Anne M. Bowcock researcher
Bowcock, Anne M.
Bowcock, A. M.
VIAF ID: 14954028 (Personal)
Permalink: http://viaf.org/viaf/14954028
Preferred Forms
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100 0 _ ‡a Anne M. Bowcock ‡c researcher
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200 _ | ‡a Bowcock ‡b Anne M.
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100 1 _ ‡a Bowcock, A. M.
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100 1 _ ‡a Bowcock, Anne M.
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100 1 _ ‡a Bowcock, Anne M.
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100 1 _ ‡a Bowcock, Anne M.
4xx's: Alternate Name Forms (5)
Works
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Breast cancer : molecular genetics, pathogenesis, and therapeutics |
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Functional genomics characterization of genetic predisposing factors in uveal melanoma |
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Génomique fonctionnelle des prédispositions génétiques du mélanome uvéal. |
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High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q. |
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Histone deacetylase inhibitors induce growth arrest and differentiation in uveal melanoma |
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The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14 |
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The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. |
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Human population expansion and microsatellite variation |
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Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. |
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The immunogenetics of Psoriasis: A comprehensive review |
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In vitro transformation of cell lines from human salivary gland tumors |
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Influence of Crohn's disease risk alleles and smoking on disease location |
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Infrequency of BRCA2 alterations in head and neck squamous cell carcinoma. |
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Inhibitory KIR3DL1 alleles are associated with psoriasis. |
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Insights into psoriasis and other inflammatory diseases from large-scale gene expression studies |
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Integrative Copy Number Analysis of Uveal Melanoma Reveals Novel Candidate Genes Involved in Tumorigenesis Including a Tumor Suppressor Role for PHF10/BAF45a |
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Interferon alpha-inducible protein 27 (IFI27) is upregulated in psoriatic skin and certain epithelial cancers. |
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Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitis |
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Investigation of the possible role of WNT genes in human breast cancer. |
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Invited review DNA copy number changes as diagnostic tools for lung cancer |
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JAK3 maps to human chromosome 19p12 within a cluster of proto-oncogenes and transcription factors |
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Linkage analysis of the monoamine A and B genes using newly-defined polymorphisms |
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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. |
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Localization of a gene for familial recurrent arthritis |
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Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR |
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Localization of susceptibility to familial idiopathic scoliosis |
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Localization of the human c-mos gene by in situ hybridization in two cases of acute nonlymphocytic leukemia type M2 |
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Loss of heterozygosity for chromosome 22 DNA sequences in human meningioma |
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Loss of heterozygosity of chromosome 3 detected with single nucleotide polymorphisms is superior to monosomy 3 for predicting metastasis in uveal melanoma |
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Management of resectable colorectal lung metastases |
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Markers and methods for reconstructing modern human history. |
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Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. |
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Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases |
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Microsatellite polymorphism linkage map of human chromosome 13q. |
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Molecular cloning of BRCA1: a gene for early onset familial breast and ovarian cancer |
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The Molecular Revolution in Cutaneous Biology: The Era of Genome-Wide Association Studies and Statistical, Big Data, and Computational Topics |
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Montagna Symposium 2008: The Biologic Basis of Psoriasis |
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Multiple Loci within the major histocompatibility complex confer risk of psoriasis |
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Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene |
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Mutational and haplotype analyses of families with familial partial lipodystrophy |
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A new human RFLP identified by 7D2 places D13S10 proximal to esterase D |
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New insights into the pathogenesis and genetics of psoriatic arthritis |
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Nonlesional atopic dermatitis skin is characterized by broad terminal differentiation defects and variable immune abnormalities |
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Nonrandom distribution of N-myc oncogene genotypes in neuroblastoma |
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Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility. |
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Novel mechanisms of T-cell and dendritic cell activation revealed by profiling of psoriasis on the 63,100-element oligonucleotide array |
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Oncogenic mutations in GNAQ occur early in uveal melanoma |
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Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies |
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The PLC/PRF/5 human hepatoma cell line. II. Chromosomal assignment of hepatitis B virus integration sites |
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Polymorphism and mapping of the IGF1 gene, and absence of association with stature among African Pygmies |
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Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22. |
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Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities |
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Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility |
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Psoriasis bench to bedside: genetics meets immunology |
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Psoriasis: genetic associations and immune system changes. |
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Psoriasis genetics: breaking the barrier |
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Psoriasis mutations disrupt CARD14 autoinhibition promoting BCL10-MALT1-dependent NF-κB activation. |
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Psoriasis pathophysiology: current concepts of pathogenesis |
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Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease |
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Psoriasis vulgaris: cutaneous lymphoid tissue supports T-cell activation and "Type 1" inflammatory gene expression |
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PSORS2 is due to mutations in CARD14. |
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Punctuated evolution of canonical genomic aberrations in uveal melanoma. |
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A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis |
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Rapid detection and sequencing of alleles in the 3' flanking region of the interleukin-6 gene |
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Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis |
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Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma. |
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A regulatory role for 1-acylglycerol-3-phosphate-O-acyltransferase 2 in adipocyte differentiation |
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Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms |
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Report of the First International Workshop on Human Chromosome 13 Mapping. Dallas, Texas, September 21-22, 1992. |
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Reproducible Novel Transcriptional Differences Between Psoriatic Lesional and Non-Lesional Skin Show Increased Inflammation and Metabolism. |
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Reversal of atopic dermatitis with narrow-band UVB phototherapy and biomarkers for therapeutic response |
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RFLPs associated with MDR2, a member of the human multidrug resistance gene family mapped to chromosome 7. |
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Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety. |
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Runx transcription factors repress human and murine c-Myc expression in a DNA-binding and C-terminally dependent manner |
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The single copy probe pG24E2.4 [D13S21] reveals a Bsp1286 RFLP at 13q14.1-q14.2. |
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SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis. |
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An SspI RFLP at the D13S25 locus identified by the anonymous single copy probe H2-42. |
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Structure and characterization of the human tissue inhibitor of metalloproteinases-2 gene |
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The study of variation in the human genome |
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A subset of methylated CpG sites differentiate psoriatic from normal skin. |
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Targeting Skin: Vitiligo and Autoimmunity |
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A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents. |
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Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation |
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Zeroing in on tolerance |
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