المؤلفون: Castro, B., Candelaria, J.I., Austin, M.M., Shuster, C.B., Gifford, C.A., Denicol, A.C., Hernandez Gifford, J.A.

المساهمون: National Institute of General Medical Sciences, USDA NIFA

المصدر: Theriogenology ; volume 214, page 57-65 ; ISSN 0093-691X

الاتاحة: http://dx.doi.org/10.1016/j.theriogenology.2023.10.010
https://api.elsevier.com/content/article/PII:S0093691X23004041?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0093691X23004041?httpAccept=text/plain

المؤلفون: Forrest, K.K., Flores, V.V., Gurule, S.C., Soto-Navarro, S., Shuster, C.B., Gifford, C.A., Gifford, J.A. Hernandez

المصدر: Animal Reproduction Science ; volume 237, page 106927 ; ISSN 0378-4320

الاتاحة: http://dx.doi.org/10.1016/j.anireprosci.2022.106927
https://api.elsevier.com/content/article/PII:S0378432022000069?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0378432022000069?httpAccept=text/plain

المؤلفون: Chiang, Y.-C., Park, I.-Y., Terzo, E.A., Tripathi, D.N., Mason, F.M., Fahey, C.C., Karki, M., Shuster, C.B., Sohn, B.-H., Chowdhury, P., Powell, R.T., Ohi, R., Tsai, Y.S., De Cubas, A.A., Khan, A., Davis, I.J., Strahl, B.D., Parker, J.S., Dere, R., Walke, C.L., Rathmell, W.K.

المصدر: Cancer Research, 78(12)

مصطلحات موضوعية: renal cell carcinoma, human cell, gene function, cancer growth, gene loss, reverse transcription polymerase chain reaction, Western blotting, priority journal, incubation time, staining, cell viability, histone methylation, human, haploinsufficiency, gene, immunofluorescence, single nucleotide polymorphism, genomic instability, cell count, gene mutation, kidney proximal tubule, controlled study, allele, SETD2 gene, carcinogenesis, genetic variability

Relation: https://doi.org/10.17615/vwc2-xf64; https://cdr.lib.unc.edu/downloads/cc08hq41d?file=thumbnail; https://cdr.lib.unc.edu/downloads/cc08hq41d

الاتاحة: https://doi.org/10.17615/vwc2-xf64
https://cdr.lib.unc.edu/downloads/cc08hq41d?file=thumbnail
https://cdr.lib.unc.edu/downloads/cc08hq41d

المؤلفون: Magedov I.V., Frolova L., Manpadi M., Bhoga U.D., Tang H., Evdokimov N.M., George O., Hadje Georgiou K., Renner S., Getlik M., Kinnibrugh T.L., Fernandes M.A., Van Slambrouck S., Steelant W.F.A., Shuster C.B., Rogelj S., Van Otterlo W.A.L., Kornienko A.

مصطلحات موضوعية: 2 hydroxy 7 (3,4,5 trimethoxyphenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 4 (2 hydroxy 3 methoxyphenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (3 bromo 4,5 dimethoxyphenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (3 bromophenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (3,4,5 trimethoxyphenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (3,5 dibromo 2 hydroxyphenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (3,5 dibromophenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (3,5 dibromophenyl) 3 methyl 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (4 bromo 2 thienyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (5 bromo 2 hydroxy 3 methoxyphenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (5 bromo 2 hydroxy 3 methoxyphenyl) 3 methyl 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (5 bromo 2 hydroxyphenyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (5 bromo 2 hydroxyphenyl) 3 methyl 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (5 bromo 3 pyridinyl) 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 4 (5 bromo 3 pyridinyl) 3 methyl 1,4,7,8 tetrahydro 5h furo[3,4 b]pyrazolo[4,3 e]pyridin 5 one, 7 (3 bromo 4,5 dimethoxyphenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 7 (3,4,5 trimethoxyphenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 7 (3,5 dibromo 2 hydroxyphenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 7 (3,5 dibromophenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 7 (4 bromo 2 thienyl) 7,11 dihydrobenzo[h]furo[3,4 b] quinolin 8(10h) one, 7 (5 bromo 2 hydroxy 3 methoxyphenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 7 (5 bromo 2 hydroxyphenyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, 7 (5 bromo 3 pyridinyl) 7,11 dihydrobenzo[h]furo[3,4 b]quinolin 8(10h) one, antineoplastic agent, beta tubulin, dihydropyridopyrazole derivative, heterocyclic compound, podophyllotoxin, tubulin, unclassified drug

Relation: Journal of Medicinal Chemistry; 54; 12; http://www.scopus.com/inward/record.url?eid=2-s2.0-79959480967&partnerID=40&md5=d9614c808abbad0880eaba5fd373337e; 222623; http://hdl.handle.net/10019.1/16683

الاتاحة: http://hdl.handle.net/10019.1/16683
http://www.scopus.com/inward/record.url?eid=2-s2.0-79959480967&partnerID=40&md5=d9614c808abbad0880eaba5fd373337e
https://doi.org/10.1021/jm200410r

المؤلفون: SHUSTER, C.B., HERMAN, I.M.

المصدر: Microcirculation ; volume 5, issue 4, page 239-257 ; ISSN 1073-9688 1549-8719

الاتاحة: http://dx.doi.org/10.1111/j.1549-8719.1998.tb00073.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1549-8719.1998.tb00073.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1549-8719.1998.tb00073.x

المؤلفون: Shuster, C.B., Burgess, D.R.

المصدر: Proceedings of the National Academy of Sciences of the United States of America. 3/19/2002, Vol. 99 Issue 6, p3633. 12p. 33 Diagrams.

مصطلحات موضوعية: *CYTOKINESIS, *CHROMOSOMES, *CELL division

المؤلفون: Allen, P.G., Shuster, C.B.

المصدر: Biochemistry. 11/12/96, Vol. 35 Issue 45, p14062. 8p. 2 Diagrams, 2 Charts, 6 Graphs.

مصطلحات موضوعية: *PHALLOIDINE, *ACTIN, *PROTEIN binding