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2004, The handbook of experimental animals., ISBN 9780123364258, xvi, 600
Among animals used in research, teaching and testing, mice are now widely recognized as the most important model for human diseases and disorders. They... 
Mice as laboratory animals | Medicine: General Issues
Book
2012, 1. Aufl., Results and problems in cell differentiation, ISBN 9783642304057, Volume 55, viii, 738
The mouse is a perfect model organism to study mammalian, and thus indirectly also human, embryology. Most scientific achievements that have had an important... 
Gene Function | Developmental biology | Cytology | Stem cells | Development | Mice | Life sciences | Cell Biology | Medicine: General Issues | Physiology
Book
1992, ISBN 0124020356, xvi, 512
Book
2016, annotated edition, ISBN 0128000430, x, 331 pages
Kaufman's Atlas of Mouse Development: With Coronal Sections continues the stellar reputation of the original Atlas by providing updated, in-depth anatomical... 
Mice | Histology | Anatomy | Embryos | Biology, life sciences
Book
2012, Results and problems in cell differentiation, ISBN 9783642304057, Volume 55
Web Resource
2015, ISBN 1420070088, xvi, 430
Pathology of the Developing Mouse provides, in so far as feasible, one complete reference on the design, analysis, and interpretation of abnormal findings that... 
Development | Mice | Diseases | Biology, life sciences | Laboratory Animal Science | Developmental Biology | Neuroscience
Book
Journal of Clinical Investigation, ISSN 0021-9738, 03/2009, Volume 119, Issue 3, pp. 565 - 572
Th17 cells are involved in. the pathogenesis of many autoimmune diseases, but it is not clear whether they play a pathogenic role in type I diabetes. Here we... 
ENCEPHALOMYELITIS | MEDICINE, RESEARCH & EXPERIMENTAL | INTERFERON-GAMMA RECEPTOR | NOD MICE | TGF-BETA | NONOBESE DIABETIC MICE | IN-VIVO | DIFFERENTIATION | T-HELPER TYPE-1 | EXPRESSION | CUTTING EDGE | Gene Expression - drug effects | Xenopus Proteins - genetics | Pancreas - cytology | Interleukin-17 - immunology | Th17 Cells - transplantation | Adoptive Transfer | Interferon-gamma - metabolism | Th1 Cells - immunology | Th1 Cells - transplantation | Th1 Cells - metabolism | Th17 Cells - drug effects | Th17 Cells - metabolism | Gene Expression - immunology | Receptors, Interleukin-12 - genetics | Th17 Cells - cytology | Diabetes Mellitus, Type 1 - immunology | Interferon-gamma - genetics | Macrophages - immunology | Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics | Interleukin-12 - pharmacology | Basic Helix-Loop-Helix Transcription Factors - genetics | Antibodies, Monoclonal - pharmacology | Mice, Inbred C57BL | Receptors, Aryl Hydrocarbon - genetics | Interleukin-17 - genetics | Up-Regulation - genetics | Lymph Nodes - immunology | Lymph Nodes - cytology | Mice, SCID | Pancreas - immunology | Receptors, Interleukin - genetics | T-Box Domain Proteins - genetics | Down-Regulation - genetics | Cell Differentiation - immunology | Interleukin-17 - metabolism | Macrophages - metabolism | Animals | Cell Differentiation - drug effects | Diabetes Mellitus, Type 1 - blood | Interferon-gamma - immunology | Th17 Cells - immunology | Macrophages - drug effects | Mice, Inbred NOD | Mice | Th1 Cells - cytology | Blood Glucose - metabolism | Causes of | Physiological aspects | Development and progression | Research | Diabetes | Autoimmune diseases | T cells
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2009, Volume 5, Issue 9, p. e1000650
Cornelia de Lange Syndrome (CdLS) is a multi-organ system birth defects disorder linked, in at least half of cases, to heterozygous mutations in the NIPBL... 
SISTER-CHROMATID COHESION | CONTROL REGION | ENHANCER-BLOCKING ACTIVITY | NIPPED-B | CONGENITAL HEART-DISEASE | GENETICS & HEREDITY | GENE-EXPRESSION | ADIPOCYTE DIFFERENTIATION | OPHTHALMOLOGIC FINDINGS | BRACHMANN-DELANGE SYNDROME | MICE LACKING | Bone and Bones - pathology | Cadherins - metabolism | Craniofacial Abnormalities - physiopathology | Heart Defects, Congenital - genetics | Organ Specificity - genetics | Nervous System Malformations - physiopathology | Sister Chromatid Exchange | Craniofacial Abnormalities - pathology | Transcription, Genetic | Cadherins - genetics | Nervous System Malformations - genetics | Craniofacial Abnormalities - complications | Craniofacial Abnormalities - genetics | De Lange Syndrome - genetics | Disease Models, Animal | Animals, Newborn | Embryo, Mammalian - pathology | De Lange Syndrome - physiopathology | Gene Expression Regulation | Heart Defects, Congenital - pathology | Bone Development | Transcription Factors - genetics | Mutation - genetics | Embryo, Mammalian - abnormalities | Phenotype | Animals | Heart Defects, Congenital - complications | Nervous System Malformations - complications | Survival Analysis | De Lange Syndrome - complications | Heterozygote | Heart Defects, Congenital - physiopathology | Mice | Bone and Bones - abnormalities | De Lange Syndrome - pathology | Proteins | Video recordings | Colleges & universities | Birth defects | Mutation | Behavior | Experiments | Chromosomes | DNA repair
Journal Article
Nature, ISSN 0028-0836, 2012, Volume 486, Issue 7405, pp. 104 - 108
Journal Article
2018, Methods in Molecular Biology, ISBN 149397713X, Volume 1752
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