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2009, Shohan., ISBN 9784886114259, 4 v.
Book
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 6, pp. 1914 - 1922
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 140, Issue 1, pp. 223 - 231
Background Ikaros, which is encoded by IKZF1 , is a transcriptional factor that play a critical role in hematopoiesis. Somatic IKZF1 alterations are known to... 
Allergy and Immunology | Acute lymphoblastic leukemia | Ikaros | common lymphoid progenitor | dysgammaglobulinemia | nuclear localization | B-cell deficiency | IKZF1 | autoimmune disease | germline mutation | DNA binding | SYSTEM | ZINC FINGERS | ACTIVATION | DEFECTS | STAGE | B-CELL DIFFERENTIATION | IMMUNOLOGY | ALLERGY | LEUKEMOGENESIS | LYMPHOBLASTIC-LEUKEMIA | Autoimmunity | Humans | Autoimmune Diseases - immunology | Hematopoiesis - genetics | Male | Hematologic Diseases - immunology | Autoimmune Diseases - genetics | Ikaros Transcription Factor - genetics | Young Adult | B-Lymphocytes - immunology | Ikaros Transcription Factor - immunology | Adolescent | Germ-Line Mutation | Hematologic Diseases - genetics | Lymphocyte Count | Adult | Female | T-Lymphocytes - immunology | Child | Medical colleges | Developmental biology | Analysis | Leukemia | Immunodeficiency | Genetic aspects | Pediatrics | Flow cytometry | Lymphopoiesis | Transcription factors | Ikaros protein | Pathogenesis | Genomes | Kinases | Immunoglobulin A | Vasculitis | Systemic lupus erythematosus | Hematopoiesis | Cell cycle | Bone marrow | Localization | Age | Deoxyribonucleic acid--DNA | Binding | Nucleotide sequence | Abnormalities | Patients | Hemopoiesis | Diseases | Thrombocytopenic purpura | Chronic conditions | Lymphocytes B | Plasmids | Purpura | Pancytopenia | Stem cells | Mutation | Autoimmune diseases | Position (location) | Index Medicus | Abridged Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 03/2018, Volume 378, Issue 11, pp. 995 - 1003
Journal Article
by Aung, T and Ozaki, M and Lee, M.C and Schlotzer-Schrehardt, U and Thorleifsson, G and Mizoguchi, T and Igo, R.P., Jr and Haripriya, A and Williams, S.E and Astakhov, Y.S and Orr, A.C and Burdon, K.P and Nakano, S and Mori, K and Abu-Amero, K and Hauser, M and Li, Z and Prakadeeswari, G and Bailey, J.N and Cherecheanu, A.P and Kang, J.H and Nelson, S and Hayashi, K and Manabe, S.I and Kazama, S and Zarnowski, T and Inoue, K and Irkec, M and Coca-Prados, M and Sugiyama, K and Jarvela, I and Schlottmann, P and Lerner, S.F and Lamari, H and Nilgun, Y and Bikbov, M and Park, K.H and Cha, S.C and Yamashiro, K and Zenteno, J.C and Jonas, J.B and Kumar, R.S.S and Perera, S.A and Chan, A.S.Y and Kobakhidze, N and George, R and Vijaya, L and Do, T and Edward, D.P and Juan Marcos, L. de and Pakravan, M and Moghimi, S and Ideta, R and Bach-Holm, D and Kappelgaard, P and Wirostko, B and Thomas, S and Gaston, D and Bedard, K and Greer, W.L and Yang, Z and Chen, X and Huang, L and Sang, J and Jia, H and Jia, L and Qiao, C and Zhang, H and Liu, X and Zhao, B and Wang, Y.X and Xu, L and Leruez, S and Reynier, P and Chichua, G and Tabagari, S and Uebe, S and Zenkel, M and Berner, D and Mossbock, G and Weisschuh, N and Hoja, U and Welge-Luessen, U.C and Mardin, C and Founti, P and Chatzikyriakidou, A and Pappas, T and Anastasopoulos, E and Lambropoulos, A and Ghosh, A and Shetty, R and Porporato, N and Saravanan, V and Venkatesh, R and Shivkumar, C and Kalpana, N and Sarangapani, S and Kanavi, M.R and Beni, A.N and Yazdani, S and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 7, pp. 993 - 1004
Exfoliation syndrome (XFS) is the most common known risk factor for secondary glaucoma and a major cause of blindness worldwide. Variants in two genes, LOXL1... 
INDIVIDUALS | RISK LOCI | PSEUDOEXFOLIATION SYNDROME | INFLAMMATORY-BOWEL-DISEASE | METAANALYSIS | POLYMORPHISMS | COMMON SEQUENCE VARIANTS | GENETICS & HEREDITY | GLAUCOMA | BLOOD-PRESSURE | GENOME-WIDE ASSOCIATION | Haplotypes | Humans | Asian Continental Ancestry Group - genetics | Extracellular Matrix - metabolism | Male | Gene Expression Profiling | Mutation, Missense | Amino Acid Oxidoreductases - genetics | Exfoliation Syndrome - ethnology | RNA, Messenger - biosynthesis | Aged, 80 and over | Female | Spheroids, Cellular | Calcium Channels - genetics | Molecular Chaperones - biosynthesis | Eye - metabolism | Genetic Predisposition to Disease | Genome-Wide Association Study | Amino Acid Oxidoreductases - physiology | Molecular Chaperones - genetics | Cell Adhesion | Point Mutation | Alleles | Exfoliation Syndrome - genetics | Amino Acid Substitution | Exfoliatins | Disease susceptibility | Genetic aspects | Analysis | Risk factors | Glaucoma | Genes | Principal components analysis | Cardiovascular disease | Genomes | Biology | Loci | Exfoliation | Studies | Collaboration | Blindness | Alzheimers disease | Index Medicus | Life Sciences | Populations and Evolution | Microbiology and Parasitology | Parasitology | Quantitative Methods | Computer Science | Genetics | Santé publique et épidémiologie | Bioinformatics | Human genetics | Virology
Journal Article
Journal of Pharmacological Sciences, ISSN 1347-8613, 04/2018, Volume 136, Issue 4, pp. 212 - 217
The natural compound, curcumin (CUR), possesses several pharmacological properties, including p300-specific histone acetyltransferase (HAT) inhibitory... 
p300 | Demethoxycurcumin | Curcumin | Cardiomyocyte hypertrophy | Bisdemethoxycurcumin | Turmeric | Histones | Physiological aspects | Chemical properties | Hypertrophy | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 05/2016, Volume 6, Issue 1, pp. 26113 - 26113
The corneal endothelium maintains corneal transparency; consequently, its dysfunction causes severe vision loss. Tissue engineering-based therapy, as an... 
GRAFT-REJECTION | SURVIVAL | KERATOPLASTY | MONKEY | IN-VITRO | MEMBRANE | MULTIDISCIPLINARY SCIENCES | RISK | SHEET | PROLIFERATIVE CAPACITY | TRANSPLANTATION | Cornea | Transplants & implants | Actomyosin | Tissue engineering | Good Manufacturing Practice | Anterior chamber | Transplantation | Contraction | Endothelial cells | Rho-associated kinase | Endothelium | Index Medicus
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 02/2018, Volume 65, Issue 2, pp. e26831 - n/a
Autoimmune diseases in children are rare and can be difficult to diagnose.  Single causative genes have been identified for some pediatric autoimmune diseases.... 
autoimmune lymphoproliferative syndrome | lymphoproliferation | autoimmunity | whole exome sequencing analysis | LOSS-OF-FUNCTION | ONCOLOGY | STAT3 | GERMLINE MUTATIONS | PEDIATRICS | HEMATOLOGY | Autoimmunity | Children | Autoimmune diseases | Diseases | CTLA-4 protein | Lymphocytes | Genes | Stat3 protein | Diagnostic systems | Patients | Gene sequencing | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2014, Volume 9, Issue 12, pp. e112291 - e112291
Neural crest cells (NCCs) are an embryonic migratory cell population with the ability to differentiate into a wide variety of cell types that contribute to the... 
MAINTENANCE | BRANCHIAL ARCHES | MULTIDISCIPLINARY SCIENCES | MOUSE | PATIENT-SPECIFIC IPSCS | GENERATION | DIFFERENTIATION | INDUCTION | SPECIFICATION | PARAXIAL MESODERM | MELANOCYTES | Chondrocytes - cytology | Neural Crest - cytology | Cell Proliferation | Embryonic Stem Cells - cytology | Pluripotent Stem Cells - cytology | Oligonucleotide Array Sequence Analysis | Cells, Cultured - cytology | Humans | Cell Lineage | Cornea - metabolism | Bone Morphogenetic Proteins - metabolism | Insulin - metabolism | Mesenchymal Stromal Cells - cytology | Flow Cytometry | Endothelial Cells - cytology | Melanocytes - cytology | Cell Differentiation | Culture Media - chemistry | Induced Pluripotent Stem Cells - cytology | DNA, Complementary - metabolism | Transforming Growth Factor beta - metabolism | Osteogenesis | Fibroblasts - metabolism | Fibroblast growth factors | Skin | Transforming growth factors | Gene expression | Embryonic stem cells | Biopharmaceutics | Cell culture | Pediatrics | Cornea | Media (culture) | Mesenchyme | Embryo cells | Melanocytes | Nervous system | Neuronal-glial interactions | Cell growth | Epidermal growth factor | Surgery | Growth factors | Biomedical engineering | Fibroblast growth factor 2 | Peripheral nervous system | Tissue engineering | Insulin | Neural crest | Embryos | Pigmentation | Endothelial cells | Medicine | Organic chemistry | Inhibitors | Animal behavior | Stromal cells | Stem cells | Differentiation | Pluripotency | Cell migration | Inhibitory postsynaptic potentials | Index Medicus
Journal Article