Dean, Michael Carlton
مايكل دين
دين، مايكل
Dean, Michael
VIAF ID: 31044046 (Personal)
Permalink: http://viaf.org/viaf/31044046
Preferred Forms
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100 1 _ ‡a Dean, Michael
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100 1 _
‡a
Dean, Michael Carlton
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100 1 _ ‡a Dean, Michael Carlton
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100 1 _
‡a
Dean, Michael Carlton
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100 1 _ ‡a Dean, Michael Carlton
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100 1 _ ‡a دين، مايكل
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100 0 _
‡a
مايكل دين
4xx's: Alternate Name Forms (7)
Works
| Title | Sources |
|---|---|
| The human ATP-binding cassette (ABC) transporter superfamily, 2002: |
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| Identification of the cystic fibrosis gene: chromosome walking and jumping |
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| In Search of AIDS-Resistance Genes |
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| Increased incidence and disparity of diagnosis of retinoblastoma patients in Guatemala |
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| Induction of c-fos and c-myc mRNA by epidermal growth factor or calcium ionophore is cAMP dependent |
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| Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident |
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| Linkage mapping of human polymorphic proteins identified by two-dimensional electrophoresis |
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| LMTK3 confers chemo-resistance in breast cancer. |
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| Long homopurine*homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region |
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| Low-cost HPV testing and the prevalence of cervical infection in asymptomatic populations in Guatemala. |
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| Mapping and sequencing of two yeast genes belonging to the ATP-binding cassette superfamily. |
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| Mapping of 22 Notl linking clones on human chromosome 3 by polymerase chain reaction and somatic cell hybrid panels. |
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| Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16. |
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| Mapping of the serotonin 5-HT1D alpha autoreceptor gene |
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| Mechanism of met oncogene activation |
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| Molecular cloning and characterization of the human ErbB4 gene: identification of novel splice isoforms in the developing and adult brain |
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| Molecular cloning of a brain-specific, developmentally regulated neuregulin 1 (NRG1) isoform and identification of a functional promoter variant associated with schizophrenia |
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| Molecular evolutionary analysis of ABCB5: the ancestral gene is a full transporter with potentially deleterious single nucleotide polymorphisms |
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| Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls |
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| Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients |
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| Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A) |
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| Mutational analysis of ABCG2: role of the GXXXG motif |
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| Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients |
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| Mutational studies of G553 in TM5 of ABCG2: a residue potentially involved in dimerization |
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| Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance |
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| Natural animal models of human genetic diseases |
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| Naturally occurring CCR5 extracellular and transmembrane domain variants affect HIV-1 Co-receptor and ligand binding function |
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| New inhibitors of ABCG2 identified by high-throughput screening |
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| Novel alleles of the chemokine-receptor gene CCR5. |
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| A novel germ line juxtamembrane Met mutation in human gastric cancer |
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| Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease |
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| Novel mutations of the MET proto-oncogene in papillary renal carcinomas. |
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| Organization of the ABCR gene: analysis of promoter and splice junction sequences |
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| A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy |
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| Polarity, proliferation and the hedgehog pathway. |
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| A polymorphic dinucleotide repeat in the third intron of TAP1. |
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| Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3 |
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| Polymorphisms in multidrug resistance 1 (MDR1) gene are associated with refractory Crohn disease and ulcerative colitis |
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| Polymorphisms in the 3' untranslated region of the I kappa B/MAD-3 (NFKBI) gene located on chromosome 14. |
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| Population and pedigree studies reveal a lack of association between the dopamine D2 receptor gene and alcoholism |
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| Population distribution of the functional caspase-12 allele |
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| Preparation of high titer lambda phage lysates |
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| Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts |
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| Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region. |
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| Purification and ATP hydrolysis of the putative cholesterol transporters ABCG5 and ABCG8 |
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| A rare null allele potentially encoding a dominant-negative TRIM5alpha protein in Baka pygmies |
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| The regulation of immunoglobulin genes ... 1984 |
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| Reply to 'Mosaic loss of chromosome Y in leukocytes matters' |
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| Resolving DNA mutations |
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| Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR |
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| Retrospective family study of childhood medulloblastoma. |
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| Risk for HIV-1 infection associated with a common CXCL12 (SDF1) polymorphism and CXCR4 variation in an African population |
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| The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas |
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| Screening for CF mutations in adult cystic fibrosis patients with a directed and optimized SSCP strategy. |
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| Screening for cystic fibrosis mutations in Southern France: Identification of a frameshift mutation and two missense variations |
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| Screening methods for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in non-human primates |
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| Sequence of MET protooncogene cDNA has features characteristic of the tyrosine kinase family of growth-factor receptors |
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| The serum growth and survival requirements of SV40-transformed 3T3 cells |
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| Single-cell exome sequencing reveals single-nucleotide mutation characteristics of a kidney tumor |
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| Single-cell transcriptomics reveals regulators underlying immune cell diversity and immune subtypes associated with prognosis in nasopharyngeal carcinoma |
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| SMUCKLER/TIM4 is a distinct member of TIM family expressed by stromal cells of secondary lymphoid tissues and associated with lymphotoxin signaling |
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| Specific regulation of c-myc oncogene expression in a murine B-cell lymphoma |
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| Statistical estimation and pedigree analysis of CCR2-CCR5 haplotypes |
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| Structural analogues of smoothened intracellular loops as potent inhibitors of Hedgehog pathway and cancer cell growth |
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| Structural and functional diversity calls for a new classification of ABC transporters |
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| Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens. |
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| The suppression of cellular proliferation in SV40-transformed 3T3 cells by glucocorticoids |
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| Surfactant Composition and Function in Patients with ABCA3 Mutations |
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| Targeted therapy for cancer stem cells: the patched pathway and ABC transporters |
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| TET2 binds the androgen receptor and loss is associated with prostate cancer |
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| Towards a unified model of tumor suppression: lessons learned from the human patched gene |
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| Tumor Copy Number Deconvolution Integrating Bulk and Single-Cell Sequencing Data: Supplementary Materials |
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| Tumour stem cells and drug resistance |
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| Typing of HLA-DQA1 and DQB1 using DNA single-strand conformation polymorphism |
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| UBIAD1 mutation alters a mitochondrial prenyltransferase to cause Schnyder corneal dystrophy |
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| Unique features of TRIM5alpha among closely related human TRIM family members |
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| The use of DNA heteroduplex patterns to map recombination within the HLA class II region. |
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| Variants of CCR5, which are permissive for HIV-1 infection, show distinct functional responses to CCL3, CCL4 and CCL5. |
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| Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration |
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| Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people |
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| Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil |
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