There are over 500 known
human kinases and 10s of thousands of possible proteins they can target.
No. 5,817,479, entitled
Human Kinase Homologs, claims 44 ESTs which are fragments of genes encoding protein kinases.
Not exact matches
Cunningham and her postdoc at the time, Christine Kirvan, found that the antibodies literally bind to
human neurons, activating an enzyme called calcium / calmodulin - dependent protein (CaM)
kinase II.
The researchers observed the effect of the synthetically produced molecule, JK - 31, on the growth and proliferation of a model
human breast cancer cell line and found that it effectively blocked the protein cyclin - dependent
kinase 1 (CDK1), which plays a key part in the process of the division of cancer cells, and therefore inhibited the proliferation of the cells.
The results showed that, when applied, a long - term inhibition of Rho -
kinase signaling increased the expressions of chondrocyte - specific genes and differentiation markers in
human chondrosarcoma 2/8 cells.
«There are more than 500
kinases in the
human body; and many of them are essential building - blocks of life,» Laufer explains.
The Structural Genomics Consortium at the University of North Carolina at Chapel Hill (SGC - UNC), in partnership with the DiscoverX Corporation, has reached the milestone halfway point in its development of the
Kinase Chemogenomic Set, a potent group of inhibitors which allow deeper exploration of the
human kinome, a family of enzymes critical to understanding
human disease and developing new therapies.
There are an estimated 400 - 500
kinases in the
human genome, with literally dozens being activated during disease processes.
This collaborative project between industrial and academic scientists will continue to expand the KCGS with the goal of fully covering all
human protein
kinases.
There are about 500
kinases in the
human genome, each of which represents a potentially important drug target.
The sequence similarity between MAD - 3 and pp40 includes a casein
kinase II and consensus tyrosine phosphorylation site, as well as five repeats of a sequence found in the
human erythrocyte protein ankyrin.
«About 2 percent, or nearly 500, of all
human genes are dedicated to coding protein
kinases and over 50 percent of
kinases are linked to various
human diseases.»
It is no surprise, then, that having faulty protein
kinases may lead to a number of
human conditions, including cardiovascular diseases, cancer and diabetes.
In experiments with mouse and
human hair follicles, Angela M. Christiano, PhD, and colleagues found that drugs that inhibit the Janus
kinase (JAK) family of enzymes promote rapid and robust hair growth when directly applied to the skin.
Kim and colleagues are interested in studying the activation mechanism of protein
kinase G I (PKG I) because a mutation of PKG I has been shown to cause thoracic aortic disease, as Kim and his collaborators showed in a previous publication in the American Journal of
Human Genetics.
To explore this question, the researchers examined the neurological impact of two enzymes that phosphorylate eIF2alpha,
kinases termed PERK and GCN2, in different populations of AD model mice — all of which expressed genetic mutations akin to those carried by
humans with AD.
But whether p38 MAP
kinase inhibitors could be used to treat arthritis in
humans is unclear, she says.
Rho -
kinase inhibitor Y - 27632 and hypoxia synergistically enhance chondrocytic phenotype and change the S100 protein profile in
human chondrosarcoma cells
↵ 3 The abbreviations used are: HUVEC,
human umbilical vein endothelial cell; DiI - Ac - LDL, 1,1 ′ - dioctadecyl - 3,3,3 ′, 3 ′ - tetramethyl - indocarbocyanine acetylated low - density lipoprotein; FACS, fluorescence - activated cell sorting; FGFR, fibroblast growth factor receptor; Flk, fetal liver
kinase; ICAM, intercellular adhesion molecule; mAb, monoclonal antibody; PE, phycoerythrin; TNF, tumor necrosis factor; VCAM, vascular cell adhesion molecule.
For
human controls these were Excision repair cross-complementing group 3 (ERCC3), Amplified in osteosarcoma (OS - 9), and Casein
kinase - 1d (CSNK1D).
The Monash BDI researchers worked in collaboration with Canadian - based company Kinexus, and used an antibody microarray to simultaneously investigate hundreds of factors involved in cell signalling that were modulated by HCV replication, including
human protein
kinases.
Rho -
kinase inhibitor Y - 27632 increases cellular proliferation and migration in
human foreskin fibroblast cells
This thesis primarily investigates the effects of mechanical cyclic stretching, a 5 % low oxygen atmosphere and the Rho -
kinase inhibitor, Y - 27632, on protein responses in chondrocytic
human chondrosarcoma (HCS - 2 / 8) cells.
In 2005, Cagan's team created a general fly model of a
human thyroid tumor caused by mutations in the Ret receptor tyrosine
kinase gene, then screened a panel of drugs including a
kinase inhibitor called vandetanib that suppressed the tumor (Cancer Res, 65:3538 - 41, 2005).
In their latest research, the Joslin team performed many experiments to explore the actions of these two proteins, called centromere protein A (CENP - A) and polo - like
kinase - 1 (PLK1), in mice and in cells from
humans and mice.
Clough BH, Zeitouni S, Krause U, et al., Rapid Osteogenic Enhancement of Stem Cells in
Human Bone Marrow Using a Glycogen ‐ Synthease ‐
Kinase ‐ 3 ‐ Beta Inhibitor Improves Osteogenic Efficacy In Vitro and In Vivo.
Effect of Saturated Stearic Acid on MAP
Kinase and ER Stress Signaling Pathways during Apoptosis Induction in
Human Pancreatic ß - Cells Is Inhibited by Unsaturated Oleic Acid.
The
human protein
kinase HIPK2 phosphorylates and downregulates the methyl - binding transcription factor ZBTB4.
(h)
Human phospho - receptor tyrosine
kinase array for EphA2, EphB2 and EphB4 ephrin receptors from control BP (shCtr) and BP silenced for Tie2 (siTie2 I and siTie2 II).
Platelet - activating factor - mediated endosome formation causes membrane translocation of p67phox and p40phox that requires recruitment and activation of p38 MAPK, Rab5a, and phosphatidylinositol 3 -
kinase in
human neutrophils.
Miniaturizing each individual experiment allows us to print whole libraries on a single plate, for instance gRNA / siRNA targeting all
kinases in the
human genome are printed on approximately 2.06 cm2 (0.32 sq. in.).
Cellular entry of
human papillomavirus type 16 involves activation of the phosphatidylinositol 3 -
kinase / Akt / mTOR pathway and inhibition of autophagy.
Hunter and his colleague Gerard Manning discovered that the
human genome contains quite a few dead
kinases whose sequences have nonetheless been carefully preserved.
Human phospho - receptor tyrosine
kinase array was performed according to the manufacturer's instructions (R&D, #ARY001B).
Molecular interaction and functional regulation of ClC - 3 by Ca2 + / calmodulin - dependent protein
kinase II (CaMKII) in
human malignant glioma.
Anastellin, a fragment of the first type III repeat of fibronectin, inhibits extracellular signal - regulated
kinase and causes G1 arrest in
human microvessel endothelial cells.
The protein
kinase B - RAF is mutated in approximately 8 % of
human cancers.
Pim - 3, a Proto - Oncogene with Serine / Threonine
Kinase Activity, Is Aberrantly Expressed in
Human Pancreatic Cancer and Phosphorylates Bad to Block Bad - Mediated Apoptosis in
Human Pancreatic Cancer Cell Lines
Confocal images of P150 dystrophic retina transplanted with hNPCctx — GDNF and double stained with antibodies against
human nuclear antigen (red) and either (A) recoverin, a photoreceptor and cone bipolar cell marker (green), or (B) protein
kinase Cα (PKCα), a bipolar cell marker (green).
I wanted to inactivate the gene BRAF (a
kinase implicated in several
human cancers) in A549 cells (a
human lung cancer cell line), armed only with viruses obtained through Addgene's viral service and the methods sections of scientific articles (gasp).
Currently, 31 tyrosine
kinase inhibitors are FDA approved for
human therapy, with many more in clinical trials.
(a
kinase implicated in several
human cancers) in A549 cells (a
human lung cancer cell line), armed only with viruses obtained through Addgene's viral service and the methods sections of scientific articles (gasp).
Enhanced Expression of Myristoylated Alanine — Rich C
Kinase Substrate (MARCKS) in Airway Epithelium of an Animal Model of Allergic Airway Inflammation and
Human Patients with COPD
Inactivation of ABL
kinases inhibited the expression of the TAZ target gene AXL, which shows increased expression in several
human cancers and correlates with poor prognosis, increased invasiveness and metastasis, and enhanced drug resistance (53, 54).
A self - inactivating lentiviral construct containing a mouse phosphoglycerate
kinase - 1 internal promoter driving the
human gene encoding GDNF [44] was used to generate GDNF - secreting hNPCctx.
ABL tyrosine
kinases play an oncogenic role in
human leukemias (4, 5) and promote the progression of solid tumors (5, 6).
University of Wisconsin A chemical - genetic library of
human cell lines for evaluating pharmacologic inhibition of protein
kinases
Flavopiridol inhibits several cellular
kinases and has demonstrated cytostatic and cytotoxic activity in vitro and in vivo in numerous
human tumor cell lines and xenograft models (including
human breast, prostate, and lung carcinoma) at clinically achievable concentrations.
Prediction of the structure of
human Janus
kinase 2 (JAK2) comprising the two carboxy - terminal domains reveals a mechanism for autoregulation
At that time researchers had only just begun to understand the 58 tyrosine
kinases in the
human proteome, of which EGFR is one.