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Human NME1 Protein expressed in Wheat germ - ABIN1312683
Yang, Chevolot, Géhin, Solassol, Mange, Souteyrand, Laurenceau: Improvement of protein immobilization for the elaboration of tumor-associated antigen microarrays: application to the sensitive and specific detection of tumor markers from breast cancer sera. dans Biosensors & bioelectronics 2012
NME1 promotes non-homologous end joining of DNA double-strand breaks
Deletion of these VP4 regions also inhibited the suppressive effect of VP4 on NME1-enhanced p53 signaling.
the potential roles that PARK7 and NDKA play in the management of acute stroke disease
The A allele in rs2159359 SNP in NME1 and the G allele in rs13222385 in EGFR were associated with worse overall survival in endometrial cancer. Both exhibited genome wide significance; rs13222385 remained significant after adjusting for prognostic clinical variables.
Study found that Nm23-H1 could be recruited to the 5'UTR of Sp1 mRNA. Its low expression levels along with that of SP1 are correlated with poor prognosis in patients with lung cancer. Also, lung cancer patients with higher levels of Sp1 and Nm23-H1 also exhibited high levels of hnRNPA2/B1, suggesting a positive correlation between the levels of Sp1, Nm23-H1 and hnRNPA2B1 during lung cancer formation.
ALDOC, CXCL11, LRP1b, and XAGE1 regulated by NME1, but not by NME1 variants lacking metastasis suppressor activity
Nm23-H1 participates in multiple steps of double-strand break repair (DSBR).
interacts with CFTR through reciprocal AMPK binding/control [review]
These results suggest a common molecular mechanism between myeloid differentiation of leukemia cells and migration of breast cancer cells depending on NM23 and EDG2 expression levels.
Studies indicate roles of nucleoside diphosphate kinase A NDPK-A (nm23-H1) S120G mutation in the prognosis of neuroblastoma and as a metastasis promoter [Review].
Nm23-H1 nucleoside diphosphate kinase (Nm23-H1) modulates the activities of chromatin modifiers through interaction with Epstein-Barr virus-encoded oncogenic antigens [Review].
NME1 enhanced ALDOC transcription, evidenced by increased expression of ALDOC pre-mRNA and activity of an ALDOC promoter-luciferase module. This is the first study to indicate that NME1 induces transcription through its direct binding to the promoter region of a target gene.
NME1 rs16949649 associated with increased susceptibility to gynecological cancer and rs2302254 was linked to reduced gastric cancer risk (Meta-Analysis)
Immunohistochemical expression of nm23H1 is not an effective tool to distinguish among the cases of BPH, adenocarcinoma of prostate with and without metastasis. Hence nm23H1 gene does not behave like an antimetastatic gene in prostatic lesions.
The positive expression rates of KAI1 and nm23 were significantly lower in laryngeal squamous cell carcinoma than normal laryngeal mucosa.
coexistence of high MACC1 and low NM23-H1 expression and tumor budding was associated with short overall survival
elevated NDKA was associated with severe characteristics of adenomas (>/=3 lesions, size >/= 1 cm or villous component). Setting specificity to 85%, NDKA showed a sensitivity of 30.19% and 29.82% for advanced adenomas and advanced neoplasia, respectively.
This study suggested that EGFR was an important predictive factor for the prognosis of the post-operative patients with colorectal carcinoma TNM stage I-II, and nm23 is important for predicting the prognosis of the patients with stage III-IV; it is better that EGFR and nm23 are as predictor of combination.
Results demonstrate that nm23 plays a vital role in decidualization in mice and humans and that nm23 gene expression is hormonally regulated.
NM23 might be an indicator of good prognosis in patients with breast cancer, although further researches need to be performed to confirm the prognostic value of NM23. [Meta-analysis; review]
Data identify NME1 as one of the two NME isoforms involved in class switch recombination (CSR) in B cells. Its knockdown leads to increased CSR. On the contrary of NME2, NME1 binds to S regions prior to stimulation.
Deletion of NME1 reduced total NDPK activity and exacerbated activation of the stress-related MAPK, JNK, in the liver in response to paraquat. NDPK activity protects cells from acute oxidative stress by inhibiting activation of JNK in mammal models.
EMMPRIN ensures proper actomyosin-driven maturation of competent endothelial junctions by forming a molecular complex with gamma-catenin (also known as junction plakoglobin) and Nm23 (also known as NME1), a nucleoside diphosphate kinase
data suggested that NME1 acts as a switcher or reprogramming factor which involves in oligodentrocyte versus neuron cell fate specification in vitro
NM23 deficiency promotes metastasis in a UV radiation-induced mouse model of human melanoma.
NME1 controls annexin IV and EF-1Balpha amounts by post-translational mechanisms.
data show a critical role for NM23 isoforms in limiting mutagenesis and suppressing UVR-induced melanomagenesis
GAPDH and NDPK are genetic modifiers of murine DDC-induced liver injury
The work provides a rare instance of nm23-1/NDPKA physiological functions in the mammary glands and reveals its implication as a modulator factor of proliferation and apoptosis in this tissue.
Ha-ras oncogene regulates morphogenesis, tumorigenesis, and metastasis through suppressing nm23 expression and modulation of immune cell function
Data suggested that nm23-M1/NDPK A was involved in the process of blastocyst implantation.
Data show that LMPAB reduced MMP-9 but enhanced nm23-H1 mRNA and protein expression.
suppressor of tumorigenicity 7 (ST7) and nonmetastatic 23 (NM23) are direct targets of PRMT5-containing BRG1 and hBRM complexes
NDPKB-dependent nm23-M1 gene (NDPKA) transactivation requires elements different from those involved in c-myc transactivation. cell death induced by c-myc overexpression or H(2)O(2) exposure was decreased in nm23-transfected compared to control BAF3 cells
The lack of NM23-M1 expression promotes metastasis in the SV40 animal model of liver carcinogenesis.
The data provide novel insight into the subunit composition of the epithelial CFTR/AMPK/NDPK complex, such that: CFTR interacts specifically with AMPK alpha1, gamma2 and NDPK-A and not NDPK-B or AMPK gamma1.
direct interaction between NM23-H1 and macrophage migration inhibitory factor (MIF) is critical for alleviation of MIF-mediated suppression of p53 activity
TfR1 is a downstream target of NDPKs and that reduced iron in Nme1(-/-)/Nme2(-/-) erythroblasts is inhibiting their development
Data show that embryonic fibroblasts from wild-type and NDPK A/B knockout mice demonstrate a similar reduction of G protein in mammalian cells.
NDPK A and NDPK B attenuated mRNA and protein levels of COX-2 by affecting TGF-beta-Smad2/3/4 signaling at the receptor level.
NDPKB is required for VEGF-induced angiogenesis and contributes to the correct localization of VEGF receptor type 2 and VE-cadherin at the endothelial adherens junctions.
Data show that NDPK B knockdown embryo results in a severe decrease in cardiac contractility.
NDPK-A exists in a functional cellular complex with AMPK and CFTR in airway epithelia, and NDPK-A catalytic function is required for the AMPK-dependent regulation of CFTR
The physical interaction between phytochrome A in the Pfr form and NDPK-In results in a significant increase in the kinase activity of NDPK-In. The results presented in this work indicate that NDPK-In may function as a protein kinase regulated by light.
This gene (NME1) was identified because of its reduced mRNA transcript levels in highly metastatic cells. Nucleoside diphosphate kinase (NDK) exists as a hexamer composed of 'A' (encoded by this gene) and 'B' (encoded by NME2) isoforms. Mutations in this gene have been identified in aggressive neuroblastomas. Two transcript variants encoding different isoforms have been found for this gene. Co-transcription of this gene and the neighboring downstream gene (NME2) generates naturally-occurring transcripts (NME1-NME2), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product.
NDP kinase A
, granzyme A-activated DNase
, metastasis inhibition factor nm23
, non-metastatic cells 1, protein (NM23A) expressed in
, nucleoside diphosphate kinase A
, tumor metastatic process-associated protein
, NDK A
, expressed in non-metastatic cells 1 protein
, expressed in non-metastatic cells 1, protein
, metastasis inhibition factor NM23
, nucleoside-diphosphate kinase 1
, nucleotide diphosphate kinase
, NDP kinase beta
, expressed in non-metastatic cells 1 protein (NM23A) (nucleoside diphosphate kinase)
, expressed in non-metastatic cells 1, protein (NM23A) (nucleoside diphosphate kinase)
, nucloside diphosphate kinase
, non-metastatic cells 2, protein (NM23B) expressed in
, non-metastatic cells 2b.1, protein (NM23B) expressed in
, nucleoside diphosphate kinase-Z1
, NME1-NME2 readthrough transcript
, expressed in non-metastatic cells 1
, NDK A2
, NDP kinase A2
, NM23/nucleoside diphosphate kinase A2
, ndk a1
, nucleoside diphosphate kinase A2
, NDK A 1
, NDK A 2
, NDK NBR-A
, NDK NBR-B
, NDP kinase A 1
, NDP kinase A 2
, nucleoside diphosphate kinase A 1
, nucleoside diphosphate kinase A 2
, nucleoside diphosphate kinase NBR-A
, nucleoside diphosphate kinase NBR-B
, nucleoside-diphosphate kinase NBR-A
, nucleoside-diphosphate kinase NBR-B
, NDK A1
, NDP kinase A1
, NM23/nucleoside diphosphate kinase A1
, ndk a2
, nucleoside diphosphate kinase A1
, NDP kinase I
, nucleoside diphosphate kinase 1
, nucleoside diphosphate kinase I
, NDK I
, NDPK I
, Nucleoside diphosphate kinase I