Zobrazeno 1 - 10
of 4 576
pro vyhledávání: '"M, Kupfer"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Journal des voyages, découvertes et navigations modernes, 1829 Sep 01. 43(131), 347-348.
Externí odkaz:
https://www.jstor.org/stable/45118123
Publikováno v:
CAA Reviews.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dris___01178::a2b3b8289479f7ad4de54d9ae2ab8166
https://doi.org/10.3202/caa.reviews.2020.16
https://doi.org/10.3202/caa.reviews.2020.16
Autor:
Dupré, S.
Publikováno v:
CAA Reviews
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::c719b632f9c9709fabfdddfdd7279967
https://dare.uva.nl/personal/pure/en/publications/review-of-m-kupfer-2016-art-and-optics-in-the-hereford-map-an-english-mappa-mundi-c-1300(68035aed-6761-4f5c-a719-2cfd22898c4d).html
https://dare.uva.nl/personal/pure/en/publications/review-of-m-kupfer-2016-art-and-optics-in-the-hereford-map-an-english-mappa-mundi-c-1300(68035aed-6761-4f5c-a719-2cfd22898c4d).html
Autor:
Anne Olazabal-Herrero, Boxue He, Youngho Kwon, Abhishek K. Gupta, Arijit Dutta, Yuxin Huang, Prajwal Boddu, Zhuobin Liang, Fengshan Liang, Yaqun Teng, Li Lan, Xiaoyong Chen, Huadong Pei, Manoj M. Pillai, Patrick Sung, Gary M. Kupfer
Publikováno v:
Cell Reports, Vol 43, Iss 1, Pp 113610- (2024)
Summary: Fanconi anemia (FA) is characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. The central FA protein complex FANCI/FANCD2 (ID2) is activated by monoubiquitination and recruits DNA repair proteins for inter
Externí odkaz:
https://doaj.org/article/bc92b447e5014f469f04a528e03fd245
Autor:
Fengshan Liang, Adam S. Miller, Simonne Longerich, Caroline Tang, David Maranon, Elizabeth A. Williamson, Robert Hromas, Claudia Wiese, Gary M. Kupfer, Patrick Sung
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-8 (2019)
In the Fanconi anemia pathway, deubiquitination of FANCD2 is a fundamental regulatory step. Here, the authors have developed a set of biochemical tools to reconstitute FANCD2 deubiquitination by recombinant USP1-UAF1-RAD51AP1 and reveal critical mech
Externí odkaz:
https://doaj.org/article/c6be56908081470bb7bc5319e965b081
Autor:
Sharon Noy-Lotan, Orly Dgany, Nathaly Marcoux, Ayelet Atkins, Gary M. Kupfer, Linette Bosques, Christine Gottschalk, Orna Steinberg-Shemer, Benny Motro, Hannah Tamary
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Congenital dyserythropoietic anemia type I (CDA I) is an autosomal recessive disease characterized by moderate to severe macrocytic anemia and pathognomonic morphologic abnormalities of the erythroid precursors, including spongy heterochromatin. The
Externí odkaz:
https://doaj.org/article/de2db599c3204c6095f47339336c7633
Autor:
Neil Pathak, BS, Alana M. Munger, MD, Ahmad Charifa, MD, William B. Laskin, MD, Emily Bisson, APRN, CPNP, Gary M. Kupfer, MD, Lee E. Rubin, MD
Publikováno v:
Arthroplasty Today, Vol 6, Iss 1, Pp 52-58.e1 (2020)
Hemophilia A is a rare genetic disorder involving a deficiency of clotting factor VIII. Coagulation factor replacement therapy has prolonged the life expectancy of patients with hemophilia, but recurrent hemarthrosis of major joints is often a common
Externí odkaz:
https://doaj.org/article/c35494b2f541495d88c935d63d2eedad
Autor:
Hilary A. Uyhelji, Doris M. Kupfer, Vicky L. White, Melinda L. Jackson, Hans P. A. Van Dongen, Dennis M. Burian
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-17 (2018)
Abstract Background Although sleep deprivation is associated with neurobehavioral impairment that may underlie significant risks to performance and safety, there is no reliable biomarker test to detect dangerous levels of impairment from sleep loss i
Externí odkaz:
https://doaj.org/article/87b5094048414ecdb2f05b85c0dfd5c1
Autor:
Susree Modepalli, Sandra Martinez-Morilla, Srividhya Venkatesan, James Fasano, Katerina Paulsen, Dirk Görlich, Shilpa Hattangadi, Gary M. Kupfer
Publikováno v:
Experimental Hematology. 114:22-32
Erythroid nuclear condensation is a complex process in which compaction to one-tenth its original size occurs in an active nucleus simultaneously undergoing transcription and cell division. We previously found that the nuclear exportin Exportin7 (Xpo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c916cde852c0308654a635d15bcb3d
https://doi.org/10.1016/j.exphem.2022.08.001
https://doi.org/10.1016/j.exphem.2022.08.001