المؤلفون: Reiner, Alexander P, Lettre, Guillaume, Nalls, Michael A, Ganesh, Santhi K, Mathias, Rasika, Austin, Melissa A, Dean, Eric, Arepalli, Sampath, Britton, Angela, Chen, Zhao, Couper, David, Curb, J David, Eaton, Charles B, Fornage, Myriam, Grant, Struan FA, Harris, Tamara B, Hernandez, Dena, Kamatini, Naoyuki, Keating, Brendan J, Kubo, Michiaki, LaCroix, Andrea, Lange, Leslie A, Liu, Simin, Lohman, Kurt, Meng, Yan, Mohler, Emile R, Musani, Solomon, Nakamura, Yusuke, O'Donnell, Christopher J, Okada, Yukinori, Palmer, Cameron D, Papanicolaou, George J, Patel, Kushang V, Singleton, Andrew B, Takahashi, Atsushi, Tang, Hua, Taylor, Herman A, Taylor, Kent, Thomson, Cynthia, Yanek, Lisa R, Yang, Lingyao, Ziv, Elad, Zonderman, Alan B, Folsom, Aaron R, Evans, Michele K, Liu, Yongmei, Becker, Diane M, Snively, Beverly M, Wilson, James G

المصدر: PLoS genetics. 7(6)

مصطلحات موضوعية: Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 4, Chromosomes, Human, Pair 16, Humans, Microfilament Proteins, Receptors, Cell Surface, Duffy Blood-Group System, Leukocyte Count, Artifacts, Reproducibility of Results, DNA Replication, Phenotype, Polymorphism, Single Nucleotide, African Americans, Asian Continental Ancestry Group, European Continental Ancestry Group, Chemokine CXCL2, Genome-Wide Association Study, Molecular Epidemiology, Genetic Loci, Chromosomes, Human, Pair 1, Pair 4, Pair 16, Receptors, Cell Surface, Polymorphism, Single Nucleotide, Genetics, Developmental Biology

الوصول الحر: https://escholarship.org/uc/item/2b30d3vbTest

المؤلفون: Reich, David, Nalls, Michael A, Kao, WH Linda, Akylbekova, Ermeg L, Tandon, Arti, Patterson, Nick, Mullikin, James, Hsueh, Wen-Chi, Cheng, Ching-Yu, Coresh, Josef, Boerwinkle, Eric, Li, Man, Waliszewska, Alicja, Neubauer, Julie, Li, Rongling, Leak, Tennille S, Ekunwe, Lynette, Files, Joe C, Hardy, Cheryl L, Zmuda, Joseph M, Taylor, Herman A, Ziv, Elad, Harris, Tamara B, Wilson, James G

المصدر: PLoS genetics. 5(1)

مصطلحات موضوعية: Neutrophils, Chromosomes, Human, Pair 1, Humans, Receptors, Cell Surface, Duffy Blood-Group System, Leukocyte Count, Case-Control Studies, Cohort Studies, Genotype, Phenotype, Polymorphism, Single Nucleotide, Adult, Aged, Aged, 80 and over, Middle Aged, African Continental Ancestry Group, European Continental Ancestry Group, Female, Male, and over, Chromosomes, Human, Pair 1, Polymorphism, Single Nucleotide, Receptors, Cell Surface, Genetics, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/1mw0393pTest

المؤلفون: Fan, Qiao, Barathi, Veluchamy, Cheng, Ching-Yu, Zhou, Xin, Meguro, Akira, Nakata, Isao, Khor, Chiea-Chuen, Goh, Liang-Kee, Li, Yi-Ju, Lim, Wane, Ho, Candice, Hawthorne, Felicia, Zheng, Yingfeng, Chua, Daniel, Inoko, Hidetoshi, Yamashiro, Kenji, Ohno-Matsui, Kyoko, Matsuo, Keitaro, Matsuda, Fumihiko, Vithana, Eranga, Mizuki, Nobuhisa, Beuerman, Roger, Tai, E-Shyong, Yoshimura, Nagahisa, Aung, Tin, Young, Terri, Wong, Tien-Yin, Teo, Yik-Ying, Saw, Seang-Mei, Seielstad, Mark

المصدر: PLoS Genetics. 8(6)

مصطلحات موضوعية: Adult, Animals, Carrier Proteins, Cation Transport Proteins, Child, China, Chromosomes, Human, Pair 1, Disease Models, Animal, Female, Gene Expression, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Lysophospholipase, Male, Mice, Middle Aged, Myopia, Nuclear Proteins, Polymorphism, Single Nucleotide, RNA-Binding Proteins, Retina, Retinal Pigment Epithelium, Sclera, Zinc Transporter 8

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4gn6x10xTest
https://escholarship.org/content/qt4gn6x10x/qt4gn6x10x.pdfTest

المؤلفون: Bernardo Lemos, Shoukai Yu

المصدر: PLoS Genetics
PLoS Genetics, Vol 14, Iss 3, p e1007258 (2018)

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Nucleolus, Gene Expression, Genome, Biochemistry, Genetics (clinical), Energy-Producing Organelles, Oligonucleotide Array Sequence Analysis, Gene Ontologies, Gene Expression Regulation, Developmental, Genomics, Chromatin, Mitochondria, Nucleic acids, Ribosomal RNA, Chromosomes, Human, Pair 1, Pseudogenes, Research Article, Cell biology, Cellular structures and organelles, lcsh:QH426-470, Pseudogene, Computational biology, Biology, Bioenergetics, Genome Complexity, DNA, Ribosomal, Genomic Instability, Human Genomics, 03 medical and health sciences, Protein Domains, Gene Types, Centromere, Genetics, Humans, Homeobox, Non-coding RNA, Molecular Biology, Ribosomal DNA, Gene, Ecology, Evolution, Behavior and Systematics, Cell Nucleus, Binding Sites, Genome, Human, Biology and Life Sciences, Computational Biology, Proteins, Genome Analysis, lcsh:Genetics, 030104 developmental biology, RNA, Ribosomes

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddae0e9e8891af0cc7ebafc7ce7a1b76Test
https://pubmed.ncbi.nlm.nih.gov/29570716Test

المؤلفون: Shota Yamakoshi, Ikuko Maejima, Satoshi Tsukamoto, Hisae Kobayashi, Mika Tsunoda, Ken Sato, Taichi Hara, Rika Hirai, Satoshi Oikawa, Aguri Ono, Tomoko Akuzawa

المصدر: PLoS Genetics
PLoS Genetics, Vol 14, Iss 9, p e1007647 (2018)

مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, Cell, Cell Membranes, Receptors, Cytoplasmic and Nuclear, Chromosome Disorders, Immunostaining, Mice, Neural Stem Cells, Cell Signaling, Medicine and Health Sciences, Receptor, Genetics (clinical), Cerebral Cortex, Mice, Knockout, Notch Signaling, Staining, Membrane Glycoproteins, Behavior, Animal, Receptors, Notch, Gene Expression Regulation, Developmental, Brain, Neural stem cell, Cell biology, Immunoblot Analysis, medicine.anatomical_structure, Cerebral cortex, Chromosomes, Human, Pair 1, Female, Chromosome Deletion, Anatomy, Cellular Structures and Organelles, Research Article, Signal Transduction, lcsh:QH426-470, Notch signaling pathway, Molecular Probe Techniques, Biology, Research and Analysis Methods, 03 medical and health sciences, Cell Line, Tumor, Genetics, medicine, Animals, Humans, Molecular Biology Techniques, Immunohistochemistry Techniques, Molecular Biology, Cerebrum, Ecology, Evolution, Behavior and Systematics, Endoplasmic reticulum, Biology and Life Sciences, Membrane Proteins, Cell Biology, Histochemistry and Cytochemistry Techniques, lcsh:Genetics, Adaptor Proteins, Vesicular Transport, Disease Models, Animal, 030104 developmental biology, Membrane protein, Cell culture, Specimen Preparation and Treatment, Immunologic Techniques, Amyloid Precursor Protein Secretases, CRISPR-Cas Systems, Lysosomes

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8c71aa74790be69629b7a65969fd2dTest
https://pubmed.ncbi.nlm.nih.gov/30260951Test

المؤلفون: Mary E. Comeau, Patrick M. Gaffney, Miranda C. Marion, Jennifer M. Grossman, Adam Adler, Elizabeth E. Brown, Kathy L. Moser, Gary S. Gilkeson, Lindsey A. Criswell, Anne M. Stevens, Carl D. Langefeld, Chack-Yung Yu, Bernardo A. Pons-Estel, Kenneth M. Kaufman, Yeong Wook Song, Luis M. Vilá, Ji Ah Park, Timothy B. Niewold, Joel M. Guthridge, Juan-Manuel Anaya, So Young Bang, Diane L. Kamen, Timothy J. Vyse, Barry I. Freedman, Graciela S. Alarcón, Julie T. Ziegler, Timothy H.J. Goodship, Nan Shen, Judith A. James, Melanie Khosravi, Rita M. Cantor, Eun Young Lee, Soo-Kyung Cho, Stuart B. Glenn, Xiaoxia Qian, Marta E. Alarcón-Riquelme, Jennifer A. Kelly, Susan A. Boackle, Michelle Petri, Bevra H. Hahn, Joan T. Merrill, R. Hal Scofield, Robert P. Kimberly, Betty P. Tsao, Chaim O. Jacob, Rosalind Ramsey-Goldman, Hui Wu, Adrienne H. Williams, Jian Zhao, John D. Reveille, John B. Harley, Deh Ming Chang, Huijuan Cui, Jeffrey C. Edberg, Sang Cheol Bae

المساهمون: UCL - SSS/IREC/RUMA - Pôle de Pathologies rhumatismales, UCL - (SLuc) Service de rhumatologie

المصدر: PLoS Genetics
PLoS Genetics, Vol 7, Iss 5, p e1002079 (2011)
PLoS Genetics, Vol. 7, no. 5, p. e1002079 (2011)
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario

مصطلحات موضوعية: Cancer Research, Unclassified drug, Complement System, 0302 clinical medicine, Gene Frequency, Lupus Erythematosus, Systemic, Genetics (clinical), Genetics, Chromosomes, Human, Pair 1 - genetics, 0303 health sciences, Intergenic SNP, Lupus Erythematosus, Systemic - ethnology, genetics, Hispanic or Latino, 3. Good health, European Continental Ancestry Group - genetics, Chromosomes, Human, Pair 1, Factor H, Complement Factor H, Hispanic Americans - genetics, Medicine, Research Article, lcsh:QH426-470, Genotype, Inmunología, Single-nucleotide polymorphism, Complement factor H, Biology, Polymorphism, Single Nucleotide, White People, Autoimmune Diseases, 03 medical and health sciences, African Americans - genetics, Asian People, Antigens, Neoplasm, Lupus eritematoso sistémico, medicine, Biomarkers, Tumor, Humans, Tumor marker, Genetic Predisposition to Disease, Complement regulator factor H related protein, Allele, Molecular Biology, Allele frequency, Ecology, Evolution, Behavior and Systematics, Alleles, Genetic Association Studies, 030304 developmental biology, 030203 arthritis & rheumatology, Complement regulator factor H related protein 2, Bladder tumor associated antigen, Lupus erythematosus, Complement regulator factor H related protein 1, Lupus Erythematosus, Complement Factor H - genetics, Haplotype, Human Genetics, medicine.disease, Enfermedades, Genética, Introns, Plasma protein, Complement system, Black or African American, lcsh:Genetics, Asian Continental Ancestry Group - genetics, Genes, Antigens, Neoplasm - genetics, Case-Control Studies, Immune System, Tumor Markers, Biological - genetics, Clinical Immunology, Tumor antigen, Gene Deletion

وصف الملف: Recurso electrónico; application/pdf; Documento

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84182131cb87181575477f803e6c4a2eTest
https://pubmed.ncbi.nlm.nih.gov/21637784Test

المؤلفون: Jonathon G. Keeney, Veronica B. Searles, Jonathan M. Davis, James M. Sikela, Nathan Anderson, Laura Dumas

المصدر: PLoS Genetics, Vol 10, Iss 3, p e1004241 (2014)
PLoS Genetics

مصطلحات موضوعية: Male, Cancer Research, genetic structures, Gene Dosage, Developmental and Pediatric Neurology, Pediatrics, Behavioral Neuroscience, 0302 clinical medicine, Gene Duplication, Gene duplication, Copy-number variation, Child, Genetics (clinical), Genetics, 0303 health sciences, Brain, Genomics, Functional Genomics, Autism spectrum disorder, Chromosomes, Human, Pair 1, Child, Preschool, Brain size, Medicine, Female, Research Article, Adult, Adolescent, DNA Copy Number Variations, lcsh:QH426-470, Biology, behavioral disciplines and activities, 03 medical and health sciences, Text mining, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Autistic Disorder, Molecular Biology, Gene, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, business.industry, Infant, medicine.disease, DUF1220, Protein Structure, Tertiary, lcsh:Genetics, Autism, business, 030217 neurology & neurosurgery, Neuroscience

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::836483210b9b6ae479ee56e674e65efcTest
http://europepmc.org/articles/PMC3961203?pdf=renderTest

المؤلفون: Akira Meguro, Keitaro Matsuo, Hidetoshi Inoko, Eranga N. Vithana, Mark Seielstad, Liang Kee Goh, Qiao Fan, Terri L. Young, Isao Nakata, Roger W. Beuerman, Xin Zhou, Tien Yin Wong, Kenji Yamashiro, Ching-Yu Cheng, E. Shyong Tai, Seang-Mei Saw, Kyoko Ohno-Matsui, Candice E H Ho, Wan’E. Lim, Veluchamy A. Barathi, Yi-Ju Li, Felicia Hawthorne, Tin Aung, Yik Ying Teo, Daniel Chua, Chiea Chuen Khor, Fumihiko Matsuda, Yingfeng Zheng, Nagahisa Yoshimura, Nobuhisa Mizuki

المصدر: PLoS Genetics, Vol 8, Iss 6, p e1002753 (2012)
PLoS Genetics

مصطلحات موضوعية: Male, Cancer Research, genetic structures, Gene Expression, Genome-wide association study, Retinal Pigment Epithelium, Mice, 0302 clinical medicine, Polymorphism (computer science), Myopia, Child, Cation Transport Proteins, Genetics (clinical), Genetics, 0303 health sciences, Nuclear Proteins, RNA-Binding Proteins, Middle Aged, 3. Good health, Sclera, medicine.anatomical_structure, Chromosomes, Human, Pair 1, Medicine, Female, Lysophospholipase, Research Article, Adult, China, medicine.medical_specialty, lcsh:QH426-470, Zinc Transporter 8, Biology, Polymorphism, Single Nucleotide, Retina, 03 medical and health sciences, Ophthalmology, Genome-Wide Association Studies, medicine, Animals, Humans, Genetic Predisposition to Disease, Allele, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genetic association, Retinal pigment epithelium, Chromosome, eye diseases, Minor allele frequency, Disease Models, Animal, lcsh:Genetics, Genetics of Disease, 030221 ophthalmology & optometry, sense organs, Carrier Proteins, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::794fec6c6592ff7ed5f0ab0f942b04f0Test
http://europepmc.org/articles/PMC3369958?pdf=renderTest

المؤلفون: Elad Ziv, Christopher J. O'Donnell, Alexander P. Reiner, Brendan J. Keating, Cameron D. Palmer, Eric Dean, Kushang V. Patel, David Couper, Yukinori Okada, Sampath Arepalli, Emile R. Mohler, George J. Papanicolaou, Zhao Chen, Lisa R. Yanek, Cynthia A. Thomson, Angela Britton, Atsushi Takahashi, Lingyao Yang, Aaron R. Folsom, Kent D. Taylor, Guillaume Lettre, Michele K. Evans, J. David Curb, Yusuke Nakamura, Simin Liu, Dena G. Hernandez, Yongmei Liu, Kurt Lohman, Yan Meng, Charles B. Eaton, Hua Tang, Solomon K. Musani, Melissa A. Austin, Myriam Fornage, James G. Wilson, Alan B. Zonderman, Struan F.A. Grant, Andrew B. Singleton, Tamara B. Harris, Diane M. Becker, Michiaki Kubo, Rasika A. Mathias, Santhi K. Ganesh, Naoyuki Kamatini, Leslie A. Lange, Mike A. Nalls, Andrea Z. LaCroix, Herman A. Taylor, Beverly M. Snively

المساهمون: Abecasis, Gonçalo R

المصدر: PLoS Genetics, Vol 7, Iss 6, p e1002108 (2011)
PLoS genetics, vol 7, iss 6

مصطلحات موضوعية: Cancer Research, Chemokine CXCL2, Genome-wide association study, QH426-470, Leukocyte Count, 0302 clinical medicine, Receptors, Genetics (clinical), Segmental duplication, Genetics, African Americans, 0303 health sciences, education.field_of_study, Molecular Epidemiology, Microfilament Proteins, Single Nucleotide, 3. Good health, Phenotype, Pair 4, 030220 oncology & carcinogenesis, Cell Surface, Pair 1, Artifacts, Human, Asian Continental Ancestry Group, DNA Replication, Population, European Continental Ancestry Group, Locus (genetics), Biology, Chromosomes, White People, 03 medical and health sciences, Asian People, SNP, Humans, Polymorphism, education, Molecular Biology, Genotyping, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Pair 16, Prevention, Human Genome, Chromosome, Reproducibility of Results, Black or African American, Genetic epidemiology, Genetic Loci, Duffy Blood-Group System, Genome-Wide Association Study, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887fb319d7f89ff9d037f8a7a4b12911Test
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21738479/?tool=EBITest

المؤلفون: Vincent Plagnol, Joanna M M Howson, Deborah J Smyth, Neil Walker, Jason P Hafler, Chris Wallace, Helen Stevens, Laura Jackson, Matthew J Simmonds, Type 1 Diabetes Genetics Consortium, Polly J Bingley, Stephen C Gough, John A Todd

المصدر: PLoS Genetics
PLoS Genetics, Vol 7, Iss 8, p e1002216 (2011)

مصطلحات موضوعية: Cancer Research, lcsh:QH426-470, endocrine system diseases, Adolescent, Graves' disease, Immunology, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, Genome-wide association study, Autoimmunity, Human leukocyte antigen, Major histocompatibility complex, Polymorphism, Single Nucleotide, ABO Blood-Group System, 03 medical and health sciences, 0302 clinical medicine, Antigen, Thyroid peroxidase, medicine, Genetics, Genome-Wide Association Studies, Genetics of the Immune System, Humans, Receptors, Immunologic, Child, Molecular Biology, Biology, Genetics (clinical), Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Autoantibodies, 0303 health sciences, biology, Autoantibody, Membrane Proteins, medicine.disease, C420 Human Genetics, Graves Disease, 3. Good health, lcsh:Genetics, Diabetes Mellitus, Type 1, Chromosomes, Human, Pair 1, Child, Preschool, biology.protein, Chromosomes, Human, Pair 9, Genome-Wide Association Study, Research Article

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50bc8524e30aae2aca792986de896efcTest
https://pubmed.ncbi.nlm.nih.gov/21829393Test