Zobrazeno 1 - 10
of 1 336
pro vyhledávání: '"E, Kutz"'
Autor:
Choi, Keewhan
Publikováno v:
Biometrics, 1964 Sep 01. 20(3), 653-654.
Externí odkaz:
https://www.jstor.org/stable/2528506
Publikováno v:
Business First - Louisville; 5/23/94, Vol. 10 Issue 43, Who's Who in Health Care p10-B, 2p, 1 Black and White Photograph
Autor:
Shweta Singh, Wendy E. Kutz, Lauren W. Wang, Dieter P. Reinhardt, Michael W. Jenkins, Timothy J. Mead, Lauren C. Beene, Suneel S. Apte
Publikováno v:
Matrix Biol
Mutations in the secreted metalloproteinase ADAMTS10 cause recessive Weill-Marchesani syndrome (WMS), comprising ectopia lentis, short stature, brachydactyly, thick skin and cardiac valve anomalies. Dominant WMS caused by FBN1 mutations is clinically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04bd6465971d92453483f0464f5e4ab5
https://pubmed.ncbi.nlm.nih.gov/30201140
https://pubmed.ncbi.nlm.nih.gov/30201140
Publikováno v:
Journal of Cell Communication and Signaling
Loss-of-function mutations in the gene WISP3 cause the autosomal recessive human skeletal disease Progressive Pseudorheumatoid Dysplasia, whereas mice with knockout mutations of Wisp3 have no phenotype. The lack of a phenotype in the Wisp3 knockout m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a95b0255f6b1413cd477a53dec0e6d2
http://europepmc.org/articles/PMC2721080
http://europepmc.org/articles/PMC2721080
Autor:
Qiyuan, Pang1 (AUTHOR), Changyang, Lin2 (AUTHOR), Gaigai, Li2 (AUTHOR), Ju, Qiu2 (AUTHOR), Xun, Zhou2 (AUTHOR) 3453730998@qq.com
Publikováno v:
PLoS ONE. 12/30/2024, Vol. 19 Issue 12, p1-10. 10p.
Autor:
Zakynthinos, George E.1 (AUTHOR) gzakynthinos2@gmail.com, Tsolaki, Vasiliki2 (AUTHOR) vasotsolaki@yahoo.com, Xanthopoulos, Andrew3 (AUTHOR) andrewvxanth@gmail.com, Karavidas, Nikitas2 (AUTHOR) nikitaskaravidas@gmail.com, Vazgiourakis, Vasileios2 (AUTHOR) vasvazg@yahoo.com, Bardaka, Fotini2 (AUTHOR) bardakafotini@yahoo.gr, Giamouzis, Grigorios3 (AUTHOR) grgiamouzis@gmail.com, Pantazopoulos, Ioannis4 (AUTHOR) ipantazop@uth.gr, Makris, Demosthenes2 (AUTHOR) dimomakris@uth.gr
Publikováno v:
Journal of Clinical Medicine. Nov2024, Vol. 13 Issue 22, p6750. 14p.
Autor:
Haddad, Monoem1 (AUTHOR) mhaddad@qu.edu.qa
Publikováno v:
Symmetry (20738994). Nov2024, Vol. 16 Issue 11, p1485. 13p.
Autor:
Rahmani, Mehran1 (AUTHOR) mrahma61@asu.edu, Redkar, Sangram1 (AUTHOR)
Publikováno v:
Biomimetics (2313-7673). Nov2024, Vol. 9 Issue 11, p666. 13p.
Autor:
Joseph E. Kutz, Christina L. Kaufman, Yorell Manon-Matos, Antonio Rampazzo, Francis Papay, Bahar Bassiri Gharb, Linda Bright
Publikováno v:
Plastic and reconstructive surgery. 136(3)
Amputation of all fingers (metacarpal hand) can be functionally equivalent to hand amputation. Multidigit allotransplantation can benefit patients who require a full complement of fingers to return to their preinjury activities. The authors investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24878852f6bc2c561d47913b62e132aa
https://pubmed.ncbi.nlm.nih.gov/26313825
https://pubmed.ncbi.nlm.nih.gov/26313825
Publikováno v:
Current Drug Discovery Technologies. 3:189-197
Computer assisted, or in silico, drug discovery approaches play an important role in the search for small molecule hits and leads. These include structure- and ligand-based methods, as well as data mining and QSAR. They are used to analyze and predic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fbc5054576284ee4517857d765c141c
https://doi.org/10.2174/157016306780136790
https://doi.org/10.2174/157016306780136790