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Wyszukujesz frazę ""Justice CM"" wg kryterium: Autor


Wyświetlanie 1-15 z 15
Tytuł:
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428.
Autorzy:
Musolf AM; Statistical Genetics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Baltimore, MD, 21224, USA.
Justice CM; Neurobehavioral Clinical Research Section, Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, MD, 20892, USA.
Erdogan-Yildirim Z; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, 15219, USA.
Goovaerts S; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Department of Electrical Engineering, ESAT-PSI, KU Leuven, Leuven, Belgium.; Medical Imaging Research Center, University Hospitals Leuven, Leuven, Belgium.
Cuellar A; Department of Pediatrics, University of California Davis, Sacramento, CA, 95817, USA.
Shaffer JR; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, 15219, USA.; Department of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Marazita ML; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, 15219, USA.; Department of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Claes P; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Department of Electrical Engineering, ESAT-PSI, KU Leuven, Leuven, Belgium.; Medical Imaging Research Center, University Hospitals Leuven, Leuven, Belgium.
Weinberg SM; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, 15219, USA.; Department of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15213, USA.
Li J; Bioinformatics Core, Genome Center, University of California Davis, Davis, CA, 95618, USA.
Senders C; Department of Otolaryngology, Head and Neck Surgery, University of California Davis, Sacramento, CA, 95817, USA.
Zwienenberg M; Department of Neurosurgery, University of California Davis, Sacramento, CA, 95817, USA.
Simeonov E; Pediatric Clinic, Alexandrovska University Hospital, Medical University of Sofia, 1431, Sofia, Bulgaria.
Kaneva R; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, 1431, Sofia, Bulgaria.
Roscioli T; Neuroscience Research Australia, University of New South Wales, Sydney, Australia.
Di Pietro L; Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, 00168, Rome, Italy.; Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168, Rome, Italy.
Barba M; Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, 00168, Rome, Italy.; Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168, Rome, Italy.
Lattanzi W; Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, 00168, Rome, Italy.; Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168, Rome, Italy.
Cunningham ML; Seattle Children's Craniofacial Center, Center of Developmental Biology and Regenerative Medicine and Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA, 98105, USA.
Romitti PA; Department of Epidemiology, College of Public Health, The University of Iowa, Iowa City, IA, 52242, USA. .
Boyadjiev SA; Department of Pediatrics, University of California Davis, Sacramento, CA, 95817, USA.
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Źródło:
Scientific reports [Sci Rep] 2024 Apr 12; Vol. 14 (1), pp. 8533. Date of Electronic Publication: 2024 Apr 12.
Typ publikacji:
Journal Article
MeSH Terms:
Craniosynostoses*/genetics
Genome-Wide Association Study*
Humans ; Alleles ; Bone Morphogenetic Protein 2/genetics ; DNA, Intergenic/genetics ; Whole Genome Sequencing ; RNA, Long Noncoding
Czasopismo naukowe
Tytuł:
Antibodies to histone in the pediatric population: a retrospective chart review.
Autorzy:
Justice CM; Division of Rheumatology and Pediatric Rheumatology, Saint Louis University School of Medicine, St. Louis, MO, USA. .
Moore TL; Division of Rheumatology and Pediatric Rheumatology, Saint Louis University School of Medicine, St. Louis, MO, USA.
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Źródło:
Pediatric rheumatology online journal [Pediatr Rheumatol Online J] 2023 Apr 25; Vol. 21 (1), pp. 40. Date of Electronic Publication: 2023 Apr 25.
Typ publikacji:
Journal Article
MeSH Terms:
Lupus Erythematosus, Systemic*/diagnosis
Arthritis, Rheumatoid*
Adult ; Humans ; Child ; Histones/adverse effects ; Retrospective Studies ; Autoantibodies ; Antibodies, Antinuclear
Czasopismo naukowe
Tytuł:
Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis.
Autorzy:
Justice CM; Genometrics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland 21224 .
Bishop K; Zebrafish Core, Translational and Functional Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892.
Carrington B; Zebrafish Core, Translational and Functional Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892.
Mullikin JC; National Institutes of Health Intramural Sequencing Center, National Human Genome Research Institute, National Institutes of Health, Rockville, Maryland 20852.
Swindle K; Department of Orthopedic Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045.
Marosy B; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224.
Sood R; Zebrafish Core, Translational and Functional Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892.
Miller NH; Department of Orthopedic Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045.
Wilson AF; Genometrics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland 21224.
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2016 Jun 01; Vol. 6 (6), pp. 1707-12. Date of Electronic Publication: 2016 Jun 01.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Intramural; Research Support, N.I.H., Extramural
MeSH Terms:
Chromosomes, Human, Pair 5*
Conserved Sequence*
Genetic Predisposition to Disease*
Homeodomain Proteins/*genetics
Kyphosis/*genetics
Scoliosis/*genetics
Animals ; Animals, Genetically Modified ; Exons ; Gene Expression ; Genes, Reporter ; Genetic Association Studies ; Genotype ; Homeodomain Proteins/chemistry ; Humans ; Polymorphism, Single Nucleotide ; Zebrafish
Czasopismo naukowe
Tytuł:
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
Autorzy:
Justice CM; Genometrics Section, Inherited Disease Research Branch, Division of Intramural Research, National Human Genome Research Institute, US National Institutes of Health (NIH), Baltimore, MD, USA.
Yagnik G
Kim Y
Peter I
Jabs EW
Erazo M
Ye X
Ainehsazan E
Shi L
Cunningham ML
Kimonis V
Roscioli T
Wall SA
Wilkie AO
Stoler J
Richtsmeier JT
Heuzé Y
Sanchez-Lara PA
Buckley MF
Druschel CM
Mills JL
Caggana M
Romitti PA
Kay DM
Senders C
Taub PJ
Klein OD
Boggan J
Zwienenberg-Lee M
Naydenov C
Kim J
Wilson AF
Boyadjiev SA
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Źródło:
Nature genetics [Nat Genet] 2012 Dec; Vol. 44 (12), pp. 1360-4. Date of Electronic Publication: 2012 Nov 18.
Typ publikacji:
Journal Article; Research Support, American Recovery and Reinvestment Act; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Genetic Loci*
Genetic Predisposition to Disease*
Genome-Wide Association Study*
Bone Morphogenetic Protein 2/*genetics
Craniosynostoses/*genetics
Neoplasm Proteins/*genetics
Cohort Studies ; Cytoskeletal Proteins ; Humans ; Infant, Newborn ; Male ; Oligonucleotide Array Sequence Analysis ; Polymorphism, Single Nucleotide ; Sex Factors ; White People/genetics
Czasopismo naukowe
Tytuł:
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.
Autorzy:
Simpson CL; Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Justice CM; Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Krishnan M; Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Wojciechowski R; Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Sung H; Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Cai J; Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Green T; Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Lewis D; Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Behneman D; Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Wilson AF; Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
Bailey-Wilson JE; Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.
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Źródło:
BMC proceedings [BMC Proc] 2011 Nov 29; Vol. 5 Suppl 9, pp. S83. Date of Electronic Publication: 2011 Nov 29.
Typ publikacji:
Journal Article
Czasopismo naukowe
    Wyświetlanie 1-15 z 15

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