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Wilson, Robert
One or more keywords matched the following properties of Wilson, Robert
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phone 843-876-2217
One or more keywords matched the following items that are connected to Wilson, Robert
Item TypeName
Academic Article Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations.
Academic Article Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.
Academic Article Resistance to multiple steroids in two sisters.
Academic Article Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment.
Academic Article Hypertension and adrenal disorders.
Academic Article Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency).
Academic Article Apparent mineralocorticoid excess.
Academic Article Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies.
Academic Article Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency.
Academic Article Nonclassic 21-hydroxylase deficiency in Croatia.
Academic Article In vitro expression studies of a novel mutation delta299 in a patient affected with apparent mineralocorticoid excess.
Academic Article Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
Academic Article The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase gene.
Academic Article Monogenic low renin hypertension.
Academic Article Two novel mutations found in a patient with 17alpha-hydroxylase enzyme deficiency.
Academic Article Aldosterone-to-renin ratio as a marker for disease severity in 21-hydroxylase deficiency congenital adrenal hyperplasia.
Academic Article Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency.
Academic Article Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17?HSD-3 defect confirmed by molecular analysis.
Academic Article CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish children.
Concept Karyotyping
Concept Dexamethasone
Concept DNA Methylation
Concept Oman
Concept Breast
Concept Software
Concept Incidence
Concept Prostatic Neoplasms
Concept Introns
Concept Steroid 21-Hydroxylase
Concept Proto-Oncogene Protein c-fli-1
Concept PTEN Phosphohydrolase
Concept Oncogenes
Concept Gene Expression
Concept Cyclin-Dependent Kinases
Concept Endangered Species
Concept Phenylenediamines
Concept RNA Interference
Concept RNA Editing
Concept Steroid 17-alpha-Hydroxylase
Concept Cortisone
Concept Amyotrophic Lateral Sclerosis
Concept DNA Fragmentation
Concept Turkey
Concept Cricetinae
Concept Genetic Testing
Concept Molecular Biology
Concept Syndrome
Concept Computer Simulation
Concept STAT5 Transcription Factor
Concept Amino Acid Sequence
Concept Algorithms
Concept Cohort Studies
Concept Antineoplastic Agents
Concept Cytochrome P-450 Enzyme System
Concept DNA, Intergenic
Concept Adrenal Hyperplasia, Congenital
Concept Mesencephalon
Concept STAT3 Transcription Factor
Concept CHO Cells
Concept Rivers
Concept Tumor Stem Cell Assay
Concept Cricetulus
Concept Hydrocortisone
Concept Genetic Predisposition to Disease
Concept Diencephalon
Concept Tumor Cells, Cultured
Concept Protein Tyrosine Phosphatase, Non-Receptor Type 11
Concept Dietary Supplements
Concept Chromatin
Concept Sodium
Concept Chromosomes, Human, Pair 6
Concept DNA Primers
Concept Adenocarcinoma
Concept Renin
Concept Estrogens
Concept Exons
Concept Codon
Concept Retrospective Studies
Concept Phospholipase C gamma
Concept Computational Biology
Concept Neonatal Screening
Concept Genes, Neoplasm
Concept Academic Medical Centers
Concept Monocytes
Concept Cell Proliferation
Concept CpG Islands
Concept Drug Screening Assays, Antitumor
Concept Adrenal Medulla
Concept Aneuploidy
Concept Croatia
Concept Carcinoma, Non-Small-Cell Lung
Concept Ambulatory Care Facilities
Concept Microsatellite Repeats
Concept Gestational Age
Concept Cluster Analysis
Concept ras Proteins
Concept 17-alpha-Hydroxyprogesterone
Concept Genetic Carrier Screening
Concept Fundulidae
Concept Spheroids, Cellular
Concept Chorionic Villi Sampling
Concept Chromosomes, Human, Pair 8
Concept Clinical Laboratory Techniques
Concept Hypothalamo-Hypophyseal System
Concept Prospective Studies
Concept 3' Untranslated Regions
Concept Fetal Growth Retardation
Concept Cross-Sectional Studies
Concept Amniocentesis
Concept Steroid 11-beta-Hydroxylase
Concept Histocompatibility Testing
Concept Fresh Water
Concept Cell Line
Concept Cholecalciferol
Concept Promoter Regions, Genetic
Concept Steroids
Concept Base Sequence
Concept Alleles
Concept Genes, Recessive
Concept Follow-Up Studies
Concept Aldosterone
Concept Siblings
Concept Proto-Oncogene Proteins c-ets
Concept Cell Line, Tumor
Concept Age Distribution
Academic Article KAT6A, a chromatin modifier from the 8p11-p12 amplicon is a candidate oncogene in luminal breast cancer.
Academic Article FLI1 expression is correlated with breast cancer cellular growth, migration, and invasion and altered gene expression.
Academic Article Oncogenic signaling in amphiregulin and EGFR-expressing PTEN-null human breast cancer.
Academic Article Functional oncogene signatures guide rationally designed combination therapies to synergistically induce breast cancer cell death.
Academic Article Amplification of WHSC1L1 regulates expression and estrogen-independent activation of ERa in SUM-44 breast cancer cells and is associated with ERa over-expression in breast cancer.
Academic Article Multivariate models from RNA-Seq SNVs yield candidate molecular targets for biomarker discovery: SNV-DA.
Academic Article Systems analysis of the prostate transcriptome in African-American men compared with European-American men.
Academic Article Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.
Academic Article A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.
Academic Article Complementary feature selection from alternative splicing events and gene expression for phenotype prediction.
Academic Article Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11?-hydroxysteroid dehydrogenase type 2 deficiency.
Academic Article A Novel CLCN5 Mutation Associated With?Focal Segmental Glomerulosclerosis and?Podocyte Injury.
Academic Article ErbB4 promotes malignant peripheral nerve sheath tumor pathogenesis via Ras-independent mechanisms.
Academic Article The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus).
Academic Article Differential DNA Methylation Landscape in Skin Fibroblasts from African Americans with Systemic Sclerosis.
Academic Article Establishment and genomic characterization of a sporadic malignant peripheral nerve sheath tumor cell line.
Academic Article Development and implementation of the SUM breast cancer cell line functional genomics knowledge base.
Academic Article Evidence for Differentiation of Colon Tissue Microbiota in Patients with and without Postoperative Hirschsprung's Associated Enterocolitis: A Pilot Study.
Academic Article Inhibition of the transcriptional kinase CDK7 overcomes therapeutic resistance in HER2-positive breast cancers.
Academic Article Assessing Evolutionary Significant Units (ESU) of the Endangered Freshwater Pearl Mussel (Margaritifera margaritifera) in Southeast Norway on the Basis of Genetic Analysis.
Concept Machine Learning
Concept Transcriptome
Concept Gene Ontology
Concept EGF Family of Proteins
Concept Amphiregulin
Concept HEK293 Cells
Academic Article DNA methylation patterns vary in boar sperm cells with different levels of DNA fragmentation.
Academic Article A Systems Approach to Interrogate Gene Expression Patterns in African American Men Presenting with Clinically Localized Prostate Cancer.
Academic Article Postmortem Diagnosis of the Proteus Syndrome by Next Generation Sequencing of Affected Brain Tissue.
Academic Article Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.
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