• 3' Phosphatase activity toward phosphatidylinositol 3,4-bisphosphate [PI(3,4)P2] by voltage-sensing phosphatase (VSP)
• 46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)
• A mutant form of PTEN linked to autism
• A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas
• A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia
• A novel RING finger-B box-coiled-coil protein, GERP
• A voltage-sensing phosphatase, Ci-VSP, which shares sequence identity with PTEN, dephosphorylates phosphatidylinositol 4,5-bisphosphate
• Alleles in chromosome 10p21-26 in malignant gliomas
• Allosteric activation of PTEN phosphatase by phosphatidylinositol 4,5-bisphosphate
• An E3 ubiquitin ligase, Really Interesting New Gene (RING) Finger 41, is a candidate gene for anxiety-like behavior and beta-carboline-induced seizures
• Centromere activation
• Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia
• Chromosome r(10)(p15.3q26.12) in a newborn child: case report
• Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3
• Clinical, cytogenetic and molecular study of a case of ring chromosome 10
• Cloning, genetic mapping and expression studies of the rat Brca1 gene
• Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis
• Constitutional ring chromosomes and tumour suppressor genes
• Cytogenetic aberrations in osteosarcomas. Nonrandom deletions, rings, and double-minute chromosomes
• DCAF13 promotes triple-negative breast cancer metastasis by mediating DTX3 mRNA degradation
• Deletion of the short arm of chromosome 10 (10p13): report of a patient and review
• Deletions of the long arm of chromosome 10
• Development of spectral colour banding in cytogenetic analysis
• Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14
• Epigenetic markers of prostate cancer in plasma circulating DNA
• Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index
• Expanding the Neurological Phenotype of Ring Chromosome 10 Syndrome: A Case Report and Review of the Literature
• First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature
• From spermatocytes to sperm: meiotic behaviour of human male reciprocal translocations
• Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria
• Identification of loci and candidate gene GmSPX-RING1 responsible for phosphorus efficiency in soybean via genome-wide association analysis
• Imputation of genotypes from low density (50,000 markers) to high density (700,000 markers) of cows from research herds in Europe, North America, and Australasia using 2 reference populations
• Inhibiting PTEN
• Is chromosome 10 a primary chromosomal abnormality in endometrial adenocarcinoma?
• Large-Scale Conformational Transitions in Supercoiled DNA Revealed by Coarse-Grained Simulation
• Lipid phosphatases in the regulation of T cell activation: living up to their PTEN-tial
• Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy
• Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome
• Metabolic switching of PI3K-dependent lipid signals
• MicroRNA-300 Regulates the Ubiquitination of PTEN through the CRL4B^DCAF13 E3 Ligase in Osteosarcoma Cells
• Modeling PTEN overexpression-induced microcephaly in human brain organoids
• Molecular distinction between true centric fission and pericentric duplication-fission
• Molecular genetic analysis of anaplastic pleomorphic xanthoastrocytoma
• Myxoinflammatory fibroblastic sarcoma with complex supernumerary ring chromosomes composed of chromosome 3 segments
• Myxoinflammatory fibroblastic sarcoma: morphologic and genetic updates
• Novel genes as primary triggers for polygenic hypertension
• Novel inhibitors of the PI3K family
• Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease
• Phenotype associated with ring 10 chromosome: report of patient and review of literature
• Phosphatidylinositol 3-kinase inhibitors: promising drug candidates for cancer therapy
• Phosphoinositide phosphatases in a network of signalling reactions
• Physical retardation is associated with ring chromosome mosaicism: 46, XX,r(10)/45, XX,10 minus
• Polyceraty (multi-horns) in Damara sheep maps to ovine chromosome 2
• Post-mortem studies on two patients with 1-2 band cytogenetic deletions: 10q26----qter and r(9)(p24q34)
• Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
• Promoter methylation and silencing of PTEN in gastric carcinoma
• PTEN phosphatase selectively binds phosphoinositides and undergoes structural changes
• Pure trisomy 10p resulting from an extra ring chromosome: characterization by methods of advanced molecular cytogenetics
• Recurrent involvement of ring-type zinc finger genes in complex molecular rearrangements in childhood acute myelogeneous leukemia with translocation t(10;11)(p12;q23)
• Report of a patient with a ring chromosome 10: mos45,XY,-10/46,XY/46,XY,r(10)(p15.3q26.3)
• Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13
• Ring 10 chromosome: 46,XX,r10(p15q26)
• Ring chromosome 10 (p15q26) in a patient with unipolar affective disorder, multiple minor anomalies, and mental retardation
• Ring chromosome 10 and its clinical features
• Ring chromosome 10 associated with multiple congenital malformations
• Ring Chromosome 10 in a Case of Acute Promyelocytic Leukemia
• Ring chromosome 10 syndrome: case report and the possibility of clinical diagnosis
• Ring chromosome 10: 46,XX,r(10)(p15q26)
• Ring chromosome 10: report on two patients and review of the literature
• Ring chromosome 10:46,XX,r(10)(p15 leads to q26)
• SHIP-2 and PTEN are expressed and active in vascular smooth muscle cell nuclei, but only SHIP-2 is associated with nuclear speckles
• Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH
• Small molecule TSC01682 inhibits osteosarcoma cell growth by specifically disrupting the CUL4B-DDB1 interaction and decreasing the ubiquitination of CRL4B E3 ligase substrates
• Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype
• Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas
• Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant mice
• Supernumerary ring marker chromosome as a secondary rearrangement in a parapharyngeal lipoma with t(10;12)(q25;q15) as the primary karyotypic abnormality
• The Function of Inositol Phosphatases in Plant Tolerance to Abiotic Stress
• The protein-protein interaction-mediated inactivation of PTEN
• TRIM8: Making the Right Decision between the Oncogene and Tumour Suppressor Role
• Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions
• Ubiquitin ligase MARCH8 promotes the malignant progression of hepatocellular carcinoma through PTEN ubiquitination and degradation
• Urocanic acid-modified chitosan-mediated PTEN delivery via aerosol suppressed lung tumorigenesis in K-ras(LA1) mice