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[PDF] Top 20 Cyclin-dependent kinases in C. elegans

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Cyclin-dependent kinases in C. elegans

Cyclin-dependent kinases in C. elegans

... In higher eukaryotes, Cdk7 plays a unique dual role in reg- ulating the activity of other CDKs as well as transcription. Cdk7 forms the kinase subunit of CAK, the CDK activat- ing kinase responsible for the activating ... See full document

12

Recent advances of cyclin-dependent kinases as potential therapeutic targets in HR+/HER2− metastatic breast cancer: a focus on ribociclib

Recent advances of cyclin-dependent kinases as potential therapeutic targets in HR+/HER2− metastatic breast cancer: a focus on ribociclib

... of cyclin D-CDK4/6-Rb pathways involving the use of biomarkers as measures of response will likely be expected to undergo for optimal benefit of patients with various cancer ... See full document

13

Omega 3 polyunsaturated fatty acids inhibit cell proliferation by regulating cell cycle in fad3b transgenic mouse embryonic stem cells

Omega 3 polyunsaturated fatty acids inhibit cell proliferation by regulating cell cycle in fad3b transgenic mouse embryonic stem cells

... G1/S-specific cyclin-D1; Ccne1: G1/S-specific cyclin-E1; Cdk2: Cyclin- dependent kinase 2; Cdk4: Cyclin-dependent kinase 4; Cdk6: Cyclin-dependent kinase 6; Cdkn1a: ... See full document

9

<p>Efficacy and Safety of Cyclin-Dependent Kinases 4 and 6 Inhibitors in HR+/HER2− Advanced Breast Cancer</p>

<p>Efficacy and Safety of Cyclin-Dependent Kinases 4 and 6 Inhibitors in HR+/HER2&minus; Advanced Breast Cancer</p>

... of cyclin-dependent kinases 4 and 6 inhibitors (CDKi) combined with endocrine therapy (ET) in women with hormone receptor (HR)- positive, human epidermal growth factor receptor 2 (HER2)-negative ... See full document

10

Inhibition of CDK4/6 as a novel therapeutic option for neuroblastoma

Inhibition of CDK4/6 as a novel therapeutic option for neuroblastoma

... mTOR- dependent [10, 18], or by inhibitors of glycogen synthase kinase 3 β (GSK3 β ), which phosphorylates cyclin D1 at Thr-286 suggested to regulate the turnover and the intra- cellular distribution of ... See full document

8

Kaposi&#039;s Sarcoma-Associated Herpesvirus K-bZIP Protein Is Phosphorylated by Cyclin-Dependent Kinases

Kaposi's Sarcoma-Associated Herpesvirus K-bZIP Protein Is Phosphorylated by Cyclin-Dependent Kinases

... recognition motifs: SPER, TPMR, SPPR, and TPPR (which is also found in K-bZIP). Under these conditions, ORF 73 was not radioactively labeled (Fig. 6B), even though Western blot analysis of the kinase reaction ... See full document

10

The Oxidative Stress Response in Caenorhabditis elegans Requires the GATA Transcription Factor ELT-3 and SKN-1/Nrf2

The Oxidative Stress Response in Caenorhabditis elegans Requires the GATA Transcription Factor ELT-3 and SKN-1/Nrf2

... specific kinases can either promote or prevent translocation from the cytosol to the nucleus, where gene expression can then be ...2015). C. elegans lacks a Keap1 ortholog; however, the C. ... See full document

14

Antitumoral effects of cyclin-dependent kinases inhibitors CR8 and MR4 on chronic myeloid leukemia cell lines

Antitumoral effects of cyclin-dependent kinases inhibitors CR8 and MR4 on chronic myeloid leukemia cell lines

... by cyclin-dependent kinases (CDKs) which require association with cyclins and phosphoryl- ation to be catalytically active ...of kinases [16] and limited toxicity and side effects [17, 18] ... See full document

16

Differential requirements for STRAD in LKB1 dependent functions in C  elegans

Differential requirements for STRAD in LKB1 dependent functions in C elegans

... early C. elegans embryos, mutations in par-4 or par-1 similarly result in the loss of the asymmetric distribution of the early fate determinants, suggesting that they function in the same process (Guo and ... See full document

10

The effect of cyclic adenosine monophosphate (camp) modulators on the activity of selected antimalarial drugs

The effect of cyclic adenosine monophosphate (camp) modulators on the activity of selected antimalarial drugs

... the ste6 gene of saccharomyces cerevisiae with pfmdr1 gene of Plasmodium falciparum. and Geyer, J.A. Cyclin-dependent protein kinases as therapeutic drug targets for antimalarial drug de[r] ... See full document

123

S-Like-Phase Cyclin-Dependent Kinases Stabilize the Epstein-Barr Virus BDLF4 Protein To Temporally Control Late Gene Transcription

S-Like-Phase Cyclin-Dependent Kinases Stabilize the Epstein-Barr Virus BDLF4 Protein To Temporally Control Late Gene Transcription

... of cyclin-dependent ki- nase (CDK) inhibitors that downregulated the expression of L genes without any im- pact on viral DNA replication through destabilization of the BDLF4 ...that cyclin A- and ... See full document

16

Targeting Cyclin-Dependent Kinases in Synovial Sarcoma: Palbociclib as a Potential Treatment for Synovial Sarcoma Patients.

Targeting Cyclin-Dependent Kinases in Synovial Sarcoma: Palbociclib as a Potential Treatment for Synovial Sarcoma Patients.

... which may thus potentially translate into higher activity in the clinic. Numerous potential combination therapies can be investigated, including various chemotherapeutics, small molecule inhibitors, and targeted ... See full document

8

Targeting the cyclin dependent kinases (CDK) 4/6 in estrogen receptor positive breast cancers

Targeting the cyclin dependent kinases (CDK) 4/6 in estrogen receptor positive breast cancers

... (PD 0332991; Pfizer) is furthest along in clinical develop- ment, having received US Food and Drug Administration (FDA) approval on 3 February 2015 for the first-line treat- ment of advanced post-menopausal ER+, ... See full document

11

The PHOA and PHOB Cyclin-Dependent Kinases Perform an Essential Function in Aspergillus nidulans

The PHOA and PHOB Cyclin-Dependent Kinases Perform an Essential Function in Aspergillus nidulans

... Figure 4.—PHOA and PHOB play an essential function. (A) Ascospores of (a) a cross between a strain with deletion of phoA to a strain with deletion of phoB (⌬phoA:pyrG ; pyroA4 ⫻ ⌬phoB:pyroA; pyrG89), (b) self-cross of ... See full document

12

Rheb1 promotes tumor progression through mTORC1 in MLL-AF9-initiated murine acute myeloid leukemia

Rheb1 promotes tumor progression through mTORC1 in MLL-AF9-initiated murine acute myeloid leukemia

... cyclins, cyclin-dependent kinases (CDKs) [41], and CDK inhibitors (CKIs) [42], we also ex- amined the expression of these genes and observed that the mRNA expressions of p18, p21, p27, and p57 were ... See full document

14

Inhibitors of cyclin-dependent kinases as cancer therapeutics.

Inhibitors of cyclin-dependent kinases as cancer therapeutics.

... The findings in antitumor experiments described above were counter to the concern that basic processes such as transcription would make poor targets for therapeutics as they would not select for cancer cells and would ... See full document

88

Synthesis of ring constrained thiazolylpyrimidines: inhibitors of cyclin dependent kinases

Synthesis of ring constrained thiazolylpyrimidines: inhibitors of cyclin dependent kinases

... p53 is a small 53 kDa protein which has the authority to halt cell division and/or induce apoptosis when activated. In normal cells p53 is kept at low levels and in an inactive state through its association with the ... See full document

185

Investigation of the role of cyclin dependent kinases in neuronal apoptosis

Investigation of the role of cyclin dependent kinases in neuronal apoptosis

... The Cip/Kip family of CKIs is characterised by their binding to preformed Cdk/cyclin complexes (Harper et aL, 1993; Polyak et aL, 1994; Lee et aL, 1995) (Figure 1.2). In vitro, these CKIs can block the activity of ... See full document

204

Cyclin dependent kinases

Cyclin dependent kinases

... related kinases such as Cdk4 and Cdk6 mostly function by phosphorylating transcription regulators such as Rb or Smads [3,25], and the archetypal cell-cycle kinase Cdk1 also phosphorylates multiple transcription ... See full document

10

Inflammasome inhibitors: promising therapeutic approaches against cancer

Inflammasome inhibitors: promising therapeutic approaches against cancer

... and cyclin-dependent kinases [114], and activation of the p53 protein [114], leading to reductions in cancer cell proliferation, invasion, and ... See full document

13

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