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1. Full Text High-throughput discovery of novel developmental phenotypes
by Dickinson, Mary E and Ji, Xiao and Teboul, Lydia and Wong, Michael D and White, Jacqueline K and Meehan, Terrence F and Westerberg, Henrik and Adissu, Hibret and Baker, Candice N and Brianna Caddle, L and Chiani, Francesco and Clary, Dave and Cleak, James and Daly, Mark J and Denegre, James M and Edie, Sarah M and Gailus-Durner, Valerie and Galli, Antonella and Gambadoro, Alessia and Gallegos, Juan and Johnson, Sara J and Lawson, Thomas N and Lek, Monkol and Mason, Jeremy and McElwee, Melissa L and Nutter, Lauryl M.J and Rowland, Douglas J and Samocha, Kaitlin E and Seavitt, John R and Szoke-Kovacs, Zsombor and Trainor, Amanda G and Wakana, Shigeharu and Warren, Jonathan and West, David B and Tocchini-Valentini, Glauco P 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 Svenson, Karen L and Herault, Yann and Mallon, Ann-Marie and Mark Henkelman, R and Brown, Steve D.M and Adams, David J and Kent Lloyd, K.C and McKerlie, Colin and Urban, Barbara and Lund, Caroline and LaCasse, Taylor and Mehalow, Adrienne and Taft, Robert and Kutney, Peter and Goodwin, Leslie and Kales, Susan and Urban, Rachel and Palmer, Kristina and Pertuy, Fabien and Bitz, Deborah and Weber, Bruno and Jacobs, Hughes and Ennah, Hamid and Ali-Hadji, Dalila and Wattenhofer-Donze, Marie and André, Philippe and Birling, Marie-Christine and Pavlovic, Guillaume and Sorg, Tania and Morse, Iva and Benso, Frank and Harrison, Jackie and Guo, Ruolin and Qu, Dawei and Spring, Shoshana and Ellegood, Jacob and Shang, Xueyuan and Feugas, Pat and Creighton, Amie and Penton, Patricia Castellanos and Danisment, Ozge and Griggs, Nicola and Tudor, Catherine L and Green, Angela L and Icoresi Mazzeo, Cecilia and Siragher, Emma and Lillistone, Charlotte and Gleeson, Diane and Sethi, Debarati and Bayzetinova, Tanya and Burvill, Jonathan and Habib, Bishoy and Maswood, Ryea and Woods, Michael and Grau, Evelyn and Sinclair, Caroline and Brown, Ellen and Ayabe, Shinya and Int Mouse Phenotyping Consortium and The International Mouse Phenotyping Consortium
Nature (London), ISSN 0028-0836, 09/2016, Volume 537, Issue 7621, pp. 508 - 514
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic research | Phenotype | Research | High-throughput screening (Biochemical assaying) | Methods | Genotype & phenotype | Disease | Developmental biology | Genes | Genomes | Mutation | Embryos | Index Medicus | knockout | embryonic lethal | mouse | KOMP | IMPC | EUCOMM
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2. Full Text Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repair
by Low, Benjamin E and Krebs, Mark P and Joung, J. Keith and Tsai, Shengdar Q and Nishina, Patsy M and Wiles, Michael V
Investigative ophthalmology & visual science, ISSN 0146-0404, 12/2013, Volume 55, Issue 1, pp. 387 - 395
Genetic engineering | KOMP | Gene therapy | TALEN | CRB1 associated disease | Embryonic Stem Cells - metabolism | Retina - metabolism | Recombinational DNA Repair - genetics | Retinal Degeneration - genetics | Tomography, Optical Coherence | Nerve Tissue Proteins - genetics | Retinal Degeneration - metabolism | Nerve Tissue Proteins - metabolism | Microscopy, Confocal | Phenotype | Animals | Retinal Degeneration - therapy | Alleles | Polymerase Chain Reaction | Mice, Inbred C57BL - genetics | Female | Mice | Mutation | Eye Proteins | Retina - pathology | Disease Models, Animal | Genetic Therapy - methods | Index Medicus | gene therapy | genetic engineering
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3. Full Text Feasibility for a large scale mouse mutagenesis by injecting CRISPR/Cas plasmid into zygotes
by Mashiko, Daisuke and Young, Samantha A. M and Muto, Masanaga and Kato, Hirotaka and Nozawa, Kaori and Ogawa, Masaki and Noda, Taichi and Kim, Yeon‐Joo and Satouh, Yuhkoh and Fujihara, Yoshitaka and Ikawa, Masahito
Development, growth & differentiation, ISSN 0012-1592, 01/2014, Volume 56, Issue 1, pp. 122 - 129
knockout | Eucomm | International Knockout Mouse Consortium | International Mouse Phenotyping Consortium | Knockout mouse project, KOMP | Knockout | Life Sciences & Biomedicine | Developmental Biology | Science & Technology | Cell Biology | Gene Targeting - methods | Animals | Mice, Mutant Strains | Humans | HEK293 Cells | Plasmids - genetics | Zygote - metabolism | Mutagenesis, Site-Directed - methods | Mice | Mutation - genetics | CRISPR-Cas Systems - genetics | Feasibility Studies | Animal genetics | Fluorescence | Genomics | Index Medicus
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4. Fuzzy rough FMEA evaluation method based on hybrid multi-attribute decision and correlative analysis
by An, Xianghua and Yu, Jingbo and Cai, Weiguo
Jisuanji Jicheng Zhizao Xitong/Computer Integrated Manufacturing Systems, CIMS, ISSN 1006-5911, 11/2016, Volume 22, Issue 11, pp. 2613 - 2621
Automata-analytical hierarchy process | Failure mode and effects analysis | Complex network | Vlsekriterijumska optimizacija-komp-romisno resenje | Fuzzy rough number
Journal Article
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5. Full Text Whole exome sequencing reveals a functional mutation in the GAIN domain of the Bai2 receptor underlying a forward mutagenesis hyperactivity QTL
by Speca, David J and Trimmer, James S and Peterson, Andrew S and Díaz, Elva
Mammalian genome, ISSN 0938-8990, 12/2017, Volume 28, Issue 11, pp. 465 - 475
Life Sciences | Human Genetics | Cell Biology | Animal Genetics and Genomics | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Quantitative genetics | Physiological aspects | Mice | G proteins | Cells | Neurophysiology | Membrane proteins | Mental disorders | Hyperactivity | Exons | Cloning | Cell surface | Quantitative trait loci | Angiogenesis | Missense mutation | Ethyl nitrosourea | Mutagenesis | Cell lines | Mutation | Gene mapping | Locomotor activity | Index Medicus | Adgrb2tm1b(KOMP)Mbp | ENU mutagenesis | International Mouse Phenotyping Consortium (IMPC) | Bai2 | Adgrb2m1Djs | QTL | GAIN domain
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6. A window to heaven
: when children see life in death
by Komp, Diane M
1992, ISBN 9780310589709, 125
Consolation | Christianity | Religious aspects | Children and death | Komp, Diane M
Book
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7. Full Text Disrupting the male germ line to find infertility and contraception targets
by Archambeault, Denise R and Matzuk, Martin M
Annales d'endocrinologie, ISSN 0003-4266, 2014, Volume 75, Issue 2, pp. 101 - 108
Internal Medicine | Endocrinology & Metabolism | Germ cell | Spermatogenèse | KOMP | Spermatogenesis | Infertility | Infertilité | CRISPR-Cas | Cellule germinale | Contraception | KOMP2 | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Gynecology. Andrology. Obstetrics | Birth control | Vertebrates: endocrinology | Biological and medical sciences | Medical sciences | Sterility. Assisted procreation | Mice, Knockout - genetics | Spermatogenesis - genetics | Antispermatogenic Agents - isolation & purification | Humans | Genomic Library | Male | Spermatozoa - metabolism | Gene Knockout Techniques | Fertility - genetics | Phenotype | Animals | Mutagenesis | CRISPR-Cas Systems | Mice | Genes, Reporter | Disease Models, Animal
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8. Full Text Alkylglycerone phosphate synthase (AGPS) deficient mice: Models for rhizomelic chondrodysplasia punctata type 3 (RCDP3) malformation syndrome
by Liegel, Ryan P and Ronchetti, Adam and Sidjanin, D.J
Molecular genetics and metabolism reports, ISSN 2214-4269, 2014, Volume 1, Issue 1, pp. 299 - 311
Phenotype | Mutation | Mouse | Hypomorphic | RCDP3 | AGPS
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9. Full Text Kernel Sparse Representation for Anomaly Detection in Hyperspectral Imagery
by Xiong, Jie and Ling, Qiang and Lin, Zaiping and Wu, Jing
Proceedings of the 2nd International Conference on advances in image processing, 06/2018, pp. 106 - 110
KOMP | Anomaly detection | hyperspectral imagery | sparse representation | Sparse representation | Hyperspectral imagery
Conference Proceeding
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10. Full Text Los indonesios, optimistas por su nuevo presidente confían convertirse en una gran potencia
by MARCRI
Portafolio, 10/2014
Komp, Johannes
Trade Publication Article
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11. Full Text A. S. Pushkin, “Evgenii Oniegin,” Igra dlia personal´nago komp´iutera (review)
by Cooper, David L
Pushkin review, ISSN 1526-1476, 2011, Volume 14, Issue 1, pp. 165 - 167
Dreamlore | A. S. Pushkin, “Evgenii Oniegin,” Igra dlia personal´nago komp´iutera | Social life and customs | Fiction | Russia
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12. Full Text The blessings and curses of C57BL/6 substrains in mouse genetic studies
by Bryant, Camron D
Annals of the New York Academy of Sciences, ISSN 0077-8923, 12/2011, Volume 1245, Issue 1, pp. 31 - 33
KOMP | inbred | next‐generation sequencing | QTL mapping | Inbred | Next-generation sequencing | Mice, Knockout - genetics | Phenotype | Animals | Species Specificity | Mice, Inbred C57BL - classification | Mice, Inbred C57BL - genetics | Mice | Polymorphism, Single Nucleotide | Mice, Knockout - classification | Animal genetics | Quantitative genetics | Genetic research | Genetics | Index Medicus
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13. Full Text Screening Gene Knockout Mice for Variation in Bone Mass: Analysis by μCT and Histomorphometry
by Rowe, David W and Adams, Douglas J and Hong, Seung-Hyun and Zhang, Caibin and Shin, Dong-Guk and Renata Rydzik, C and Chen, Li and Wu, Zhihua and Garland, Gaven and Godfrey, Dana A and Sundberg, John P and Ackert-Bicknell, Cheryl
Current osteoporosis reports, ISSN 1544-1873, 4/2018, Volume 16, Issue 2, pp. 77 - 94
Bone phenotyping | μCT | Medicine & Public Health | Orthopedics | Web portal | Histomorphometry | Epidemiology | IMPC and KOMP | Severity of Illness Index | Bone and Bones - pathology | Femur - pathology | Genotype | Femur - diagnostic imaging | Sex Characteristics | X-Ray Microtomography | Mice, Knockout | Phenotype | Program Development | Spine - diagnostic imaging | Animals | Bone and Bones - diagnostic imaging | Information Management | Mice | Spine - pathology | Databases, Factual | Index Medicus
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14. Full Text CRISPR/Cas9-Mediated insertion of loxP sites in the mouse Dock7 gene provides an effective alternative to use of targeted embryonic stem cells
by Bishop, Kathleen A and Harrington, Anne and Kouranova, Evguenia and Weinstein, Edward J and Rosen, Clifford J and Cui, Xiaoxia and Liaw, Lucy
G3 (Bethesda, Md.), ISSN 2160-1836, 07/2016, Volume 6, Issue 7, pp. 2051 - 2061
CRISPR/Cas9 | Dock7 | KOMP ES cells | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Embryonic Stem Cells - metabolism | Gene Targeting - methods | Endonucleases - genetics | Embryonic Stem Cells - cytology | RNA, Guide - genetics | Exons | RNA, Guide - metabolism | Zygote - metabolism | Endonucleases - metabolism | Base Sequence | DNA End-Joining Repair | Clustered Regularly Interspaced Short Palindromic Repeats | Female | Guanine Nucleotide Exchange Factors - deficiency | Guanine Nucleotide Exchange Factors - genetics | Microinjections | Zygote - cytology | Mice, Inbred C57BL | Gene Editing | Mice, Knockout | Animals | Alleles | CRISPR-Cas Systems | Mice | Mutagenesis, Insertional | Index Medicus
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15. Full Text William H. W. Komp. May 2 (legislative day, March 5), 1946. -- Ordered to be printed
by Ellender, Allen Joseph
1946, United States congressional serial set, Volume serial set no. 11015, 5
Allowances (Pay) | Komp, William H.W | Legislative Report - Private Bills | Claims | United States | Public Health Service | Government employees and officials
eBook
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16. Full Text William H.W. Komp. March 19, 1946. -- Committed to the Committee of the Whole House and ordered to be printed
by Combs, Jesse Martin
1946, United States congressional serial set, Volume serial set no. 11023, 5
Allowances (Pay) | Komp, William H.W | Legislative Report - Private Bills | Claims | United States | Public Health Service | Government employees and officials
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17. Full Text Mouse resources for craniofacial research
by Murray, Stephen A
Genesis (New York, N.Y. : 2000), ISSN 1526-954X, 04/2011, Volume 49, Issue 4, pp. 190 - 199
knockout | FaceBase | KOMP | Cre | Knockout | Genetics & Heredity | Life Sciences & Biomedicine | Developmental Biology | Science & Technology | International Cooperation | Mice, Mutant Strains - physiology | Mutation - genetics | Mice, Mutant Strains - genetics | Skull - embryology | Phenotype | Animals | Maxillofacial Development - physiology | Skull - anatomy & histology | Integrases - metabolism | Models, Animal | Mice | Internet | Craniofacial Abnormalities - genetics | Databases, Factual | Index Medicus
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