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by De Angelis, Martin Hrabě and Nicholson, George and Selloum, Mohammed and White, Jacqueline K and Morgan, Hugh and Ramirez-Solis, Ramiro and Sorg, Tania and Wells, Sara and Fuchs, Helmut and Fray, Martin and Adams, David J and Adams, Niels C and Adler, Thure and Aguilar-Pimentel, Antonio and Ali-Hadji, Dalila and Amann, Gregory and André, Philippe and Atkins, Sarah and Auburtin, Aurelie and Ayadi, Abdel and Becker, Julien and Becker, Lore and Bedu, Elodie and Bekeredjian, Raffi and Birling, Marie-Christine and Blake, Andrew and Bottomley, Joanna and Bowl, Michael R and Brault, Véronique and Busch, Dirk H and Bussell, James N and Calzada-Wack, Julia and Cater, Heather and Champy, Marie-France and Charles, Philippe and Chevalier, Claire and Chiani, Francesco and Codner, Gemma F and Combe, Roy and Cox, Roger and Dalloneau, Emilie and Dierich, André and Di Fenza, Armida and Doe, Brendan and Duchon, Arnaud and Eickelberg, Oliver and Esapa, Chris T and Fertak, Lahcen El and Feigel, Tanja and Emelyanova, Irina and Estabel, Jeanne and Favor, Jack and Flenniken, Ann and Gambadoro, Alessia and Garrett, Lilian and Gates, Hilary and Gerdin, Anna-Karin and Gkoutos, George and Greenaway, Simon and Glasl, Lisa and Goetz, Patrice and Da Cruz, Isabelle Goncalves and Götz, Alexander and Graw, Jochen and Guimond, Alain and Hans, Wolfgang and Hicks, Geoff and Hölter, Sabine M and Höfler, Heinz and Hancock, John M and Hoehndorf, Robert and Hough, Tertius and Houghton, Richard and Hurt, Anja and Ivandic, Boris and Jacobs, Hughes and Jacquot, Sylvie and Jones, Nora and Karp, Natasha A and Katus, Hugo A and Kitchen, Sharon and Klein-Rodewald, Tanja and Klingenspor, Martin and Klopstock, Thomas and Lalanne, Valerie and Leblanc, Sophie and Lengger, Christoph and Le Marchand, Elise and Ludwig, Tonia and Lux, Aline and McKerlie, Colin and Maier, Holger and Mandel, Jean-Louis and Marschall, Susan and Mark, Manuel and Melvin, David G and Meziane, Hamid and Micklich, Kateryna and Mittelhauser, Christophe and Monassier, Laurent and ... and EUMODIC Consortium
Nature Genetics, ISSN 1061-4036, 08/2015, Volume 47, Issue 9, pp. 969 - 978
The function of the majority of genes in the mouse and human genomes remains unknown. The mouse embryonic stem cell knockout resource provides a basis for the... 
EUROPHENOME | ANNOTATION | GENETICS & HEREDITY | GENOME-WIDE | EMPRESS | KNOCKOUT MICE | ACCESS | RESOURCE | Homozygote | Phenotype | Animals | Genetic Association Studies | Humans | Mice, Inbred C57BL | Molecular Sequence Annotation | Female | Heterozygote | Male | Mutation | Mice, Knockout | Research | Gene mutations | Human genome | Identification and classification | Health aspects | Consortia | Genotype & phenotype | Physiology | Genomes | Metabolism | Power
Journal Article
Journal Article
Journal Article
Mut.Res.-Genetic Toxicology and Environmental Mutagenesis, ISSN 1383-5718, 2011, Volume 720, Issue 1, pp. 1 - 2
Journal Article
Molecular Cancer, ISSN 1476-4598, 08/2014, Volume 13, Issue 1, p. 182
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 1931-857X, 11/2007, Volume 293, Issue 5, pp. 1736 - 1745
Vesico-ureteric reflux (VUR) is a urinary tract abnormality that affects roughly one-third of patients with renal-coloboma syndrome, an autosomal dominant... 
development | PHYSIOLOGY | URETERAL BUD | NEUROTROPHIC FACTOR | PAX2 | intravesical ureter | RENAL-COLOBOMA SYNDROME | NEPHRIC DUCT | GENE | ureteric bud | UROLOGY & NEPHROLOGY | MICE | KIDNEY | urinary tract maturation | TRANSCRIPTION FACTOR | EXPRESSION
Journal Article
Journal Article
Cell, ISSN 0092-8674, 2009, Volume 137, Issue 5, pp. 961 - 971
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e38310
Cln3(Delta ex7/8) mice harbor the most common genetic defect causing juvenile neuronal ceroid lipofuscinosis (JNCL), an autosomal recessive disease involving... 
V-ATPASE | BATTEN-DISEASE GENE | PROTEIN | ATRIAL-NATRIURETIC-PEPTIDE | INDEPENDENT MECHANISMS | JUVENILE | MITOCHONDRIAL | MULTIDISCIPLINARY SCIENCES | KNOCK-IN MICE | BETA-HEXOSAMINIDASE | NEURONAL CEROID-LIPOFUSCINOSIS | Immunohistochemistry | Molecular Chaperones - metabolism | Membrane Glycoproteins - metabolism | Male | Retinal Degeneration - etiology | Oxygen Consumption - physiology | Neuronal Ceroid-Lipofuscinoses - pathology | Exploratory Behavior - physiology | Neuronal Ceroid-Lipofuscinoses - genetics | Ferritins - blood | Female | Disease Models, Animal | Electroretinography | Neuronal Ceroid-Lipofuscinoses - complications | Heart - growth & development | Mice, Inbred C57BL | Molecular Chaperones - genetics | Neuronal Ceroid-Lipofuscinoses - metabolism | Organ Size | Genotype | Mice, Transgenic | Body Temperature | Membrane Glycoproteins - genetics | Lymphocytes - pathology | Phenotype | Animals | Analysis of Variance | Brain - pathology | Mice | Retinal Degeneration - pathology | Heart | Medical examination | Neurons | Analysis | Ferritin | T cells | Blood | Neonates | Pediatrics | Nephrology | Heart attacks | Peptides | Erythrocytes | Central nervous system | Cognitive ability | Retina | Biochemistry | Ultrasonic imaging | Epididymis | Hematopoiesis | Peripheral blood | Bioindicators | Young adults | Body temperature | Breeding of animals | Homozygotes | Neurology | Pathology | Hospitals | Rectum | Biomarkers | Adults | Mutation | Biomedical research | Lymphocytes T | Biology | Red blood cells | Immunology | Lymphocytes | Rodents | Neuronal ceroid lipofuscinosis | Heart diseases | Age | Seizures | Blood cells | Aquaporins | Oxygen consumption | Cystic fibrosis | Hemopoiesis | Medicine | Clear cells | Phenotyping | Genetic research | Sensorimotor integration | Psychiatry
Journal Article
Genetics, ISSN 0016-6731, 07/2008, Volume 179, Issue 3, pp. 1345 - 1355
Journal Article