about
Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduriaIminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transportersHartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19Targeting ASCT2-mediated glutamine uptake blocks prostate cancer growth and tumour developmentMonoterpene glycoside ESK246 from Pittosporum targets LAT3 amino acid transport and prostate cancer cell growth.Inositol polyphosphate 4-phosphatase II regulates PI3K/Akt signaling and is lost in human basal-like breast cancersLuciferase expression and bioluminescence does not affect tumor cell growth in vitro or in vivo.Persistence of the common Hartnup disease D173N allele in populations of European origin.Targeted inactivation of dipeptidyl peptidase 9 enzymatic activity causes mouse neonate lethality.Identification of P-Rex1 as a novel Rac1-guanine nucleotide exchange factor (GEF) that promotes actin remodeling and GLUT4 protein trafficking in adipocytesRBM3 regulates temperature sensitive miR-142-5p and miR-143 (thermomiRs), which target immune genes and control fever.ASCT2/SLC1A5 controls glutamine uptake and tumour growth in triple-negative basal-like breast cancer.The antiproliferative ELF2 isoform, ELF2B, induces apoptosis in vitro and perturbs early lymphocytic development in vivoCTCF and BORIS in genome regulation and cancer.Phosphatidylinositol 3-phosphate [PtdIns3P] is generated at the plasma membrane by an inositol polyphosphate 5-phosphatase: endogenous PtdIns3P can promote GLUT4 translocation to the plasma membrane.The cancer-testis antigen BORIS phenocopies the tumor suppressor CTCF in normal and neoplastic cells.Androgen receptor and nutrient signaling pathways coordinate the demand for increased amino acid transport during prostate cancer progression.OCT-1 function varies with cell lineage but is not influenced by BCR-ABL.PtdIns(3,4,5)P3-dependent Rac Exchanger 1 (PREX1) Rac-Guanine Nucleotide Exchange Factor (GEF) Activity Promotes Breast Cancer Cell Proliferation and Tumor Growth via Activation of Extracellular Signal-regulated Kinase 1/2 (ERK1/2) Signaling.CTCF genetic alterations in endometrial carcinoma are pro-tumorigenic.Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria.Orchestrated intron retention regulates normal granulocyte differentiation.High-throughput clonal selection of recombinant CHO cells using a dominant selectable and amplifiable metallothionein-GFP fusion protein.Targeting amino acid transport in metastatic castration-resistant prostate cancer: effects on cell cycle, cell growth, and tumor development.Targeting glutamine transport to suppress melanoma cell growth.Regulation of Fc R-stimulated phagocytosis by the 72-kDa inositol polyphosphate 5-phosphatase: SHIP1, but not the 72-kDa 5-phosphatase, regulates complement receptor 3 mediated phagocytosis by differential recruitment of these 5-phosphatases to the pMolecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathyLoss of solute carriers in T cell-mediated rejection in mouse and human kidneys: an active epithelial injury-repair response
P50
Q24310676-29A2CEDE-77C2-4100-A532-12FCFF7BA847Q24317890-85B12CAA-2FEA-4F12-96A9-6AC74675BF8FQ28275118-D83611BC-F9E9-47E0-930B-1950424D5A57Q28831339-B6BDC61C-E961-4D71-B603-1E94A03BE89DQ33797210-9C2D1047-3952-4D30-AF9E-65F6175FD649Q34153121-9E816773-3497-45F0-A6B4-97B3392E6B23Q34410549-F45BDD34-3001-4D72-811D-4E0870EE0848Q34635430-59BE2481-A8D8-43AD-AC13-DA7A5C067802Q35040181-F559EAF4-0ACC-48FB-A51B-9336DDEA45D0Q35604609-64D52B5F-6AF5-44A2-91C4-D9A41C8EE0E5Q36775559-C92B6870-388E-4818-9F0D-C82A02F9F07DQ37023688-F4B7BDDA-7BA6-41BC-B19F-C3F8896CB3A3Q37727031-982624DD-A735-4A70-9EA5-559BB8C880D3Q38198427-32EE2536-7DB4-484B-87D1-7D5418BB6A3FQ38409013-8FDBE46D-6E44-41E1-AA8E-CDD37DD8F9C1Q39172013-F23835BD-40B7-4252-A076-B1D846031FE1Q39456571-B674DB7F-29D3-433F-99C7-2D49CF93ECFDQ39640517-2698F4E6-A392-47AA-8AF0-A982BBE5CEE7Q41045830-2D0302AD-8BB2-4367-920C-905E46ADE162Q41073866-0892C95F-6A69-4081-B641-3ABFE6CBB62DQ43106088-A7BAF330-1D5D-43AC-B928-5DDFB1A4F4CEQ47870903-5F4DB996-82F4-4F56-B96C-BD888D764F6FQ51842465-6A4DEC82-9495-44EC-8A18-C979777897DEQ53089488-822EF88A-B990-4F14-A0B8-BF193BEA7DBAQ54376941-3ACF3516-516F-49BA-B8FE-E71FFEB3FD58Q63681815-16771AEB-02DE-40AF-945A-11706FC37B10Q80207338-242F7E4E-C061-460F-916E-3E16AEFC78EAQ85114918-B22CC7E1-5F2C-44CA-BB1B-A3E1B47322EE
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Charles G Bailey
@es
Charles G Bailey
@nl
Charles G Bailey
@sl
Charles G. Bailey
@en
type
label
Charles G Bailey
@es
Charles G Bailey
@nl
Charles G Bailey
@sl
Charles G. Bailey
@en
prefLabel
Charles G Bailey
@es
Charles G Bailey
@nl
Charles G Bailey
@sl
Charles G. Bailey
@en
P106
P1153
36184951400
P21
P31
P496
0000-0002-4725-7829