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1991, Johns Hopkins series in contemporary medicine and public health., ISBN 9780801841699, xiv, 378
Book
2011, 1. Aufl., ISBN 1405196262, xxi, 416 p., [4] p. of col. plates
This comprehensive book captures and compiles new and current information on hematologic malignancies. New knowledge of cellular disease processes, molecular... 
Leukemia | Lymphomas | Myelodysplastic syndromes
Book
Journal Article
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 06/2014, Volume 166, Issue 2, pp. 140 - 155
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 2006, Volume 117, Issue 4, pp. 725 - 738
The Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder with variable clinical phenotypes that correlate with the type of mutations in the ( ) gene.... 
Wiskott-Aldrich syndrome | X-linked thrombocytopenia | function of WASP | X-linked neutropenia | immune defects | mutation analysis | genotype-phenotype correlation | mutational hotspots | hematopoietic stem cell transplantation | gene therapy | scoring system | ACTIN POLYMERIZATION | IN-VIVO REVERSION | SYNDROME PROTEIN WASP | MEDIATED GENE-TRANSFER | ARP2/3 COMPLEX | T-CELL | IMMUNOLOGY | NK CELL CYTOTOXICITY | HEMATOPOIETIC-CELLS | ALLERGY | EPIDERMAL-GROWTH-FACTOR | Wiskott-Aldrich Syndrome Protein - genetics | Wiskott-Aldrich Syndrome - immunology | Neoplasms - etiology | Signal Transduction | Thrombocytopenia - etiology | Humans | Actins - metabolism | Cell Communication | Genotype | Male | Autoimmune Diseases - etiology | Wiskott-Aldrich Syndrome - genetics | Eczema - etiology | Thrombocytopenia - blood | Wiskott-Aldrich Syndrome - physiopathology | Phenotype | Models, Biological | Wiskott-Aldrich Syndrome Protein - metabolism | Mutation | Wiskott-Aldrich Syndrome - complications | Cell Movement | Medical colleges | Immunoglobulins | Genetic disorders | Dendritic cells | Children's hospitals | Guanosine | Polymerization | Transplantation | Muscle proteins | Hematopoietic stem cells | Phosphatidylinositol | Actin | Analysis | Children | Health aspects | Motility | Ear diseases | Gene expression | Patients | Cell adhesion & migration | Defects | Proteins | Genotype & phenotype | Genetic counseling | Lymphocytes | Eczema | Binding sites | Immune system
Journal Article
Human Mutation, ISSN 1059-7794, 09/2016, Volume 37, Issue 9, pp. 847 - 864
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 5/2013, Volume 70, Issue 9, pp. 1543 - 1573
Epigenetic mechanisms play an important role in gene regulation during development. DNA methylation, which is probably the most important and best-studied... 
Life Sciences | Biochemistry, general | Life Sciences, general | Disease | Epigenetics | Mutation | Biomedicine general | Cell Biology | SYSTEMIC-LUPUS-ERYTHEMATOSUS | RUBINSTEIN-TAYBI-SYNDROME | BIOCHEMISTRY & MOLECULAR BIOLOGY | S-ADENOSYLMETHIONINE SYNTHETASE | CPG-BINDING-PROTEIN | XNP/ATR-X GENE | METHIONINE ADENOSYLTRANSFERASE 1A | CELL BIOLOGY | FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY | COFFIN-LOWRY-SYNDROME | SINGLE NUCLEOTIDE POLYMORPHISM | GLYCINE N-METHYLTRANSFERASE | Coffin-Lowry Syndrome - genetics | Neoplasms - metabolism | Epigenesis, Genetic | Humans | Lupus Erythematosus, Systemic - metabolism | Muscular Dystrophy, Facioscapulohumeral - genetics | alpha-Thalassemia - metabolism | DNA Methylation | Mental Retardation, X-Linked - genetics | Rubinstein-Taybi Syndrome - genetics | Neoplasms - genetics | Sotos Syndrome - metabolism | Coffin-Lowry Syndrome - metabolism | alpha-Thalassemia - genetics | Muscular Dystrophy, Facioscapulohumeral - metabolism | Sotos Syndrome - genetics | DNA Modification Methylases - metabolism | Cockayne Syndrome - metabolism | DNA - metabolism | Rubinstein-Taybi Syndrome - metabolism | DNA - genetics | Rett Syndrome - metabolism | DNA Modification Methylases - genetics | Animals | Histones - genetics | CHARGE Syndrome - metabolism | Lupus Erythematosus, Systemic - genetics | Cockayne Syndrome - genetics | CHARGE Syndrome - genetics | Histones - metabolism | Rett Syndrome - genetics | Mental Retardation, X-Linked - metabolism | Liver cancer | Gene mutations | Genes | Transferases | Immunodeficiency | Physiological aspects | Methylation | Glycine | Mental illness | S-adenosylmethionine | CHARGE syndrome
Journal Article