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1998, Methods, a companion to methods in enzymology, Volume 14, no. 2., 105-235.
Book
MAMMALIAN GENOME, ISSN 0938-8990, 06/2019, Volume 30, Issue 5-6, pp. 89 - 89
Journal Article
Cellular Microbiology, ISSN 1462-5814, 01/2019, Volume 21, Issue 1, pp. e12960 - n/a
Non‐typeable Haemophilus influenzae (NTHi) is a major pathogen causing acute otitis media (AOM). The relationship between the cellular content of the middle... 
ACUTE OTITIS-MEDIA | MONOCYTES | EFFUSION | MICROBIOLOGY | CYTOKINE | ACTIVATING-FACTOR PAF | CHILDREN | CELL BIOLOGY | Health aspects | Analysis | Hemophilus infections | Flow cytometry | Computational fluid dynamics | Infections | Leukocytes (neutrophilic) | Necrosis | Monocytes | Inoculation | Fluids | Ear | Otitis media | Infiltration | Middle ear | Immune system
Journal Article
Mammalian Genome, ISSN 0938-8990, 8/2019, Volume 30, Issue 7, pp. 212 - 216
Surprisingly we remain ignorant of the function of the majority of genes in the human and mouse genomes. The dark genome is a major obstacle to the... 
Life Sciences | Human Genetics | Cell Biology | Animal Genetics and Genomics | EVOLVABILITY | CONSORTIUM | COMPLEX | GENETICS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | GENETICS & HEREDITY | GENOTYPE-PHENOTYPE MAP | DISCOVERY | Animal genetics | Genomes | Analysis | Genes | Genomics
Journal Article
by Dickinson, Mary E and Flenniken, Ann M and Ji, Xiao and Teboul, Lydia and Wong, Michael D and White, Jacqueline K and Meehan, Terrence F and Weninger, Wolfgang J and Westerberg, Henrik and Adissu, Hibret and Baker, Candice N and Bower, Lynette and Brown, James M and Caddle, L Brianna and Chiani, Francesco and Clary, Dave and Cleak, James and Daly, Mark J and Denegre, James M and Doe, Brendan and Dolan, Mary E and Edie, Sarah M and Fuchs, Helmut and Gailus-Durner, Valerie and Galli, Antonella and Gambadoro, Alessia and Gallegos, Juan and Guo, Shiying and Horner, Neil R and Hsu, Chih-Wei and Johnson, Sara J and Kalaga, Sowmya and Keith, Lance C and Lanoue, Louise and Lawson, Thomas N and Lek, Monkol and Mark, Manuel and Marschall, Susan and Mason, Jeremy and McElwee, Melissa L and Newbigging, Susan and Nutter, Lauryl M J and Peterson, Kevin A and Ramirez-Solis, Ramiro and Rowland, Douglas J and Ryder, Edward and Samocha, Kaitlin E and Seavitt, John R and Selloum, Mohammed and Szoke-Kovacs, Zsombor and Tamura, Masaru and Trainor, Amanda G and Tudose, Ilinca and Wakana, Shigeharu and Warren, Jonathan and Wendling, Olivia and West, David B and Wong, Leeyean and Yoshiki, Atsushi and MacArthur, Daniel G and Tocchini-Valentini, Glauco P and Gao, Xiang and Flicek, Paul and Bradley, Allan and Skarnes, William C and Justice, Monica J and Parkinson, Helen E and Moore, Mark and Wells, Sara and Braun, Robert E and Svenson, Karen L and de Angelis, Martin Hrabe and Herault, Yann and Mohun, Tim and Mallon, Ann-Marie and Henkelman, R Mark and Brown, Steve D M and Adams, David J and Lloyd, K C Kent and McKerlie, Colin and Beaudet, Arthur L and Bućan, Maja and Murray, Stephen A and Charles River Laboratories and RIKEN BioResource Center and International Mouse Phenotyping Consortium and Infrastructure Nationale PHENOMIN, Institut Clinique de la Souris (ICS) and Jackson Laboratory and MRC Harwell and Wellcome Trust Sanger Institute and Toronto Centre for Phenogenomics
Nature, 09/2016, Volume 537, Issue 7621, p. 508
Journal Article
Cell Reports, ISSN 2211-1247, 12/2018, Volume 25, Issue 12, pp. 3315 - 3328.e6
Mutations in genes essential for mitochondrial function have pleiotropic effects. The mechanisms underlying these traits yield insights into metabolic... 
adiposity | ISR | hypertrophic cardiomyopathy | mitochondrial dysfunction | deafness | pleiotropic | WARS2 | RESPIRATORY-CHAIN DEFICIENCY | HEARING-LOSS | HYPERTROPHIC CARDIOMYOPATHY | GENE | TRANSFER-RNA SYNTHETASE | LACTIC-ACIDOSIS | MUTATIONS | INDUCTION | MITOCHONDRIAL MYOPATHY | FGF21 | CELL BIOLOGY
Journal Article
by Dickinson, Mary E and Flenniken, Ann M and Ji, Xiao and Teboul, Lydia and Wong, Michael D and White, Jacqueline K and Meehan, Terrence F and Weninger, Wolfgang J and Westerberg, Henrik and Adissu, Hibret and Baker, Candice N and Bower, Lynette and Brown, James M and Caddle, L. Brianna and Chiani, Francesco and Clary, Dave and Cleak, James and Daly, Mark J and Denegre, James M and Doe, Brendan and Dolan, Mary E and Edie Helmut Fuchs, Sarah M and Gailus-Durner, Valerie and Galli, Antonella and Gambadoro, Alessia and Gallegos, Juan and Guo, Shiying and Horner, Neil R and Hsu, Chih-Wei and Johnson, Sara J and Kalaga, Sowmya and Keith, Lance C and Lanoue, Louise and Lawson, Thomas N and Lek, Monkol and Mark, Manuel and Marschall, Susan and Mason, Jeremy and McElwee, Melissa L and Nutter, Susan Newbigging Lauryl M. J and Peterson, Kevin A and Ramirez-Solis, Ramiro and Rowland, Douglas J and Ryder, Edward and Samocha, Kaitlin E and Seavitt, John R and Selloum, Mohammed and Szoke-Kovacs, Zsombor and Tamura, Masaru and Trainor, Amanda G and Tudose, Ilinca and Wakana, Shigeharu and Warren, Jonathan and Wendling, Olivia and West, David B and Wong, Leeyean and Yoshiki, Atsushi and Wurst, Wolfgang and MacArthur, Daniel G and Tocchini-Valentini, Glauco P and Gao, Xiang and Flicek, Paul and Bradley, Allan and Skarnes, William C and Justice, Monica J and Parkinson, Helen E and Moore, Mark and Wells, Sara and Braun, Robert E and Svenson, Karen L and de Angelis, Martin Hrabe and Herault, Yann and Mohun, Tim and Mallon, Ann-Marie and Henkelman, R. Mark and Brown, Steve D. M and Adams, David J and Lloyd, K. C. Kent and McKerlie, Colin and Beaudet, Arthur L and Murray, Maja Bućan Stephen A and The International Mouse Phenotyping Consortium
Nature, ISSN 0028-0836, 11/2017, Volume 551, Issue 7680, pp. 398 - 398
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 02/2012, Volume 27, Issue 2, pp. 413 - 428
Progeny of mice treated with the mutagen N‐ethyl‐N‐nitrosourea (ENU) revealed a mouse, designated Longpockets (Lpk), with short humeri, abnormal vertebrae, and... 
SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA | OSTEOARTHRITIS | DISORGANIZED GROWTH PLATE | TYPE II COLLAGEN | N‐ETHYL‐N‐NITROSOUREA | N-ETHYL-N-NITROSOUREA | C-PROPEPTIDE | II COLLAGEN DISORDER | ALKALINE-PHOSPHATASE | EPIPHYSEAL DYSPLASIA | PHENOTYPIC SPECTRUM | PROCOLLAGEN GENE | SPONDYLOPERIPHERAL DYSPLASIA | ENDOCRINOLOGY & METABOLISM | DISPROPORTIONATE MICROMELIA DMM | MISSENSE MUTATION | MUTAGENESIS PROGRAM | Growth Plate - pathology | Chromosomes, Mammalian - genetics | Genetic Loci - genetics | Molecular Sequence Data | Male | Mutation, Missense - genetics | Growth Plate - abnormalities | Osteochondrodysplasias - genetics | Base Sequence | Chondrocytes - metabolism | Disease Models, Animal | Osteoarthritis - complications | Amino Acid Sequence | Chondrocytes - pathology | Embryo, Mammalian - pathology | Physical Chromosome Mapping | Mice, Inbred C57BL | Organ Size | Mutant Proteins - metabolism | Collagen Type II - genetics | Embryo, Mammalian - abnormalities | Osteoarthritis - genetics | Phenotype | Animals | Chondrocytes - ultrastructure | Osteochondrodysplasias - congenital | Collagen Type II - chemistry | Mice | Protein Processing, Post-Translational | Osteogenesis | Osteochondrodysplasias - complications | Animal models | Vertebrae | Spine | Embryos | Growth plate | Bone growth | Ethyl nitrosourea | Transfection | Computed tomography | Mutagens | Collagen | Chondrocytes | Bone mineral density | Mutation | Endoplasmic reticulum | Osteoarthritis | chromosome 15 | Vacuoles | Cartilage diseases | Index Medicus
Journal Article
Journal of Immunology, ISSN 0022-1767, 06/2012, Volume 188, Issue 12, pp. 6371 - 6380
Journal Article