المؤلفون: Ma, Van K, Mao, Rong, Toth, Jessica N, Fulmer, Makenzie L, Egense, Alena S, Shankar, Suma P

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Clinical Research, Brain Disorders, Rare Diseases, Congenital Structural Anomalies, Intellectual and Developmental Disabilities (IDD), Pediatric, Congenital, Quality Education, chromosome 15, developmental delay, hyperphagia, imprinting disorders, obesity, uniparental disomy, Clinical Sciences, Oncology and Carcinogenesis, Clinical sciences, Oncology and carcinogenesis

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0kn6584n

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, Ron H.N., Whirl-Carrillo, Michelle, Weck, Karen E.

المصدر: Pratt , V M , Cavallari , L H , Fulmer , M L , Gaedigk , A , Hachad , H , Ji , Y , Kalman , L V , Ly , R C , Moyer , A M , Scott , S A , van Schaik , R H N , Whirl-Carrillo , M & Weck , K E 2023 , ' CYP3A4 and CYP3A5 Genotyping Recommendations : A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, ....

الاتاحة: https://pure.eur.nl/en/publications/e44bd105-480e-4bd7-86aa-c15e336d6981
https://doi.org/10.1016/j.jmoldx.2023.06.008
http://www.scopus.com/inward/record.url?scp=85168427735&partnerID=8YFLogxK

المؤلفون: Fulmer, Makenzie L., Si, Yue, Best, D. Hunter

المصدر: Diagnostic Molecular Pathology ; page 255-266 ; ISBN 9780128228241

الاتاحة: http://dx.doi.org/10.1016/b978-0-12-822824-1.00024-9
https://api.elsevier.com/content/article/PII:B9780128228241000249?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:B9780128228241000249?httpAccept=text/plain

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, R. H.N., Whirl-Carrillo, Michelle, Weck, Karen E.

المصدر: Pratt , V M , Cavallari , L H , Fulmer , M L , Gaedigk , A , Hachad , H , Ji , Y , Kalman , L V , Ly , R C , Moyer , A M , Scott , S A , van Schaik , R H N , Whirl-Carrillo , M & Weck , K E 2022 , ' TPMT and NUDT15 Genotyping Recommendations : A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, ....

الاتاحة: https://pure.eur.nl/en/publications/0c57d93a-8856-4864-afdf-283c0a8c7453
https://doi.org/10.1016/j.jmoldx.2022.06.007
http://www.scopus.com/inward/record.url?scp=85139374647&partnerID=8YFLogxK

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., Turner, Amy J., van Schaik, Ron H.N., Whirl-Carrillo, Michelle, Weck, Karen E.

المصدر: The Journal of Molecular Diagnostics; October 2024, Vol. 26 Issue: 10 p851-863, 13p

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., Turner, Amy J., van Schaik, Ron H.N., Whirl-Carrillo, Michelle, Weck, Karen E.

المصدر: The Journal of Molecular Diagnostics ; volume 26, issue 10, page 851-863 ; ISSN 1525-1578

الاتاحة: https://doi.org/10.1016/j.jmoldx.2024.05.015
https://api.elsevier.com/content/article/PII:S1525157824001545?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1525157824001545?httpAccept=text/plain

المؤلفون: Ma,Van K, Mao,Rong, Toth,Jessica N, Fulmer,Makenzie L, Egense,Alena S, Shankar,Suma P

مصطلحات الفهرس: The Application of Clinical Genetics, Review, info:eu-repo/semantics/article

URL: https://www.dovepress.com/prader-willi-and-angelman-syndromes-mechanisms-and-management-peer-reviewed-fulltext-article-TACG
info:eu-repo/semantics/altIdentifier/doi/10.2147/TACG.S372708

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, Ron H. N., Whirl-Carrillo, Michelle, Weck, Karen E.

المساهمون: Medical and Molecular Genetics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Cytochrome P-450 CYP3A, Molecular pathology, Pharmacists, Pharmacogenetics, Genotype

وصف الملف: application/pdf

Relation: The Journal of Molecular Diagnostics; https://hdl.handle.net/1805/44401

الاتاحة: https://hdl.handle.net/1805/44401

المؤلفون: Lewis, Robert G., O’Shea, John, Best, D. Hunter, Fulmer, Makenzie L.

المصدر: Advances in Molecular Pathology ; volume 6, issue 1, page 175-186 ; ISSN 2589-4080

الاتاحة: http://dx.doi.org/10.1016/j.yamp.2023.08.006
https://api.elsevier.com/content/article/PII:S258940802300025X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S258940802300025X?httpAccept=text/plain

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, R. H. N., Whirl-Carrillo, Michelle, Weck, Karen E.

المساهمون: Medical and Molecular Genetics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: PGx Working Group, minimum panel of variant alleles, extended panel of variant alleles, TPMT and NUDT15 PGx testing, thiopurine S-methyltransferase (TPMT), nudix hydrolase 15 (NUDT15)

وصف الملف: application/pdf

Relation: Journal of Molecular Diagnostics; Pratt, V. M., Cavallari, L. H., Fulmer, M. L., Gaedigk, A., Hachad, H., Ji, Y., Kalman, L. V., Ly, R. C., Moyer, A. M., Scott, S. A., van Schaik, R. H. N., Whirl-Carrillo, M., & Weck, K. E. (2022). TPMT and NUDT15 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase. The Journal of Molecular Diagnostics, 24(10), 1051–1063. https://doi.org/10.1016/j.jmoldx.2022.06.007; https://hdl.handle.net/1805/41274

الاتاحة: https://hdl.handle.net/1805/41274

المؤلفون: Fulmer, Makenzie L., Thewke, Douglas P.

المصدر: ETSU Faculty Works.

مصطلحات موضوعية: 2-AG, AEA, atherosclerosis, cannabinoids, CB1, CB2, ischemia/reperfusion., Biomedical Sciences

الاتاحة: https://dc.etsu.edu/etsu-works/10500

المؤلفون: Fulmer, Makenzie L., Englehaupt, Emilee, Garst, Chris, Brown, Stacy D.

المصدر: ETSU Faculty Works.

مصطلحات موضوعية: receptor deficiency, atherosclerotic lesion, Pharmaceutical Sciences, Chemicals and Drugs, Pharmacy and Pharmaceutical Sciences

الاتاحة: https://dc.etsu.edu/etsu-works/5271

المؤلفون: Margraf, Rebecca L., Alexander, Rachel Z., Fulmer, Makenzie L., Miller, Christine, Coupal, Elena, Mao, Rong

الاتاحة: http://dx.doi.org/10.22541/au.165053552.26865967/v1

المؤلفون: Fulmer, Makenzie L., Razzaqi, Faisal, Andersen, Erica, Toydemir, Reha, Hong, Bo

المصدر: Cancer Genetics ; volume 252-253, page S6-S7 ; ISSN 2210-7762

الاتاحة: http://dx.doi.org/10.1016/j.cancergen.2021.01.029
https://api.elsevier.com/content/article/PII:S2210776221000351?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2210776221000351?httpAccept=text/plain

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, R.H.N., Whirl-Carrillo, Michelle, Weck, Karen E.

المصدر: The Journal of Molecular Diagnostics; October 2022, Vol. 24 Issue: 10 p1051-1063, 13p

المؤلفون: Thewke, Douglas P., Kou, Jianqun, Fulmer, Makenzie L., Xie, Qian

المصدر: Current Human Cell Research and Applications ; Regulation of Signal Transduction in Human Cell Research ; page 155-181 ; ISSN 2522-073X 2522-0748 ; ISBN 9789811072956 9789811072963

الاتاحة: http://dx.doi.org/10.1007/978-981-10-7296-3_8
http://link.springer.com/content/pdf/10.1007/978-981-10-7296-3_8

المؤلفون: Fulmer, Makenzie L., Thewke, Douglas P.

المصدر: ETSU Faculty Works

مصطلحات موضوعية: 2-AG, AEA, atherosclerosis, cannabinoids, CB1, CB2, ischemia/reperfusion, Biomedical Sciences

Relation: https://dc.etsu.edu/etsu-works/10500; https://doi.org/10.2174/1871529X18666180206161457

الاتاحة: https://dc.etsu.edu/etsu-works/10500
https://doi.org/10.2174/1871529X18666180206161457

المؤلفون: Fulmer, Makenzie L., Englehaupt, Emilee, Garst, Chris, Brown, Stacy D.

المصدر: ETSU Faculty Works

مصطلحات موضوعية: receptor deficiency, atherosclerotic lesion, Pharmaceutical Sciences, Chemicals and Drugs, Pharmacy and Pharmaceutical Sciences

Relation: https://dc.etsu.edu/etsu-works/5271

الاتاحة: https://dc.etsu.edu/etsu-works/5271

المؤلفون: Fulmer, Makenzie L, Englehaupt, Emilee, Garst, Chris, Brown, Stacy, Thewke, Douglas

المصدر: Arteriosclerosis, Thrombosis, and Vascular Biology ; volume 36, issue suppl_1 ; ISSN 1079-5642 1524-4636

الاتاحة: http://dx.doi.org/10.1161/atvb.36.suppl_1.643

المؤلفون: Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, R.H.N., Whirl-Carrillo, Michelle, Weck, Karen E.

المصدر: The Journal of Molecular Diagnostics; 20230101, Issue: Preprints