| scholarly article | Q13442814 |
| P50 | author | Felice Tirone | Q37374268 |
| P2093 | author name string | Matsas R | |
| Mamalaki A | |||
| Georgopoulou N | |||
| Pappa C | |||
| Gaitanou M | |||
| Buanne P | |||
| P2860 | cites work | Identification of a novel p53 functional domain that is necessary for efficient growth suppression | Q24311276 |
| Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15 | Q24568014 | ||
| Genomic sequencing | Q24594942 | ||
| Gene discovery in dbEST. | Q48078968 | ||
| Postnatal development of the cerebellar cortex in the rat. I. The external germinal layer and the transitional molecular layer | Q48751146 | ||
| Purification and Characterization of Neuron-Specific Surface Antigen Defined by Monoclonal Antibody BM88 | Q48789082 | ||
| Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1. | Q52182653 | ||
| MN20, a D2 cyclin, is transiently expressed in selected neural populations during embryogenesis. | Q52203964 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia | Q57287881 | ||
| Tumour-suppressor activity of H19 RNA | Q59071440 | ||
| Neuron- and myelin-specific monoclonal antibodies recognizing cell-surface antigens of the central and peripheral nervous system | Q69657232 | ||
| Allele loss at the c-Ha-ras1 locus in human ovarian cancer | Q69947887 | ||
| Monoclonal antibodies to mammalian neurofilaments | Q70187733 | ||
| Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5. | Q71668047 | ||
| Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3 | Q71862688 | ||
| Characterization and localization of the BM88 antigen in the developing and adult rat brain | Q71896557 | ||
| Parental genomic imprinting of the human IGF2 gene | Q72222239 | ||
| Early expression of the BM88 antigen during neuronal differentiation of P19 embryonal carcinoma cells | Q73544944 | ||
| The N terminus of the murine p53 tumour suppressor is an independent regulatory domain affecting activation and thermostability | Q74186440 | ||
| Loss of DCC expression in neuroblastoma is associated with disease dissemination | Q77557199 | ||
| Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction | Q25938986 | ||
| Basic local alignment search tool | Q25938991 | ||
| Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs | Q27860573 | ||
| Protein modules and signalling networks | Q27860694 | ||
| CDK inhibitors: positive and negative regulators of G1-phase progression | Q27860983 | ||
| The DCC gene product in cellular differentiation and colorectal tumorigenesis | Q28238617 | ||
| Genomic imprinting of a human apoptosis gene homologue, TSSC3 | Q28264509 | ||
| A 1.4-Mb high-resolution physical map and contig of chromosome segment 11p15.5 and genes in the LOH11A metastasis suppressor region | Q28296418 | ||
| RETRACTED: The TSG101 tumor susceptibility gene is located in chromosome 11 band p15 and is mutated in human breast cancer | Q28302841 | ||
| Modular binding domains in signal transduction proteins | Q29617351 | ||
| Structural basis for the binding of proline-rich peptides to SH3 domains | Q29620408 | ||
| The morbid anatomy of the human genome: chromosomal location of mutations causing disease | Q30495387 | ||
| Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells | Q30501796 | ||
| Apoptosis and cell division | Q33923835 | ||
| DNA sequencing with chain-terminating inhibitors. 1977. | Q34258273 | ||
| Differential DNA sequence deletions from chromosomes 3, 11, 13, and 17 in squamous-cell carcinoma, large-cell carcinoma, and adenocarcinoma of the human lung | Q34287423 | ||
| A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci | Q35194082 | ||
| Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. | Q35248366 | ||
| Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. | Q35248407 | ||
| Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer | Q35477427 | ||
| Chromosomal localisation of two putative 11p oncosuppressor genes involved in human ovarian tumours | Q35994651 | ||
| Identifying and manipulating neuronal stem cells | Q36705255 | ||
| Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas | Q36976941 | ||
| Molecular cloning and biological activity of a novel developmentally regulated gene encoding a protein with beta-transducin-like structure | Q38309094 | ||
| The origins of cellular diversity in the mammalian central nervous system | Q38688069 | ||
| Report of the committee on structural chromosome changes in neoplasia | Q38695779 | ||
| Adhesion molecules and the hierarchy of neural development | Q39584231 | ||
| Neuronal migration, with special reference to developing human brain: a review | Q39880021 | ||
| Glial cell line-derived neurotrophic factor and developing mammalian motoneurons: regulation of programmed cell death among motoneuron subtypes. | Q40872041 | ||
| Co-localization of the glial cell-line derived neurotrophic factor and its functional receptor c-RET in a subpopulation of rat dorsal root ganglion neurons | Q40919142 | ||
| Overexpression of the neuron-specific molecule BM88 in mouse neuroblastoma cells: altered responsiveness to growth factors | Q41068061 | ||
| Stem cells in the central nervous system | Q41116811 | ||
| Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay | Q41231379 | ||
| Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndrome | Q41364089 | ||
| Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome | Q41523994 | ||
| Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11. | Q41661378 | ||
| Genes controlling neural fate and differentiation. | Q41670077 | ||
| Role of the von Hippel-Lindau tumor suppressor protein during neuronal differentiation | Q41741006 | ||
| Postnatal development of the cerebellar cortex in the rat. II. Phases in the maturation of Purkinje cells and of the molecular layer | Q43825550 | ||
| The BM88 antigen, a novel neuron-specific molecule, enhances the differentiation of mouse neuroblastoma cells. | Q48072903 | ||
| P433 | issue | Pt 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Cell cycle exit and neuronal differentiation 1 | Q21131293 |
| Beckwith-Wiedemann syndrome | Q521863 | ||
| P304 | page(s) | 715-724 | |
| P577 | publication date | 2001-05-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis | |
| P478 | volume | 355 |
| Q36140588 | BM88/CEND1 coordinates cell cycle exit and differentiation of neuronal precursors |
| Q66680403 | Cend1, a Story with Many Tales: From Regulation of Cell Cycle Progression/Exit of Neural Stem Cells to Brain Structure and Function |
| Q35060879 | Functional Interactions between BM88/Cend1, Ran-binding protein M and Dyrk1B kinase affect cyclin D1 levels and cell cycle progression/exit in mouse neuroblastoma cells |
| Q34017774 | The 4C5 cell-impermeable anti-HSP90 antibody with anti-cancer activity, is composed of a single light chain dimer |
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