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Tytuł:
In-Depth Sequence Analysis of Bread Wheat VRN1 Genes.
Autorzy:
Strejčková B; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.; Department of Cell Biology and Genetics, Faculty of Science, Palacký University, 78371 Olomouc, Czech Republic.
Milec Z; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.
Holušová K; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.
Cápal P; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.
Vojtková T; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.
Čegan R; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.; Department of Plant Developmental Genetics, Institute of Biophysics of the Czech Academy of Sciences, 61200 Brno, Czech Republic.
Šafář J; Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Nov 13; Vol. 22 (22). Date of Electronic Publication: 2021 Nov 13.
Typ publikacji:
Journal Article
MeSH Terms:
Alleles*
Gene Dosage*
Genetic Variation*
Polyploidy*
Repressor Proteins/*genetics
Triticum/*genetics
Alternative Splicing ; Bread ; Mutagenesis, Insertional ; Sequence Analysis, DNA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genomic Aberrations Associated with the Pathophysiological Mechanisms of Neurodevelopmental Disorders.
Autorzy:
Yamamoto T; Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo 162-8666, Japan.
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Źródło:
Cells [Cells] 2021 Sep 04; Vol. 10 (9). Date of Electronic Publication: 2021 Sep 04.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Child Development*
Chromosome Aberrations*
Chromosomes, Human*
Genetic Variation*
Neurodevelopmental Disorders/*genetics
Neurodevelopmental Disorders/*physiopathology
Age Factors ; Animals ; Child ; Child, Preschool ; DNA Copy Number Variations ; Gene Dosage ; Genetic Predisposition to Disease ; Genetic Testing ; Haploinsufficiency ; Humans ; Infant ; Loss of Function Mutation ; Neurodevelopmental Disorders/diagnosis ; Phenotype ; Predictive Value of Tests ; Risk Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Population genomics and haplotype analysis in spelt and bread wheat identifies a gene regulating glume color.
Autorzy:
Abrouk M; Center for Desert Agriculture, Biological and Environmental Science and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Athiyannan N; Center for Desert Agriculture, Biological and Environmental Science and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Müller T; Department of Plant and Microbial Biology, University of Zurich, Zollikerstrasse 107, Zurich, Switzerland.
Pailles Y; Center for Desert Agriculture, Biological and Environmental Science and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Stritt C; Department of Plant and Microbial Biology, University of Zurich, Zollikerstrasse 107, Zurich, Switzerland.
Roulin AC; Department of Plant and Microbial Biology, University of Zurich, Zollikerstrasse 107, Zurich, Switzerland.
Chu C; Texas A&M AgriLife Research, Amarillo, TX, USA.
Liu S; Texas A&M AgriLife Research, Amarillo, TX, USA.
Morita T; Department of Agricultural and Life Sciences, Kyoto Prefectural University, Kyoto, Japan.
Handa H; Laboratory of Plant Breeding, Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto, Japan.
Poland J; Department of Plant Pathology, Kansas State University, Manhattan, KS, USA.
Keller B; Department of Plant and Microbial Biology, University of Zurich, Zollikerstrasse 107, Zurich, Switzerland.
Krattinger SG; Center for Desert Agriculture, Biological and Environmental Science and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia. .
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Źródło:
Communications biology [Commun Biol] 2021 Mar 19; Vol. 4 (1), pp. 375. Date of Electronic Publication: 2021 Mar 19.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Color*
Genetic Variation*
Genome, Plant*
Haplotypes*
Metagenomics*
Plant Proteins/*genetics
Transcription Factors/*genetics
Triticum/*genetics
Chromosomes, Plant ; DNA Copy Number Variations ; Gene Dosage ; Gene Expression Regulation, Plant ; Genome-Wide Association Study ; High-Throughput Nucleotide Sequencing ; Phenotype ; Plant Proteins/metabolism ; Polymorphism, Single Nucleotide ; Transcription Factors/metabolism ; Triticum/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
High gene flow maintains genetic diversity following selection for high EPSPS copy number in the weed kochia (Amaranthaceae).
Autorzy:
Martin SL; Agriculture and Agri-Food Canada, Ottawa Research and Development Centre, 960 Carling Avenue, Ottawa, ON, Canada. .
Benedict L; Agriculture and Agri-Food Canada, Ottawa Research and Development Centre, 960 Carling Avenue, Ottawa, ON, Canada.
Wei W; State Key Laboratory of Vegetation and Environmental Change, Institute of Botany, Chinese Academy of Sciences, Beijing, China.
Sauder CA; Agriculture and Agri-Food Canada, Ottawa Research and Development Centre, 960 Carling Avenue, Ottawa, ON, Canada.
Beckie HJ; Australian Herbicide Resistance Initiative, School of Agriculture and Environment, University of Western Australia, Perth, Australia.
Hall LM; Agricultural Food and Nutritional Science, University of Alberta, Edmonton, AB, Canada.
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Źródło:
Scientific reports [Sci Rep] 2020 Nov 02; Vol. 10 (1), pp. 18864. Date of Electronic Publication: 2020 Nov 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chenopodiaceae/*genetics
Genetic Variation/*genetics
Herbicide Resistance/*genetics
3-Phosphoshikimate 1-Carboxyvinyltransferase/genetics ; Canada ; Chenopodiaceae/drug effects ; DNA Copy Number Variations/genetics ; Gene Amplification/drug effects ; Gene Dosage/genetics ; Gene Expression Regulation, Plant/drug effects ; Gene Flow ; Glycine/analogs & derivatives ; Glycine/pharmacology ; Herbicides/pharmacology ; Glyphosate
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Expanded genome-wide comparisons give novel insights into population structure and genetic heterogeneity of Leishmania tropica complex.
Autorzy:
Salloum T; Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Byblos, Lebanon.
Moussa R; Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Byblos, Lebanon.
Rahy R; Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Byblos, Lebanon.
Al Deek J; Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Byblos, Lebanon.
Khalifeh I; Department of Pathology and Laboratory Medicine, American University of Beirut, Beirut, Lebanon.
El Hajj R; Department of Pathology and Laboratory Medicine, American University of Beirut, Beirut, Lebanon.
Hall N; Earlham Institute, Norwich research Park, University of East Anglia, Norwich, United Kingdom.
Hirt RP; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Tokajian S; Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Byblos, Lebanon.
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Źródło:
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2020 Sep 18; Vol. 14 (9), pp. e0008684. Date of Electronic Publication: 2020 Sep 18 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
Genome, Protozoan*
Leishmania tropica/*genetics
Azerbaijan ; DNA Copy Number Variations ; DNA, Protozoan/genetics ; Gene Dosage ; Geographic Mapping ; Humans ; Lebanon ; Leishmaniasis, Cutaneous/parasitology ; Leishmaniasis, Cutaneous/pathology ; Microsatellite Repeats ; Phylogeny ; Polymorphism, Single Nucleotide ; Refugees ; Syria
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Phased Genotyping-by-Sequencing Enhances Analysis of Genetic Diversity and Reveals Divergent Copy Number Variants in Maize.
Autorzy:
Manching H; Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19716.
Sengupta S; Program of Computational Genomics and Medicine, North Shore University Health System, Evanston, Illinois 60201.
Hopper KR; Beneficial Insect Introductions Research Unit, United States Department of Agriculture, Agricultural Research Service, Newark, Delaware 19713.
Polson SW; Center for Bioinformatics and Computational Biology, Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19711.
Ji Y; Program of Computational Genomics and Medicine, North Shore University Health System, Evanston, Illinois 60201.; Department of Health Studies, University of Chicago, Illinois 60637.
Wisser RJ; Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19716 .
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2017 Jul 05; Vol. 7 (7), pp. 2161-2170. Date of Electronic Publication: 2017 Jul 05.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Gene Dosage*
Genetic Loci*
Genetic Variation*
Linkage Disequilibrium*
Zea mays/*genetics
Genome-Wide Association Study
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
An Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human Health.
Autorzy:
Saitou M; State University of New York at Buffalo, Buffalo, USA. .
Gokcumen O; State University of New York at Buffalo, Buffalo, USA. .
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Źródło:
Journal of molecular evolution [J Mol Evol] 2020 Jan; Vol. 88 (1), pp. 104-119. Date of Electronic Publication: 2019 Sep 14.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Review
MeSH Terms:
DNA Copy Number Variations/*genetics
Disease/*genetics
Genetic Variation/*genetics
Biological Evolution ; Evolution, Molecular ; Gene Dosage/genetics ; Genome/genetics ; Genome-Wide Association Study/methods ; Genomics ; Genotype ; Haplotypes/genetics ; Health/trends ; Humans ; Phenotype ; Retroelements/genetics ; Selection, Genetic/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic regulatory variation in populations informs transcriptome analysis in rare disease.
Autorzy:
Mohammadi P; New York Genome Center, New York, NY, USA. .; Department of Systems Biology, Columbia University, New York, NY, USA.; Scripps Research Translational Institute, La Jolla, CA, USA.; Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA, USA.
Castel SE; New York Genome Center, New York, NY, USA.; Department of Systems Biology, Columbia University, New York, NY, USA.
Cummings BB; Analytical and Translation Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.; Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Einson J; New York Genome Center, New York, NY, USA.; Department of Systems Biology, Columbia University, New York, NY, USA.
Sousa C; Scripps Research Translational Institute, La Jolla, CA, USA.; Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA, USA.
Hoffman P; New York Genome Center, New York, NY, USA.; Department of Systems Biology, Columbia University, New York, NY, USA.
Donkervoort S; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Jiang Z; Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
Mohassel P; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Foley AR; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Wheeler HE; Department of Biology, Loyola University Chicago, Chicago, IL, USA.; Department of Computer Science, Loyola University Chicago, Chicago, IL, USA.
Im HK; Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
Bonnemann CG; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
MacArthur DG; Analytical and Translation Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.; Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Lappalainen T; New York Genome Center, New York, NY, USA. .; Department of Systems Biology, Columbia University, New York, NY, USA.
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Źródło:
Science (New York, N.Y.) [Science] 2019 Oct 18; Vol. 366 (6463), pp. 351-356. Date of Electronic Publication: 2019 Oct 10.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
Transcriptome*
Muscular Diseases/*genetics
Muscular Dystrophies/*genetics
Rare Diseases/*genetics
Gene Dosage ; Gene Expression Regulation ; Genome, Human ; Humans ; Models, Genetic ; Models, Statistical ; Quantitative Trait Loci
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic variation assessment of stacked-trait transgenic maize via conventional breeding.
Autorzy:
Wang X; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, MARA Key Laboratory on Safety Assessment (Molecular) of Agri-GMO, 12 Zhuangguancun South Street, Beijing, 100081, China.
Zhang X; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, MARA Key Laboratory on Safety Assessment (Molecular) of Agri-GMO, 12 Zhuangguancun South Street, Beijing, 100081, China.
Yang J; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, MARA Key Laboratory on Safety Assessment (Molecular) of Agri-GMO, 12 Zhuangguancun South Street, Beijing, 100081, China.
Liu X; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, MARA Key Laboratory on Safety Assessment (Molecular) of Agri-GMO, 12 Zhuangguancun South Street, Beijing, 100081, China.
Song Y; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, MARA Key Laboratory on Safety Assessment (Molecular) of Agri-GMO, 12 Zhuangguancun South Street, Beijing, 100081, China.
Wang Z; Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, MARA Key Laboratory on Safety Assessment (Molecular) of Agri-GMO, 12 Zhuangguancun South Street, Beijing, 100081, China. .
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Źródło:
BMC plant biology [BMC Plant Biol] 2019 Aug 07; Vol. 19 (1), pp. 346. Date of Electronic Publication: 2019 Aug 07.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Variation*
Plant Breeding*
Plants, Genetically Modified*
Zea mays/*genetics
China ; Food Safety ; Gene Dosage ; Genomic Instability ; Hazard Analysis and Critical Control Points ; Proteomics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Digital PCR for determination of cytochrome P450 2D6 and sulfotransferase 1A1 gene copy number variations.
Autorzy:
Motoi Y; Niigata University of Pharmacy and Applied Life Sciences.
Watanabe K; Hokkaido System Science Co., Ltd.
Honma H; Niigata University of Pharmacy and Applied Life Sciences.
Tadano Y; Niigata University of Pharmacy and Applied Life Sciences.
Hashimoto H; Hokkaido System Science Co., Ltd.
Kubota T; Niigata University of Pharmacy and Applied Life Sciences.
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Źródło:
Drug discoveries & therapeutics [Drug Discov Ther] 2017; Vol. 11 (6), pp. 336-341.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Dosage*
Genetic Variation*
Arylsulfotransferase/*genetics
Cytochrome P-450 CYP2D6/*genetics
Polymerase Chain Reaction/*methods
Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Selective sweep on human amylase genes postdates the split with Neanderthals.
Autorzy:
Inchley CE; Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 3QG, UK.
Larbey CD; Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 3QG, UK.
Shwan NA; School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham NG7 2UH, UK.; Scientific Research Centre, University of Salahaddin, Erbil, Kurdistan, Iraq.
Pagani L; Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 3QG, UK.; Estonian Biocentre, Tartu, 51010, Estonia.
Saag L; Estonian Biocentre, Tartu, 51010, Estonia.
Antão T; Division of Biological Sciences, University of Montana, Missoula, MT, USA.
Jacobs G; Complexity Institute, Nanyang Technological University, Singapore.
Hudjashov G; Estonian Biocentre, Tartu, 51010, Estonia.; Statistics and Bioinformatics Group, Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
Metspalu E; Estonian Biocentre, Tartu, 51010, Estonia.
Mitt M; Estonian Genome Center, University of Tartu, Tartu, Estonia.; Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Eichstaedt CA; Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 3QG, UK.; Thoraxclinic at the University Hospital Heidelberg, 69126 Heidelberg, Germany.
Malyarchuk B; Genetics Laboratory, Institute of Biological Problems of the North, Russian Academy of Sciences, Magadan, Russia.
Derenko M; Genetics Laboratory, Institute of Biological Problems of the North, Russian Academy of Sciences, Magadan, Russia.
Wee J; Division of Radiation Oncology, National Cancer Centre, Singapore.
Abdullah S; RIPAS Hospital, Bandar Seri Begawan, Brunei Darussalam.
Ricaut FX; Evolutionary Medicine group, Laboratoire d'Anthropologie Moléculaire et Imagerie de Synthèse, UMR 5288, Centre National de la Recherche Scientifique, Université de Toulouse 3, Toulouse, France.
Mormina M; Department of Applied Social Sciences, University of Winchester, Sparkford Road, Winchester SO22 4NR, UK.
Mägi R; Estonian Genome Center, University of Tartu, Tartu, Estonia.
Villems R; Estonian Biocentre, Tartu, 51010, Estonia.; Department of Evolutionary Biology, Institute of Molecular and Cell Biology, University of Tartu, 51010, Estonia.; Estonian Academy of Sciences, 10130 Tallinn, Estonia.
Metspalu M; Estonian Biocentre, Tartu, 51010, Estonia.
Jones MK; Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 3QG, UK.
Armour JA; School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham NG7 2UH, UK.
Kivisild T; Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 3QG, UK.; Estonian Biocentre, Tartu, 51010, Estonia.
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Źródło:
Scientific reports [Sci Rep] 2016 Nov 17; Vol. 6, pp. 37198. Date of Electronic Publication: 2016 Nov 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Evolution, Molecular*
Gene Dosage*
Genetic Variation*
Genome, Human*
Amylases/*genetics
Animals ; Female ; Humans ; Male ; Neanderthals
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Regional gender differences in an autosomal disease result in corresponding diversity differences.
Autorzy:
Guan S; Shenzhen University Health Sciences Center, School of Basic Medical Sciences, Department of Physiology, Shenzhen, 518061, China.; BGI-Yunnan, BGI-Shenzhen, Kunming, 650106, China.
Zhao Y; Shenzhen University Health Sciences Center, School of Basic Medical Sciences, Department of Physiology, Shenzhen, 518061, China.
Zhuo X; BGI-Yunnan, BGI-Shenzhen, Kunming, 650106, China.
Song W; BGI-Yunnan, BGI-Shenzhen, Kunming, 650106, China.
Geng X; Shenzhen Longgang ENT Institute, Shenzhen, 518100, China.
Yang H; BGI-Shenzhen, Shenzhen, 518083, China.; James D. Watson Institute of Genome Sciences, Hangzhou, 310058, China.
Wang J; BGI-Shenzhen, Shenzhen, 518083, China.; James D. Watson Institute of Genome Sciences, Hangzhou, 310058, China.
Wu X; Dali University First affiliated Hospital, Dali, 671000, China.
Yang J; BGI-Yunnan, BGI-Shenzhen, Kunming, 650106, China. .; Puer University, Puer School of BGI-Yunnan, Puer, 665000, China. .
Song X; The Third Affiliated Hospital of Kunming Medical University (Tumor Hospital of Yunnan Province), Kunming, 650000, China. .
Cheng L; BGI-Yunnan, BGI-Shenzhen, Kunming, 650106, China. .; Shenzhen Longgang ENT Institute, Shenzhen, 518100, China. .; Puer University, Puer School of BGI-Yunnan, Puer, 665000, China. .; Dali University, School of Basic Medical Sciences, Dali, 671003, China. .
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Źródło:
Scientific reports [Sci Rep] 2019 Apr 02; Vol. 9 (1), pp. 5472. Date of Electronic Publication: 2019 Apr 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
High-Throughput Nucleotide Sequencing/*methods
Thalassemia/*genetics
alpha-Globins/*genetics
beta-Globins/*genetics
China/ethnology ; Female ; Gene Dosage ; Humans ; Male ; Mutation ; Sequence Analysis, DNA ; Sex Characteristics ; Thalassemia/ethnology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Information about variations in multiple copies of bacterial 16S rRNA genes may aid in species identification.
Autorzy:
Ibal JC; School of Applied Biosciences, Kyungpook National University, Daegu, Republic of Korea.
Pham HQ; School of Applied Biosciences, Kyungpook National University, Daegu, Republic of Korea.
Park CE; School of Applied Biosciences, Kyungpook National University, Daegu, Republic of Korea.
Shin JH; School of Applied Biosciences, Kyungpook National University, Daegu, Republic of Korea.
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Źródło:
PloS one [PLoS One] 2019 Feb 15; Vol. 14 (2), pp. e0212090. Date of Electronic Publication: 2019 Feb 15 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
Bacteria/*classification
Bacteria/*genetics
Gene Dosage/*genetics
RNA, Ribosomal, 16S/*genetics
Base Sequence ; Sequence Analysis, RNA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Comparative plastid genomics of Synurophyceae: inverted repeat dynamics and gene content variation.
Autorzy:
Kim JI; Department of Biology, Chungnam National University, Daejeon, 34134, South Korea.
Shin H; Department of Biology, Chungnam National University, Daejeon, 34134, South Korea.
Škaloud P; Department of Botany, Faculty of Science, Charles University, Benátská 2, CZ-12800, Prague 2, Czech Republic.
Jung J; Department of General Education, Hongik University, Seoul, 04066, South Korea.
Yoon HS; Department of Biological Sciences, Sungkyunkwan University, Suwon, 16419, South Korea.
Archibald JM; Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, B3H 4R2, Canada. .
Shin W; Department of Biology, Chungnam National University, Daejeon, 34134, South Korea. .
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Źródło:
BMC evolutionary biology [BMC Evol Biol] 2019 Jan 11; Vol. 19 (1), pp. 20. Date of Electronic Publication: 2019 Jan 11.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
Genome, Plastid*
Genomics*
Inverted Repeat Sequences/*genetics
Stramenopiles/*genetics
Base Sequence ; DNA, Circular/genetics ; Evolution, Molecular ; Gene Dosage ; Nucleic Acid Conformation ; Phylogeny ; RNA, Transfer/chemistry ; RNA, Transfer/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Evolutionary diversity and novelty of DNA repair genes in asexual Bdelloid rotifers.
Autorzy:
Hecox-Lea BJ; Josephine Bay Paul Center for Comparative Molecular Biology and Evolution, Marine Biological Laboratory, Woods Hole, MA, USA.; Department of Biology, Northeastern University, Boston, MA, USA.
Mark Welch DB; Josephine Bay Paul Center for Comparative Molecular Biology and Evolution, Marine Biological Laboratory, Woods Hole, MA, USA. .
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Źródło:
BMC evolutionary biology [BMC Evol Biol] 2018 Nov 28; Vol. 18 (1), pp. 177. Date of Electronic Publication: 2018 Nov 28.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Evolution, Molecular*
Genetic Variation*
DNA Repair/*genetics
Reproduction, Asexual/*genetics
Rotifera/*genetics
Amino Acid Sequence ; Animals ; Conserved Sequence/genetics ; Gene Dosage ; Gene Transfer, Horizontal/genetics ; Phylogeny ; Proteins/chemistry ; Proteins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity.
Autorzy:
Petrovski S; Institute for Genomic Medicine, Columbia University, New York, New York, United States of America; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America; Department of Medicine, The University of Melbourne, Austin Health and Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Gussow AB; Institute for Genomic Medicine, Columbia University, New York, New York, United States of America; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America; Program in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina, United States of America.
Wang Q; Institute for Genomic Medicine, Columbia University, New York, New York, United States of America; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America.
Halvorsen M; Institute for Genomic Medicine, Columbia University, New York, New York, United States of America; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America.
Han Y; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America.
Weir WH; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America.
Allen AS; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America; Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, United States of America.
Goldstein DB; Institute for Genomic Medicine, Columbia University, New York, New York, United States of America; Center for Human Genome Variation, Duke University, School of Medicine, Durham, North Carolina, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2015 Sep 02; Vol. 11 (9), pp. e1005492. Date of Electronic Publication: 2015 Sep 02 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Dosage*
Genetic Variation*
Regulatory Sequences, Nucleic Acid*
DNA Copy Number Variations ; Haploinsufficiency ; Humans ; Mental Disorders/genetics ; Mutation ; Nervous System Diseases/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines.
Autorzy:
Houldcroft CJ; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom; Division of Biological Anthropology, Department of Archaeology and Anthropology, University of Cambridge, Cambridge, United Kingdom.
Petrova V; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
Liu JZ; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
Frampton D; Department of Infection, Division of Infection and Immunity, University College London, London, United Kingdom.
Anderson CA; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
Gall A; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
Kellam P; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom; Department of Infection, Division of Infection and Immunity, University College London, London, United Kingdom.
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Źródło:
PloS one [PLoS One] 2014 Oct 07; Vol. 9 (10), pp. e108384. Date of Electronic Publication: 2014 Oct 07 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Dosage*
Gene Expression Regulation*
Genetic Variation*
B-Lymphocytes/*metabolism
Epstein-Barr Virus Infections/*genetics
Herpesvirus 4, Human/*genetics
B-Lymphocytes/pathology ; B-Lymphocytes/virology ; Cell Line, Transformed ; Epstein-Barr Virus Infections/immunology ; Epstein-Barr Virus Infections/virology ; Genome-Wide Association Study ; Herpesvirus 4, Human/immunology ; Humans ; Polymorphism, Single Nucleotide ; Quantitative Trait Loci ; Transcriptome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Structural genomic variation in childhood epilepsies with complex phenotypes.
Autorzy:
Helbig I; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
Swinkels ME; 1] Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands [2] SEIN Epilepsy Institute in the Netherlands Foundation, Hoofddorp, The Netherlands.
Aten E; Department of Medical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Caliebe A; Department of Human Genetics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
van 't Slot R; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Boor R; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
von Spiczak S; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
Muhle H; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
Jähn JA; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
van Binsbergen E; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
van Nieuwenhuizen O; Department of Child Neurology, Rudolf Magnus Institute of Neurosciences, University Medical Center Utrecht, The Netherlands.
Jansen FE; Department of Child Neurology, Rudolf Magnus Institute of Neurosciences, University Medical Center Utrecht, The Netherlands.
Braun KP; Department of Child Neurology, Rudolf Magnus Institute of Neurosciences, University Medical Center Utrecht, The Netherlands.
de Haan GJ; SEIN Epilepsy Institute in the Netherlands Foundation, Hoofddorp, The Netherlands.
Tommerup N; Wilhelm Johannsen Centre for Functional Genome Research, Copenhagen, Denmark.
Stephani U; Department of Neuropediatrics, University Medical Center Schleswig-Holstein (UKSH), Kiel, Germany.
Hjalgrim H; 1] Danish Epilepsy Centre, Dianalund, Denmark [2] Institute of Regional Health Services Research, University of Southern Denmark, Odense, Denmark.
Poot M; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Lindhout D; 1] Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands [2] SEIN Epilepsy Institute in the Netherlands Foundation, Hoofddorp, The Netherlands.
Brilstra EH; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Møller RS; 1] Wilhelm Johannsen Centre for Functional Genome Research, Copenhagen, Denmark [2] Danish Epilepsy Centre, Dianalund, Denmark.
Koeleman BP; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
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Źródło:
European journal of human genetics : EJHG [Eur J Hum Genet] 2014 Jul; Vol. 22 (7), pp. 896-901. Date of Electronic Publication: 2013 Nov 27.
Typ publikacji:
Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
MeSH Terms:
Abnormalities, Multiple*/diagnostic imaging
Abnormalities, Multiple*/genetics
Epilepsy*/diagnostic imaging
Epilepsy*/genetics
Gene Dosage*
Genetic Variation*
Magnetic Resonance Imaging*
Phenotype*
Adolescent ; Adult ; Child, Preschool ; Female ; Genome-Wide Association Study ; Humans ; Infant ; Male ; Radiography
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Insights into the prevalence and underlying causes of clonal variation through transcriptomic analysis in Pichia pastoris.
Autorzy:
Aw R; Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK.; Centre for Synthetic Biology and Innovation, Imperial College London, London, SW7 2AZ, UK.
Barton GR; Centre for Integrative Systems Biology and Bioinformatics, Imperial College London, London, SW7 2AZ, UK.
Leak DJ; Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK. .; Department of Biology & Biochemistry, University of Bath, Bath, BA2 7AY, UK. .
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Źródło:
Applied microbiology and biotechnology [Appl Microbiol Biotechnol] 2017 Jun; Vol. 101 (12), pp. 5045-5058. Date of Electronic Publication: 2017 May 22.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Expression Profiling*
Gene Expression Regulation, Fungal*
Genetic Variation*
Pichia/*genetics
Proteins/*genetics
Endoplasmic Reticulum/metabolism ; Gene Dosage ; Humans ; Pichia/physiology ; Protein Folding ; Proteins/chemistry ; Proteins/metabolism ; Recombinant Proteins/chemistry ; Recombinant Proteins/metabolism ; Serum Albumin/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
CNVs-microRNAs interactions demonstrate unique characteristics in the human genome. An interspecies in silico analysis.
Autorzy:
Dweep H; Medical Research Center, University of Heidelberg, Mannheim, Germany.
Georgiou GD
Gretz N
Deltas C
Voskarides K
Felekkis K
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Źródło:
PloS one [PLoS One] 2013 Dec 02; Vol. 8 (12), pp. e81204. Date of Electronic Publication: 2013 Dec 02 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Dosage*
Genetic Variation*
Genome, Human/*physiology
MicroRNAs/*genetics
Animals ; Cattle ; Chickens ; Dogs ; Humans ; Macaca ; Mice ; Pan troglodytes ; Rats ; Species Specificity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 1-20 z 246

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