المؤلفون: Zhao J, Liu L, Lv S, Wang C, Yue H, Zhang Z

المصدر: Pharmacogenomics and Personalized Medicine, Vol Volume 14, Pp 1669-1678 (2021)

مصطلحات موضوعية: alendronate, bone mineral density, osteoporosis, pfn1 gene, single-nucleotide polymorphism, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

العلاقة: https://www.dovepress.comTest/pfn1-gene-polymorphisms-and-the-bone-mineral-density-response-to-alend-peer-reviewed-fulltext-article-PGPM; https://doaj.org/toc/1178-7066Test

الوصول الحر: https://doaj.org/article/cf5599d80ac04b209a12a4f3174cc0aaTest

المؤلفون: Jiao Zhao, Li Liu, Shanshan Lv, Chun Wang, Hua Yue, Zhenlin Zhang

المصدر: Pharmacogenomics and Personalized Medicine

مصطلحات موضوعية: Pharmacology, musculoskeletal diseases, Pharmacogenomics and Personalized Medicine, Molecular Medicine, alendronate, single-nucleotide polymorphism, bone mineral density, PFN1 gene, osteoporosis, Original Research

وصف الملف: text/html

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d85eb1684caacb94a3569817968cef3Test
http://europepmc.org/articles/PMC8711734Test

المؤلفون: Merlotti D., Materozzi M., Bianciardi S., Guarnieri V., Rendina D., Volterrani L., Bellan C., Mingiano C., Picchioni T., Frosali A., Orfanelli U., Cenci S., Gennari L.

المساهمون: Merlotti, D., Materozzi, M., Bianciardi, S., Guarnieri, V., Rendina, D., Volterrani, L., Bellan, C., Mingiano, C., Picchioni, T., Frosali, A., Orfanelli, U., Cenci, S., Gennari, L.

مصطلحات موضوعية: bisphosphonate, osteoclast, Paget disease of bone, PFN1 gene, whole exome sequencing

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32392277; info:eu-repo/semantics/altIdentifier/wos/WOS:000565927300067; volume:105; issue:8; firstpage:2553; lastpage:2565; numberofpages:13; journal:THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; http://hdl.handle.net/11365/1121728Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85086346663

الإتاحة: https://doi.org/10.1210/clinem/dgaa252Test
http://hdl.handle.net/11365/1121728Test

المؤلفون: Ugo Orfanelli, Domenico Rendina, Alessandro Frosali, Luigi Gennari, Tommaso Picchioni, Christian Mingiano, Cristiana Bellan, Vito Guarnieri, Maria Materozzi, Simone Bianciardi, Simone Cenci, Luca Volterrani, Daniela Merlotti

المساهمون: Merlotti, Daniela, Materozzi, Maria, Bianciardi, Simone, Guarnieri, Vito, Rendina, Domenico, Volterrani, Luca, Bellan, Cristiana, Mingiano, Cristian, Picchioni, Tommaso, Frosali, Alessandro, Orfanelli, Ugo, Cenci, Simone, Gennari, Luigi

مصطلحات موضوعية: bisphosphonate, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Clinical Biochemistry, Gene mutation, PFN1 gene, Severity of Illness Index, Biochemistry, Monocytes, whole exome sequencing, Profilins, Endocrinology, Osteogenesis, Age of Onset, Frameshift Mutation, Exome sequencing, Middle Aged, Pedigree, Mutation (genetic algorithm), osteoclast, Paget disease of bone, bisphosphonates, medicine.symptom, Adult, Heterozygote, medicine.medical_specialty, Adolescent, Primary Cell Culture, Context (language use), macromolecular substances, Biology, Bone and Bones, Metabolic bone disease, Frameshift mutation, Young Adult, Internal medicine, Exome Sequencing, medicine, Humans, Gene Silencing, Bone pain, Biochemistry (medical), Paget’s disease of bone, Osteitis Deformans, medicine.disease, Radiography, Paget's disease of bone, Cancer research

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b922ab1142534eca3ee6bdfa912cc9Test
http://hdl.handle.net/11588/806085Test