd46c412a444Test
https://doi.org/10.1371/journal.pgen.1000833Test