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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2012, Volume 109, Issue 22, pp. 8646 - 8651
A genome-wide association study of papillary thyroid carcinoma (PTC) pinpointed two independent SNPs (rs944289 and rs965513) located in regions containing no... 
COS cells | Thyroid cancer | Papillary carcinoma | RNA | Complementary DNA | Exons | Genes | Cell lines | Alleles | Tumors | Transcriptional regulation | Germline variant | Tissue specific expression | COMMON VARIANTS | POPULATION | transcriptional regulation | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | LOCI | germline variant | CCAAT/ENHANCER-BINDING-PROTEIN | C/EBP-ALPHA | tissue specific expression | CANCER-RISK | TRANSCRIPTION FACTOR | EXPRESSION | GENOME-WIDE ASSOCIATION | Carcinoma, Papillary - genetics | Cell Proliferation | Oligonucleotide Array Sequence Analysis | Humans | Gene Expression Regulation, Neoplastic | Cercopithecus aethiops | Molecular Sequence Data | Gene Expression Profiling | RNA, Untranslated - genetics | HEK293 Cells | Genes, Tumor Suppressor | Genetic Predisposition to Disease - genetics | Genotype | Binding Sites - genetics | Reverse Transcriptase Polymerase Chain Reaction | Carcinoma, Papillary - pathology | CCAAT-Enhancer-Binding Protein-beta - metabolism | Thyroid Neoplasms - genetics | Blotting, Northern | Animals | Cell Line, Tumor | Polymorphism, Single Nucleotide | COS Cells | Chromosomes, Human, Pair 14 - genetics | Thyroid Neoplasms - pathology | Carcinoma | Physiological aspects | Development and progression | Tumor suppressor genes | Genetic aspects | Research | Health aspects | Genetic polymorphisms | Cancer | Genomes | Ribonucleic acid--RNA | Gene expression | Binding sites | Polymorphism | Index Medicus | Biological Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2005, Volume 102, Issue 52, pp. 19075 - 19080
Journal Article
Science, ISSN 0036-8075, 4/2011, Volume 332, Issue 6026, pp. 238 - 240
Journal Article
International Journal of Cancer, ISSN 0020-7136, 02/2019, Volume 144, Issue 3, pp. 503 - 512
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2015, Volume 112, Issue 19, pp. 6128 - 6133
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2007, Volume 104, Issue 8, pp. 2803 - 2808
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 04/2018, Volume 103, Issue 4, pp. 1369 - 1379
Context: Previous genome-wide association studies have shown that single-nucleotide polymorphism (SNP) rs2439302 in chromosome 8p12 is significantly associated... 
COMMON VARIANTS | POPULATION | CANCER RISK | SUSCEPTIBILITY | DISEASE | ENDOCRINOLOGY & METABOLISM | LOCI | ENHANCERS | EXPRESSION | HEREGULIN | GENOME-WIDE ASSOCIATION | Haplotypes | RNA, Small Interfering - genetics | Carcinoma, Papillary - genetics | Humans | Middle Aged | Male | Neuregulin-1 - biosynthesis | Carcinoma, Papillary - metabolism | Neuregulin-1 - genetics | Gene Knockdown Techniques | Adult | Female | Transcription, Genetic | Neoplasm Proteins - genetics | Gene Expression Regulation, Neoplastic - physiology | Genetic Predisposition to Disease | Neoplasm Proteins - biosynthesis | Genotype | Thyroid Cancer, Papillary | Thyroid Neoplasms - genetics | Protein Isoforms - biosynthesis | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Thyroid Gland - metabolism | Protein Isoforms - genetics | Thyroid Neoplasms - metabolism | Chromatin | Immunoprecipitation | Genes | Gene regulation | Reverse transcription | Risk | Genomes | Single-nucleotide polymorphism | Assaying | Gene polymorphism | Gene sequencing | Thyroid carcinoma | Genotypes | Deoxyribonucleic acid--DNA | Thyroid | Health risks | siRNA | Gene expression | Polymerase chain reaction | Thyroid cancer | Ribonucleic acids | Isoforms | Alleles | Chromosome 8 | Papillary thyroid carcinoma | Cancer | Polymorphism | Index Medicus | Abridged Index Medicus
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 56 - 56
Background: Inherited malabsorption of cobalamin (Cbl) causes hematological and neurological abnormalities that can be fatal. Three genes have been implicated... 
Cobalamin | Founder mutation | Gastric intrinsic factor | Cubilin | Vitamin B | Ancestry | Genetic testing | Amnionless | Genetic heterogeneity | Hereditary cobalamin malabsorption | MEDICINE, RESEARCH & EXPERIMENTAL | VITAMIN B-12 RECEPTOR | INTRINSIC-FACTOR GENE | CELLULAR UPTAKE | Vitamin B-12 | VISCERAL-ENDODERM | SELECTIVE INTESTINAL MALABSORPTION | GENETICS & HEREDITY | TRANSCOBALAMIN-I HAPTOCORRIN | IMERSLUND-GRASBECK-SYNDROME | MOUSE GASTRULATION | Vitamin B 12 Deficiency - ethnology | Genetic Testing | Genetic Association Studies | Malabsorption Syndromes - ethnology | Humans | Male | Proteinuria - genetics | Genetic Heterogeneity | Intrinsic Factor - genetics | Malabsorption Syndromes - genetics | Proteins - genetics | Founder Effect | Ethnic Groups - genetics | Proteinuria - ethnology | Anemia, Megaloblastic | Vitamin B 12 Deficiency - genetics | Female | Mutation | Vitamin B 12 - metabolism | Intrinsic Factor - metabolism | Gene mutations | Malabsorption syndromes | Physiological aspects | Genetic aspects | Research | Vitamin B12 | Health aspects | Risk factors | RNA sequencing | Medical research | Nervous system diseases | RNA | Genes | Genetic research | Medicine, Experimental | Genetic screening | Genetic polymorphisms | Studies | Genetic counseling | Genetics | Homocysteine | Manuscripts | Cancer | Index Medicus
Journal Article
Nature Communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, pp. 14517 - 14517
Journal Article