Denise Sheer | Academic Influence

Denise Sheer's AcademicInfluence.com Rankings

Denise Sheer

Biology

#3803

World Rank

#5762

Historical Rank

Genetics

#965

World Rank

#1061

Historical Rank

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Biology

Denise Sheer's Degrees

PhD Genetics Stanford University
Masters Biology Stanford University
Bachelors Biology University of California, Berkeley

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Why Is Denise Sheer Influential?

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According to Wikipedia, Denise Sheer was appointed professor of human genetics at The Institute of Cell and Molecular Science at Queen Mary, University of London in November 2006. Her fields of expertise include cell and molecular biology; cancer genetics and epigenetics; and molecular pathology of paediatric brain tumours.

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Denise Sheer's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Localization of the gene for familial adenomatous polyposis on chromosome 5 (1987) (1379)
The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts. (1994) (1043)
Plasticity in the organization and sequences of human KIR/ILT gene families. (2000) (665)
Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas (2013) (655)
Molecular analysis of acute promyelocytic leukemia breakpoint cluster region on chromosome 17. (1990) (626)
Combinatorial generation of variable fusion proteins in the Ewing family of tumours. (1993) (539)
Large-scale chromatin organization of the major histocompatibility complex and other regions of human chromosome 6 and its response to interferon in interphase nuclei. (2000) (477)
The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis (1999) (393)
The Human Polycomb Group Complex Associates with Pericentromeric Heterochromatin to Form a Novel Nuclear Domain (1998) (284)
Activation of the ERK/MAPK pathway: a signature genetic defect in posterior fossa pilocytic astrocytomas (2009) (272)
Comparative genomic hybridization of breast tumors stratified by histological grade reveals new insights into the biological progression of breast cancer. (1999) (269)
Promyelocytic leukemia nuclear bodies associate with transcriptionally active genomic regions (2004) (236)
Isolation of cDNA clones encoding the beta isozyme of human DNA topoisomerase II and localisation of the gene to chromosome 3p24. (1992) (233)
Subchromosomal positioning of the epidermal differentiation complex (EDC) in keratinocyte and lymphoblast interphase nuclei. (2002) (217)
Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoire. (1994) (206)
Molecular cloning and tissue expression of FAT, the human homologue of the Drosophila fat gene that is located on chromosome 4q34-q35 and encodes a putative adhesion molecule. (1995) (170)
Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome (1983) (162)
Characterisation of human thyroid epithelial cells immortalised in vitro by simian virus 40 DNA transfection. (1989) (162)
Proteasome components with reciprocal expression to that of the MHC-encoded LMP proteins (1994) (159)
Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia. (1997) (149)
Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization. (1994) (147)
Chromosomal localisation of the human homologues to the oncogenes erbA and B. (1984) (146)
LIM–kinase deleted in Williams syndrome (1996) (145)
PML bodies associate specifically with the MHC gene cluster in interphase nuclei. (2001) (145)
The role of microhomology in genomic structural variation. (2014) (143)
The isolation and characterization of colorectal epithelial cell lines at different stages in malignant transformation from familial polyposis coli patients (1984) (134)
Molecular cloning of human lysyl oxidase and assignment of the gene to chromosome 5q23.3-31.2. (1991) (125)
Molecular and Phenotypic Characterisation of Paediatric Glioma Cell Lines as Models for Preclinical Drug Development (2009) (115)
The hypervariable gene locus PUM, which codes for the tumour associated epithelial mucins, is located on chromosome 1, within the region 1g21–24 (1987) (114)
Allelic loss at SMAD4 in polyps from juvenile polyposis patients and use of fluorescence in situ hybridization to demonstrate clonal origin of the epithelium. (2000) (111)
Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus. (1990) (108)
Chromosomal mapping of the human and mouse homologues of two new members of the AP-2 family of transcription factors. (1996) (100)
MAPK pathway activation and the origins of pediatric low‐grade astrocytomas (2009) (97)
Type 5 acid phosphatase. Sequence, expression and chromosomal localization of a differentiation-associated protein of the human macrophage. (1990) (95)
The role of nuclear organization in cancer (2010) (89)
Transformation associated p53 protein is encoded by a gene on human chromosome 17 (1985) (88)
Characterization and chromosomal assignment of a human cell surface antigen defined by the monoclonal antibody AUAI (1986) (87)
Purification and composition of the human tumor-associated glycoprotein (TAG-72) defined by monoclonal antibodies CC49 and B72.3. (1988) (87)
Tumour angiogenesis is reduced in the Tc1 mouse model of Down Syndrome (2010) (86)
P-STAT1 mediates higher-order chromatin remodelling of the human MHC in response to IFNγ (2007) (82)
Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q. (1996) (81)
Diagnosis of Ewing's sarcoma and peripheral neuroectodermal tumour based on the detection of t(11;22) using fluorescence in situ hybridisation. (1993) (80)
CD164, a novel sialomucin on CD34(+) and erythroid subsets, is located on human chromosome 6q21. (1998) (74)
A role for SC35 and hnRNPA1 in the determination of amyloid precursor protein isoforms (2007) (71)
Establishment and characterisation of three new human ovarian carcinoma cell lines and initial evaluation of their potential in experimental chemotherapy studies (1987) (69)
Genomic Profiling Identifies Discrete Deletions Associated with Translocations in Glioblastoma Multiforme (2006) (67)
Anchoring the genome (2008) (63)
RAF gene fusion breakpoints in pediatric brain tumors are characterized by significant enrichment of sequence microhomology. (2011) (62)
The human homologue of the mouse t‐complex gene, TCP1, is located on chromosome 6 but is not near the HLA region. (1987) (62)
Regional localization of the gene coding for human brain nitric oxide synthase (NOS1) to 12q24.2-->24.31 by fluorescent in situ hybridization. (1993) (61)
Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13. (1990) (60)
Cloning and chromosome mapping of the human interleukin-1 receptor antagonist gene. (1992) (59)
The human placental alkaline phosphatase gene and related sequences map to chromosome 2 band q37 (1987) (57)
Catalog of chromosome aberrations in cancer (5th edn): by Felix Mitelman (Bertil Johansson and Fredrik Mertens associated eds) Wiley-Liss, 1994. £345.00 $518.00 (xxi + 4252 pages; 2 volumes) ISBN 0 471 11183 X (1995) (57)
Mapping of the genes encoding human inducible and endothelial nitric oxide synthase (NOS2 and NOS3) to the pericentric region of chromosome 17 and to chromosome 7, respectively. (1994) (56)
The homeobox gene MEIS1 is amplified in IMR-32 and highly expressed in other neuroblastoma cell lines. (2000) (56)
MYB upregulation and genetic aberrations in a subset of pediatric low-grade gliomas (2010) (56)
Microglia promote glioblastoma via mTOR‐mediated immunosuppression of the tumour microenvironment (2020) (54)
Released chromatin: linearized DNA for high resolution fluorescence in situ hybridization. (1994) (54)
Assignment of the gene encoding the beta‐subunit of the human fibronectin receptor (β‐FNR) to chromosome 10p11.2 (1989) (54)
Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome (2010) (53)
Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization. (1993) (52)
RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort (2010) (51)
A testis-expressed Zn finger gene (ZNF76) in human 6p21.3 centromeric to the MHC is closely linked to the human homolog of the t-complex gene tcp-11. (1992) (50)
Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridisation on tumour imprints and bone marrow smears. United Kingdom Children's Cancer Study Group. (1994) (49)
Genetic analysis of the 15;17 chromosome translocation associated with acute promyelocytic leukemia. (1983) (49)
Cytogenetic analysis of four human ovarian carcinoma cell lines. (1987) (46)
Mini review: Form and function in the human interphase chromosome (2000) (46)
A monoclonal antibody recognizing a cell surface antigen coded for by a gene on human chromosome 17 (1982) (44)
Fusion of the EWS Gene to a DNA segment from 9q22‐31 in a human myxoid chondrosarcoma (1995) (43)
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli. (1989) (42)
Molecular cloning and analysis of the fragile X region in man. (1991) (38)
Analysis of NotI linking clones isolated from human chromosome 3 specific libraries. (1999) (38)
Construction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transfer. (1988) (37)
Biochemical and genetic analysis of the Oka blood group antigen (2004) (37)
Chromosomal localization, gene structure and transcription pattern of the ORFX gene, a homologue of the MHC-linked RING3 gene. (1997) (37)
Monosomy 7 and multipotential stem cell transformation (1985) (36)
Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-κB pathways (2015) (36)
Recruitment of Heterogeneous Nuclear Ribonucleoprotein A1in Vivo to the LMP/TAP Region of the Major Histocompatibility Complex* (2003) (36)
H-RYK, an Unusual Receptor Kinase: Isolation and Analysis of Expression in Ovarian Cancer (1996) (32)
Satellite DNA binding and cellular localisation of RNA helicase P68 (2005) (31)
Localization of the oncogene c‐erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17 (1985) (31)
Generation of a genomic tiling array of the human Major Histocompatibility Complex (MHC) and its application for DNA methylation analysis (2008) (30)
Non‐random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping (2001) (30)
The small cell lung cancer antigen cluster-4 and the leukocyte antigen CD24 are allelic isoforms of the same gene (CD24) on chromosome band 6q21. (1995) (30)
Molecular analysis of simple variant translocations in acute promyelocytic leukemia (1994) (30)
Reconfiguration of genomic anchors upon transcriptional activation of the human major histocompatibility complex. (2008) (29)
Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193. (1997) (28)
Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumor propagation in vitro. (2013) (28)
Genomic structure and domain organisation of the human Bak gene. (1998) (28)
Deletion of part of the short arm of chromosome 17 in a congenital fibrosarcoma. (1990) (27)
Assignment and Ordering of Twenty-Three Unique Notl-Linking Clones Containing Expressed Genes Including the Guanosine 5′-Monophosphate Synthetase Gene to Human Chromosome 3 (1997) (27)
The organization and conservation of the human Surfeit gene cluster and its localization telomeric to the c-abl and can proto-oncogenes at chromosome band 9q34.1. (1993) (27)
Localization of the genes encoding the catalytic subunits of protein phosphatase 2A to human chromosome bands 5q23-->q31 and 8p12-->p11.2, respectively. (1993) (26)
Widespread Expression of BORIS/CTCFL in Normal and Cancer Cells (2011) (24)
A cDNA encoding a muscle-type tropomyosin cloned from a human epithelial cell line: identity with human fibroblast tropomyosin TM1. (1991) (24)
Conditional immortalization of human thyroid epithelial cells: a tool for analysis of oncogene action (1990) (24)
Chromosomal localisation of the human envoplakin gene (EVPL) to the region of the tylosis oesophageal cancer gene (TOCG) on 17q25. (1996) (24)
The ubiquitin-homology gene PIC1: characterization of mouse (Pic1) and human (UBL1) genes and pseudogenes. (1998) (23)
Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping. (2001) (22)
Confirmation that the Type I collagen gene on chromosome 17 is COL1A1 (α1(I)), using a human genomic probe (1984) (21)
Fluorescence in situ hybridization techniques for the rapid detection of genetic prognostic factors in neuroblastoma (2000) (21)
Localisation of the gene encoding the catalytic gamma subunit of phosphorylase kinase to human chromosome bands 7p12-q21. (1990) (21)
Cytogenetic analysis of primitive neuroectodermal tumors. Absence of the t(11;22) in two of three cases and a review of the literature. (1991) (21)
HnRNP-A1 binds directly to double-stranded DNA in vitro within a 36 bp sequence (2004) (20)
Regional assignment of the human gene coding for a multifunctional polypeptide (P4HB) acting as the beta-subunit of prolyl 4-hydroxylase and the enzyme protein disulfide isomerase to 17q25. (1991) (19)
The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI). (1998) (18)
Assignment of the gene coding for the alpha-subunit of prolyl 4-hydroxylase to human chromosome region 10q21.3-23.1. (1989) (18)
Isolation of probes specific to human chromosomal region 6p21 from immunoselected irradiation-fusion gene transfer hybrids. (1991) (18)
Genetic relationships of the genes encoding the human proteasome beta subunits and the proteasome PA28 complex. (1997) (17)
DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas (2016) (16)
Karyotypic analysis of the human monoblastic cell line U937. (1988) (16)
Localization of the Surfeit gene cluster containing the ribosomal protein gene L7a to chromosome bands 9q33‐34. (1989) (16)
Localization of the oncogene c‐erbA2 to human chromosome 3 (1987) (16)
The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12-p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2. (1995) (15)
The proteome of neurofilament-containing protein aggregates in blood (2018) (15)
The human LFA-3 gene is located at the same chromosome band as the gene for its receptor CD2 (2004) (15)
Cohesion, but not too close (2001) (15)
A novel and rapid method for isolating sequences adjacent to rare cutting sites and their use in physical mapping. (1991) (15)
The human dendritic cell marker CD83 maps to chromosome 6p23 (1999) (15)
Clinical applications of genetic rearrangements in cancer. (1996) (14)
CTCF binds to sites in the major histocompatibility complex that are rapidly reconfigured in response to interferon-gamma (2012) (14)
The genetic analysis of prostate carcinoma. (1997) (14)
The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridization. (1994) (13)
Assignment of the human creatine transporter type 2 (SLC6A10) to chromosome band 16p11.2 by in situ hybridization. (1997) (13)
Narrowing of the region of allelic loss in 21q11‐21 in squamous non‐small cell lung carcinoma and cloning of a novel ubiquitin‐specific protease gene from the deleted segment (2000) (13)
Fine Mapping of Probes in the Adenomatous Polyposis Coli Region of Chromosome 5 by In Situ Hybridization (1991) (13)
Ordering of probes surrounding the Ewing's sarcoma breakpoint on chromosome 22 using fluorescent in situ hybridization to interphase nuclei. (1993) (13)
Enzymatic degradation of RNA causes widespread protein aggregation in cell and tissue lysates (2019) (13)
The CL100 gene, which encodes a dual specificity (Tyr/Thr) MAP kinase phosphatase, is highly conserved and maps to human chromosome 5q34 (1994) (13)
Assignment of the human and mouse LIM-kinase genes (LIMK1; Limk1) to chromosome bands 7q11.23 and 5G1, respectively, by in situ hybridization. (1996) (12)
Incidence of the 15q+;17q- chromosome translocation in acute promyelocytic leukaemia (APL). (1985) (12)
Chromosomal locations of the gene coding for the CD3 (T3) γ subunit of the human and mouse CD3/T-cell antigen receptor complexes (2004) (12)
Gene amplification accompanied by the loss of a chromosome containing the native allele and the appearance of the amplified DNA at a new chromosomal location. (1991) (11)
DNA replication-dependent induction of gene proximity by androgen. (2015) (11)
The gene coding for the p68 calcium-binding protein is localised to bands q32–q34 of human chromosome 5, and to mouse chromosome 11 (1989) (10)
THE HIGH-FREQUENCY RED-CELL ANTIGEN OKA IS CARRIED ON A SERIES OF POLYPEPTIDES OF APPARENT MOLECULAR-WEIGHT RANGING FROM 35KD TO 68KD AND IS CONTROLLED BY A GENE ON CHROMOSOME-19 (1987) (10)
Carcinoembryonic antigen (CEA) expression in somatic cell hybrids (1982) (9)
Mapping of the human SAP1 (SRF accessory protein 1) gene and SAP2, a gene encoding a related protein, to chromosomal bands 1q32 and 12q23, respectively. (1994) (9)
BORIS/CTCFL is an RNA-binding protein that associates with polysomes (2013) (9)
Characterization of a continuous cell line in culture established from a Krukenberg tumour of the ovary arising from a primary gastric adenocarcinoma. (1988) (9)
Molecular Characterization of a cDNA Encoding Functional Human CLK4 Kinase and Localization to Chromosome 4q35 (2001) (9)
A somatic cell hybrid panel for regional mapping of human chromosome 18. (1992) (9)
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification. (1992) (8)
Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line (1999) (8)
Three different brain tumours evolving from a common origin (2013) (8)
c-MYC overexpression induces choroid plexus papillomas through a T-cell mediated inflammatory mechanism (2019) (8)
Is prostate cancer worth diagnosing? (1995) (8)
15/17 chromosome translocation in acute promyelocytic leukemia. (1982) (8)
HIGH GRADE GLIOMAS (2012) (8)
Monosomy 7 and Ph-positive acute lymphoblastic leukaemia: cytogenetic and molecular aspects. (1987) (8)
Comparative epigenetic analysis of tumour initiating cells and syngeneic EPSC-derived neural stem cells in glioblastoma (2021) (7)
Yeast artificial chromosomes for the molecular analysis of the familial polyposis APC gene region. (1992) (7)
Characterization of a t(I0; II) (pI3‐I4; qI4‐2I) in the monoblastic cell line U937 (1995) (7)
RFLP for the human erb-A1 gene. (1986) (7)
A long-range restriction map of human chromosome 5q21-q23. (1993) (7)
Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17. (1989) (6)
SR8--the establishment and characterisation of a new ovarian carcinoma cell line and xenograft model. (1996) (6)
Cloning of the region between HLA-DMB and LMP2 in the human major histocompatibility complex. (1994) (6)
Complex translocation involving Ph chromosome in a patient with typical chronic myelogenous leukemia. (1992) (6)
Replication Timing Profile Reflects the Distinct Functional and Genomic Features of the MHC Class II Region (2007) (6)
Analysis of circulating protein aggregates as a route of investigation into neurodegenerative disorders (2021) (6)
Deletion of c-ets1 and T3γ loci from the 11q- chromosome in the human monoblastic cell line U937 (1989) (5)
Genome-wide methylation analysis identifies genes silenced in non-seminoma cell lines (2016) (5)
Regional sublocalization of the human thyroid peroxidase gene (TPO) by tritium and fluorescence in situ hybridization to chromosome 2p25-->p24. (1993) (5)
The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1p (1987) (5)
ANOTHER RED-CELL SURFACE-ANTIGEN, OKA, IS ENCODED BY A GENE ON CHROMOSOME-19 (1987) (4)
The polymorphic human DNA sequence D8S8 assigned to 8ql3‐21.1, close to the carbonic anhydrase gene cluster, by isotopic and non‐isotopic in situ hybridization and by linkage analysis (1990) (4)
The gene coding for human deoxyhypusine synthase (DHPS) maps to chromosome 19p13.11-p13.12. (1996) (4)
Calendar of Events: 1991 — 1992 (1991) (4)
Characterization of a t(10;11)(p13-14;q14-21) in the monoblastic cell line U937. (1995) (4)
Human Chromosomes (4th Edition) (2001) (4)
Nature GeNetics ADVANCE ONLINE PUBLICATION (2013) (3)
Molecular characterization of a cDNA encoding functional human CLK4 kinase and localization to chromosome 5q35 [correction of 4q35]. (2001) (3)
The human HIV-1 Rev binding-protein hRIP/Rab (HRB) maps to chromosome 2q36. (1997) (3)
"Junction trapping". A simple PCR-based method for the isolation of YAC-insert termini. (1993) (2)
8711 POSTER Addition of Erlotinib Changes Gene Expression in Glioblastoma Cell Lines Treated With Vorinostat (2011) (2)
Deletion of c-ets1 and T3 gamma loci from the 11q- chromosome in the human monoblastic cell line U937. (1989) (2)
cDNA cloning and chromosomal mapping of a mouse gene with homology to NTPases (1998) (2)
c-MYC overexpression induces choroid plexus papillomas through a T-cell mediated inflammatory mechanism (2019) (1)
BORIS/CTCFL is an RNA-binding protein that associates with polysomes (2013) (1)
Cytogenetic analysis of a cell line established from a Krukenberg tumor. (1990) (1)
Genetic mechanisms in carcinogenesis. (1983) (1)
Activation of the MAPK Pathway: A Signature Genetic Defect in Posterior Fossa Pilocytic Astrocytomas (2009) (1)
DNA Methylation Analysis of Paediatric Low-Grade Astrocytomas Identifies a Tumour-Specific Signature at a Set of Enhancers (2015) (1)
Global hypo-methylation in a proportion of glioblastoma enriched for an astrocytic signature is associated with increased invasion and altered immune landscape (2022) (1)
Genetic aspects of carcinogenesis (1985) (1)
Abstracts of the 12th European Colloquium on Cytogenetics of Domestic Animals (1996) (1)
Contents, Vol. 56, 1991 (2004) (0)
Title Page / Table of Contents / Abstracts (1991) (0)
Expression and association of the human trithorax and polycomb group of proteins (2001) (0)
Analysis of circulating protein aggregates reveals pathological hallmarks of amyotrophic lateral sclerosis (2020) (0)
Genetics of Human Neoplasia. Volume 3 of Advances in Genome Biology. Edited by Ram S. Verma. JAI Press, London. 1995. 2 Vols: Pp. 232 & Pp. 248. £125.00 (US$195.00). ISBN: 1 55938 835 8. (1997) (0)
PRODUCTION OF A PANEL OF IRRADIATION-FUSION-GENE TRANSFER HYBRIDS FOR THE MAPPING OF CHROMOSOME-6 LOCI (1991) (0)
Molecular cloning andanalysis ofthefragile X region (1991) (0)
Genetic analysis ofthe15;17 chromosome translocation associated withacutepromyelocytic leukemia (1983) (0)
Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-κB pathways (2015) (0)
The sialomicin CD164, a negative regulator of haemopoiesis, is expressed by CD34 + and erythroid subsets and is located on chromosome 6q21 (1997) (0)
PRECLINICAL EXPERIMENTAL THERAPEUTICS AND PHARMACOLOGY (2010) (0)
Abstracts for the Tenth International Conference on Brain Tumour Research and Therapy (2005) (0)
Correction to: c-MYC overexpression induces choroid plexus papillomas through a T-cell mediated inflammatory mechanism (2019) (0)
Subject Index Vol. 62, 1993 (1993) (0)
LGG-57. SIGNALLING MECHANISMS IN PAEDIATRIC LOW-GRADE GLIOMA (2020) (0)
The 36th American Cytogenetics Conference (2000) (0)
Abstracts from the 2012 BNOS Conference (2012) (0)
Subject Index Vol. 56, 1991 (1991) (0)
Table of Contents (1993) (0)
Large-Scale chromatin structure and function in the Major Histocompatibility Complex (2001) (0)
Structural organization of chromosome 6 in interphase. (1997) (0)
MICRORNA EXPRESSION IN PAEDIATRIC BRAIN TUMOURS (2011) (0)
Juvenile polyposis lesions show clonal loss of SMAD4 in epithelial as well as stromal compartments, endorsing the "gatekeeper" not the "landscaper" hypothesis [Abstract] (2000) (0)
Additional file 1: Table S1. of Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-ÎşB pathways (2015) (0)
Subject Index Vol. 64, 1993 (1993) (0)
PO77EXPRESSION OF THE ONCOGENIC SPLICE VARIANT OF CYCLIN D1, CCND1B, IN PAEDIATRIC LOW GRADE GLIOMAS. (2015) (0)
298 Defective DNA Repair and Chromosomal Instability in RDEB (2019) (0)
LGG-44. Multi-omic analysis reveals integrated signalling networks in paediatric low-grade glioma (2022) (0)
Acute Promyelocytic Leukemia Characterization of Cryptic Rearrangements and Variant Translocations in (2013) (0)
OP17MICRORNA PROFILING USING SMALL RNA-SEQ IN PAEDIATRIC LOW GRADE GLIOMAS (2014) (0)
Isolation ofcDNAclones encoding the isozyme of humanDNAtopoisomerase 11andlocalisation ofthegene tochromosome 3p24 (1992) (0)
Combinatorial generation ofvariable fusion proteins in theEwingfamily oftumours (1993) (0)
LGG Nat Genet Supplemental data 2013 (2013) (0)
Choroid plexus papillomas are induced by c-Myc overexpression in the choroid plexus via a T-cell inflammatory mechanism (2019) (0)
MOLECULAR GENETIC AND EPIGENETIC ANALYSIS OF PEDIATRIC LOW-GRADE ASTROCYTIC GLIOMAS (2008) (0)
Introduction: Genetic rearrangements in cancer (1996) (0)
Probe mapping and tumour breakpoint characterisation on chromosome 11. (1991) (0)
Chromosome-mediated gene thnsfer. (1991) (0)
DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas (2016) (0)
Cytogenetic analysis of paediatric solid tumors (1989) (0)
MICRORNA SIGNATURES IN A BROAD COHORT OF PAEDIATRIC BRAIN TUMOURS (2012) (0)
Spectral Karyotyping reveals a new subset of colorectal cancers characterized by balanced translocations (2001) (0)
PEPTIDE VACCINE THERAPY FOR CHILDHOOD GLIOMAS : INTERIM RESULTS OF A PILOT STUDY (0)

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