Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renata Kowara"'
Autor:
Tadeusz Pawełczyk, Tomasz Jastrzebski, Andrzej Kopacz, Grzegorz Gryglewski, Jacek Zieliński, Cezary Warezak, Robert Rzepko, Renata Kowara, Wiesław Kruszewski
Publikováno v:
Folia Histochemica et Cytobiologica, Vol 42, Iss 3, Pp 173-179 (2004)
The routine multidisciplinary management of colon cancer is based mainly on tumor staging, histology, grading and vascular invasion. In this approach, important individual information derived from molecular characteristics of the tumor may be missed,
Externí odkaz:
https://doaj.org/article/2d057031a81541bdaa1d9ebd2528bf0f
Publikováno v:
Neuroscience Letters. 430:197-202
Dihydropyrimidinase-like 3 (DPYSL3) is believed to play a role in neuronal differentiation, axonal outgrowth and neuronal regeneration, as well as cytoskeleton organization. Recently we have shown that glutamate excitotoxicity and oxidative stress re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e12a585a0a30be017e2994640bc5773e
https://doi.org/10.1016/j.neulet.2007.10.036
https://doi.org/10.1016/j.neulet.2007.10.036
Publikováno v:
Biochemical and Biophysical Research Communications. 363:190-193
Dihydropyrimidinase-like 3 (DPYSL3) and GAP43 are both involved in neurite outgrowth, a crucial process for the differentiation of neurons. The present study shows for the first time that DPYSL3 co-localizes with GAP43 in primary cortical neurons. Fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1d4bd2cc8d071f5c3baca8ebd4714d3
https://doi.org/10.1016/j.bbrc.2007.08.163
https://doi.org/10.1016/j.bbrc.2007.08.163
Publikováno v:
Brain Research. 1119:40-49
Dihydropyrimidinase-like 3 (DPYSL3), a member of TUC (TOAD-64/Ulip/CRMP), is believed to play a role in neuronal differentiation, axonal outgrowth and possibly in neuronal regeneration. Recently, we have shown that in primary cortical neurons (PCN) N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9466ce98b23805513b72d740a87ca378
https://doi.org/10.1016/j.brainres.2006.08.047
https://doi.org/10.1016/j.brainres.2006.08.047
Autor:
Kazimierz S. Kasprzak, Robert Y.S. Cheng, Renata Kowara, Aldona Karaczyn, Konstantin Salnikow
Publikováno v:
Toxicology and Applied Pharmacology. 205:1-10
B200 cells are Ni(II)-transformed mouse BALB/c-3T3 fibroblasts displaying a malignant phenotype and increased resistance to Ni(II) toxicity. In an attempt to find genes whose expression has been altered by the transformation, the Atlas Mouse Stress/T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::114b7703acb9517eab5ff34e2ce4875b
https://doi.org/10.1016/j.taap.2004.10.006
https://doi.org/10.1016/j.taap.2004.10.006
Autor:
Renata, Kowara, Filip, Gołebiowski, Paweł, Chrzan, Jaroslaw, Skokowski, Andrzej, Karmolinski, Tadeusz, Pawełczyk
Publikováno v:
Scopus-Elsevier
Searching for ways to improve the characterization of breast cancer we examined the relationship between the status of the FHIT gene transcript and amplification of c-myc and the c-erbB2 oncogene. Abnormal FHIT transcript was detected in 32 of 79 can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80a25bf09f908e583bb50a815fcdcd27
https://doi.org/10.18388/abp.2002_3792
https://doi.org/10.18388/abp.2002_3792
Publikováno v:
Chemical Research in Toxicology. 15:319-325
FHIT (Fragile Histidine Triad) is a human tumor suppressor gene. The Fhit protein is believed to inhibit tumor growth by inducing apoptosis through interaction with diadenosine triphosphate (Ap(3)A). The latter is first sequestered and eventually hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84594ce666270a9b8af1d75acfde923f
https://doi.org/10.1021/tx010112j
https://doi.org/10.1021/tx010112j
Publikováno v:
Molecular and Cellular Biochemistry. 226:49-55
The FHIT (fragile histidine triad) gene located at chromosome 3p14.2 has been proposed as a candidate tumor suppressor gene in human cancers. Fhit protein with the diadenosine 5',5'”-P1,P3-triphosphate (Ap3A) hydrolase activity is the protein produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b26f8bd489263962cdcc4c124936d911
https://doi.org/10.1023/a:1012729601270
https://doi.org/10.1023/a:1012729601270
Publikováno v:
Protein Expression and Purification. 18:320-326
The fragile histidine triad (Fhit) protein is a homodimeric protein with diadenosine 5',5"'-P(1),P(3)-triphosphate (Ap(3)A) asymmetrical hydrolase activity. We have cloned the human cDNA Fhit in the pPROEX-1 vector and expressed with high yield in Es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::942c65750a5d4ad60a8f91100ffba751
https://doi.org/10.1006/prep.1999.1199
https://doi.org/10.1006/prep.1999.1199
Publikováno v:
Molecular and Cellular Biochemistry. 209:69-77
Protein kinase C-γ (PKC-γ) contains two cysteine-rich regions (Cys1, Cys2) responsible for interaction with phospholipids. However, previous experiments suggested that, only Cys1 represents the high affinity site involved in diacylglycerol-dependen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0fff91a878720f02dcfb7c42f66c14b
https://doi.org/10.1023/a:1007063331593
https://doi.org/10.1023/a:1007063331593