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抗Human RRM2 抗体:
抗Mouse (Murine) RRM2 抗体:
抗Rat (Rattus) RRM2 抗体:
Human Monoclonal RRM2 Primary Antibody for IF, IHC (p) - ABIN562744
Tang, Deng, Wang, Dai, Wang, Jiang, Li, Li, Sheng, Wu, Li, Zeng et al.: Quantitative phosphoproteome profiling of Wnt3a-mediated signaling network: indicating the involvement of ribonucleoside-diphosphate reductase M2 subunit phosphorylation at residue serine 20 in ... in Molecular & cellular proteomics : MCP 2007
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Human Monoclonal RRM2 Primary Antibody for IF, IHC (p) - ABIN2476387
Neinstein: Abdominal and flank pain as presenting symptoms of schwannoma. in Journal of adolescent health care : official publication of the Society for Adolescent Medicine 1989
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Cow (Bovine) Polyclonal RRM2 Primary Antibody for WB - ABIN2782440
Souglakos, Boukovinas, Taron, Mendez, Mavroudis, Tripaki, Hatzidaki, Koutsopoulos, Stathopoulos, Georgoulias, Rosell: Ribonucleotide reductase subunits M1 and M2 mRNA expression levels and clinical outcome of lung adenocarcinoma patients treated with docetaxel/gemcitabine. in British journal of cancer 2008
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Human Polyclonal RRM2 Primary Antibody for IF, WB - ABIN2452118
Takada, Shibata, Hiraoka, Masuda: Identification of ribonucleotide reductase protein R1 as an activator of microtubule nucleation in Xenopus egg mitotic extracts. in Molecular biology of the cell 2000
TP53 (显示 TP53 抗体) mutant cancer cells had elevation of ribonucleotide reductase subunit 1 (RRM1 (显示 RRM1 抗体)) and 2 (RRM2), which was reduced by inhibition of mTORC1.
Results indicate CREB1 (显示 CREB1 抗体) as a critical transcription factor of RRM2 which promotes tumor aggressiveness, and imply a significant correlation between CREB1 (显示 CREB1 抗体) and RRM2 in CRC (显示 CALR 抗体) specimens.
These findings suggest that the identified APLP2 (显示 APLP2 抗体), RRM2, and PRC1 (显示 PRC1 抗体) signature could be useful for distinguishing between benign (follicular adenoma) and malignant (follicular carcionma and follicular variant of papillary carcinoma) tumors of the thyroid follicular epithelium.
Data show that inhibition of sphingosine kinase-2 (显示 SPHK2 抗体) by ABC294640 is synergistically cytotoxic with gemcitabine toward three pancreatic cancer cell lines, resulting in decreased expression of both ribonucleotide reductase regulatory subunit M2 (RRM2) and c-MYC (显示 MYC 抗体) protein (Myc (显示 MYC 抗体)) in all three cell lines.
Based on the results of clinical trials, we conclude that Ribonucleotide reductase (RR) enzymes (RR1 (显示 RRM1 抗体) and RR2)inhibitors are viable treatment options, either as a monotherapy or as a combination in cancer chemotherapy. With the recent advances made in cancer biology, further development of RR inhibitors with improved efficacy and reduced toxicity is possible for treatment of variety of cancers.
Here we designed UC-rich and CU-rich 10-nt sequences for engagement of both RRM2 and RRM3 and demonstrated that the TIA-1 (显示 TIA1 抗体) RRM23 construct preferentially binds the UC-rich RNA ligand. Together our data support a specific mode of TIA-1 (显示 TIA1 抗体) RRM23 interaction with target oligonucleotides consistent with the role of TIA-1 (显示 TIA1 抗体) in binding RNA to regulate gene expression
These data suggest that VASH2 (显示 VASH2 抗体) reduces the chemosensitivity to gemcitabine in pancreatic cancer cells via JUN (显示 JUN 抗体)-dependent transactivation of RRM2.
HPV31 regulates RRM2 levels through expression of E7 and activation of the ATR (显示 ANTXR1 抗体)-Chk1 (显示 CHEK1 抗体)-E2F1 (显示 E2F1 抗体) DNA damage response, which is essential to combat replication stress upon entry into S-phase.
To the best of our knowledge, this is the first study that investigated the relationship of RRM1 (显示 RRM1 抗体) and RRM2 gene polymorphisms and Coronary artery disease (CAD (显示 CAD 抗体)).
The SCYL1- BP1 (显示 GORAB 抗体) affects the cell cycle through increasing steady state levels of Cyclin F (显示 CCNF 抗体) and RRM2 proteins, thus constituting a dual regulatory circuit.
This work reveals that binding of RRM1 (显示 RRM1 抗体) to RRM2 is essential for mammalian cells and provides the first loss-of-function model of the ribonucleotide reductase complex for genetic studies.
mice carrying extra alleles of the RNR (显示 REN1 抗体) regulatory subunit RRM2 (Rrm2(TG)) present supraphysiological RNR (显示 REN1 抗体) activity and reduced chromosomal breakage at fragile sites
analysis of transgenic overexpression of ribonucleotide reductase Rrm1 (显示 RRM1 抗体) and Rrm2 improves cardiac performance
Cinobufotalin significantly inhibits the growth of the xenografts of endometrial carcinoma Ishikawa in nude mice by inhibiting RRM2 expression.
Data suggest that RRM2 may be an important effector of progesterone signaling to induce cell proliferation and decidualization in uterus.
illegitimate recombination initiated by c-Myc (显示 MYC 抗体)
Adrenergic stimulation of brown adipocytes elevates ribonucleotide reductase subunit R2 in the proliferative stage of adipocyte development; mediating pathways include cAMP/PKA cascades, Src (显示 SRC 抗体) and Erk (显示 EPHB2 抗体) Map Kinases.
S Phase-specific transcription of the mouse ribonucleotide reductase R2 gene requires both a proximal repressive E2F (显示 E2F1 抗体)-binding site and an upstream promoter activating region
Chk1 is required for DNA replication at least through regulating RNR2 gene transcription.
results indicate that the affinity of the RNR (显示 REN1 抗体) R2 proteins for binding metals is determined by the nature of one specific residue in the vicinity of the dimetal site, namely the one that carries the tyrosyl radical in class Ia and Ib R2 proteins
This gene encodes one of two non-identical subunits for ribonucleotide reductase. This reductase catalyzes the formation of deoxyribonucleotides from ribonucleotides. Synthesis of the encoded protein (M2) is regulated in a cell-cycle dependent fashion. Transcription from this gene can initiate from alternative promoters, which results in two isoforms that differ in the lengths of their N-termini. Related pseudogenes have been identified on chromosomes 1 and X.
ribonucleoside-diphosphate reductase subunit M2
, ribonucleotide reductase M2 polypeptide
, ribonucleotide reductase small chain
, ribonucleotide reductase small subunit
, ribonucleoside-diphosphate reductase M2 chain
, Ribonucleotide reductase 2
, reductase M2 polypeptide variant 1
, reductase M2 polypeptide variant 2
, reductase M2 polypeptide variant 3a
, reductase M2 polypeptide variant 3b
, reductase M2 polypeptide variant 3c
, reductase M2 polypeptide variant 3d
, ribonucleotide reductase protein r2 class I