Zobrazeno 1 - 10
of 108
pro vyhledávání: '"P. G. Rothberg"'
Publikováno v:
Case Reports in Hematology, Vol 2021 (2021)
Acute eosinophilic leukemia (AEL) is a rare form of acute myeloid leukemia (AML) that requires prompt exclusion of reactive etiologies of eosinophilia and identification of an underlying acute myeloid neoplasm. Myeloid neoplasms with prominent eosino
Externí odkaz:
https://doaj.org/article/d93bfee01b3f4e35913535be554e6d9b
Autor:
Jodi Ram, Gabrielle Flamm, Marlene Balys, Umayal Sivagnanalingam, Paul G. Rothberg, Anwar Iqbal, Jason R. Myers, Anthony Corbett, John M. Ashton, Jason H. Mendler
Publikováno v:
Blood Advances, Vol 1, Iss 8, Pp 500-503 (2017)
Externí odkaz:
https://doaj.org/article/acd9d1997f8b4dc1bf30dbd88d44488f
Autor:
Chi-Lun Chang, Ting-Sung Hsieh, T. Tony Yang, Karen G. Rothberg, D. Berfin Azizoglu, Elzibeth Volk, Jung-Chi Liao, Jen Liou
Publikováno v:
Cell Reports, Vol 5, Iss 3, Pp 813-825 (2013)
Endoplasmic reticulum (ER)-plasma membrane (PM) junctions are highly conserved subcellular structures. Despite their importance in Ca2+ signaling and lipid trafficking, the molecular mechanisms underlying the regulation and functions of ER-PM junctio
Externí odkaz:
https://doaj.org/article/af9cb6ddd2564e449a564842957003c3
Publikováno v:
Blood. 83:641-644
Rearrangements of chromosome band 11q23 are common in infant leukemias, comprising more than 70% of the observed chromosome abnormalities in children less than 1 year of age. The MLL gene, which is located at the 11q23 breakpoint in infant, childhood
Publikováno v:
Human genetics. 116(6)
Publikováno v:
Human genetics. 106(6)
Publikováno v:
Human genetics. 106(6)
Publikováno v:
Molecular and cellular biochemistry. 201(1-2)
Rotenone decreases the incidence of hepatocellular carcinoma and lowers rates of hepatocellular proliferation. In an effort to delineate mechanisms involved, the in vivo effect of rotenone on liver mitochondrial metabolism, apoptotic machinery as wel
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene
Publikováno v:
American journal of medical genetics. 87(2)
We have identified a family segregating von Hippel-Lindau (VHL) disease with a previously unreported T547A mutation in exon 1 of the VHL gene that causes a Tyr112 to Asn missense alteration in the protein. The mutation was identified by nucleotide se
Autor:
P G, Rothberg, S, Ponnuru, D, Baker, J F, Bradley, A I, Freeman, G W, Cibis, D J, Harris, D P, Heruth
Publikováno v:
Molecular carcinogenesis. 19(2)
The retinoblastoma gene (RB) encodes a tumor suppressor that is inactivated in a number of different types of cancer. We searched for gross alterations of this gene in tumors of the central nervous system by using Southern blot hybridization. A commo