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spred1 (39) 39
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Journal Article
Circulation, ISSN 0009-7322, 10/2013, Volume 128, Issue 18, pp. 2026 - 2038
Journal Article
Indian Journal of Medical Research, Supplement, ISSN 0367-9012, 05/2016, Volume 143, Issue Supplement, pp. 91 - 103
Background & objectives: Insidious symptomatology, late clinical presentation and poor prognosis of oesophageal cancer (EC) highlight the pressing need for... 
Oesophageal cancer | SPRED1 | Diagnostic potential | Real-time PCR | Circulating miRNA | PUR-alpha | CIRCULATING MICRORNAS | MEDICINE, RESEARCH & EXPERIMENTAL | PROFILES | HYBRIDIZATION | real-time PCR | IMMUNOLOGY | diagnostic potential | oesophageal cancer | BIOMARKERS | MEDICINE, GENERAL & INTERNAL | NASOPHARYNGEAL CARCINOMA | PATHWAY | COLORECTAL-CANCER | SQUAMOUS-CELL CARCINOMA | EXPRESSION | CLINICAL-SIGNIFICANCE | Prognosis | Membrane Proteins - genetics | Esophageal Neoplasms - blood | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Male | Transcription Factors - biosynthesis | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Intracellular Signaling Peptides and Proteins - biosynthesis | Esophageal Neoplasms - pathology | Biomarkers, Tumor - blood | Membrane Proteins - biosynthesis | Esophageal Neoplasms - genetics | Adult | Female | Aged | Biomarkers, Tumor - genetics | MicroRNAs - blood | MicroRNAs - genetics | DNA-Binding Proteins - biosynthesis | Intracellular Signaling Peptides and Proteins - genetics | MicroRNA | Genetic aspects | Diagnosis | Gene expression | Health aspects | Esophageal cancer | Proteins | Gene amplification | Disease | Medical prognosis | Leukemia | Cell cycle | Real time | Cancer | Tumors | Index Medicus | Original | Circulating miRNA - diagnostic potential - oesophageal cancer - PUR-alpha - real-time PCR - SPRED1
Journal Article
Developmental Cell, ISSN 1534-5807, 08/2008, Volume 15, Issue 2, pp. 272 - 284
Journal Article
Oncogene, ISSN 0950-9232, 01/2015, Volume 34, Issue 5, pp. 631 - 638
Constitutional dominant loss-of-function mutations in the SPRED1 gene cause a rare phenotype referred as neurofibromatosis type 1 (NF1)-like syndrome or Legius... 
childhood leukaemia | neurofibromatosis type 1 | tumour suppressor gene | SPRED1 | café-au-lait spots | Legius syndrome | cafe-au-lait spots | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHENOTYPE | ACUTE MYELOID-LEUKEMIA | CANCER | CELL BIOLOGY | SIGNAL-TRANSDUCTION | ONCOLOGY | ACUTE LYMPHOBLASTIC-LEUKEMIA | GENES | DISEASE | GENETICS & HEREDITY | MUTATIONS | SPECTRUM | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - pathology | Humans | Gene Expression Regulation, Neoplastic | Child, Preschool | Infant | Male | Leukemia, Myeloid, Acute - complications | Cafe-au-Lait Spots - complications | Loss of Heterozygosity - genetics | Female | Child | Genes, Tumor Suppressor | Intracellular Signaling Peptides and Proteins - genetics | Cafe-au-Lait Spots - pathology | Infant, Newborn | Genes, ras - genetics | Cafe-au-Lait Spots - genetics | Leukemia, Myeloid, Acute - pathology | Membrane Proteins - genetics | Intracellular Signaling Peptides and Proteins - biosynthesis | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Membrane Proteins - biosynthesis | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - complications | Adolescent | Mutation | Neurofibromin 1 - genetics | Leukemia, Myeloid, Acute - genetics | Gene mutations | Leukemia in children | Neurofibromatosis | Development and progression | Tumor suppressor genes | Genetic aspects | Research | Health aspects | Risk factors | Studies | Proteins | Genotype & phenotype | Ribonucleic acid--RNA | Leukemia | Tumors | Index Medicus
Journal Article
Journal Article
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 12/2008, Volume 28, Issue 53, pp. 14443 - 14449
Journal Article
JAMA: The Journal of the American Medical Association, ISSN 0098-7484, 11/2009, Volume 302, Issue 19, pp. 2111 - 2118
Journal Article
Leukemia, ISSN 0887-6924, 02/2014, Volume 28, Issue 2, pp. 302 - 310
Journal Article
Journal Article
JAAD Case Reports, ISSN 2352-5126, 05/2018, Volume 4, Issue 4, pp. 390 - 391
Journal Article