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  • 1-10 ل  421 نتائج ل ""Genes, Modifier""

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Academic Journal

Modifier Factors of Cystic Fibrosis Phenotypes: A Focus on Modifier Genes.

  • Authors : Mésinèle J; Sorbonne Université, Inserm U938, Centre de Recherche Saint-Antoine (CRSA), 75012 Paris, France.; Inovarion, 75005 Paris, France.

Subjects: Cystic Fibrosis*/Cystic Fibrosis*/Cystic Fibrosis*/complications ; Cystic Fibrosis*/Cystic Fibrosis*/Cystic Fibrosis*/genetics ; Genes, Modifier*

  • Source: International journal of molecular sciences [Int J Mol Sci] 2022 Nov 17; Vol. 23 (22). Date of Electronic Publication: 2022 Nov 17.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene.

  • Authors : Mori M; Department of NeuroHealth Innovation, Institute for Biomedical Sciences, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University, Matsumoto, 390-8621, Japan. .; Department of Aging Biology, Shinshu University Graduate School of Medicine, Science and Technology, Matsumoto, 390-8621, Japan. .

Subjects: Cataract*/Cataract*/Cataract*/genetics ; Genes, Modifier*; Serine Proteases/Serine Proteases/Serine Proteases/*genetics

  • Source: Mammalian genome : official journal of the International Mammalian Genome Society [Mamm Genome] 2022 Sep; Vol. 33 (3), pp. 451-464. Date of Electronic Publication: 2022 Jan 24.Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9100916 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Hyperhaemolysis in a pregnant woman with a homozygous β 0 -thalassemia mutation and two genetic modifiers.

  • Authors : Jiwu L; Prenatal Diagnostic Center, Dongguan Maternal & Children Health Hospital, Dongguan, China.; Manna S

Subjects: Genes, Modifier*; beta-Globins/beta-Globins/beta-Globins/*genetics ; beta-Thalassemia/beta-Thalassemia/beta-Thalassemia/*genetics

  • Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Jul; Vol. 9 (7), pp. e1696. Date of Electronic Publication: 2021 May 07.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Combination of myeloproliferative neoplasm driver gene activation with mutations of splice factor or epigenetic modifier genes increases risk of rapid blastic progression.

  • Authors : Bartels S; Institut für Pathologie, Medizinische Hochschule Hannover, Hannover, Germany.; Vogtmann J

Subjects: Epigenesis, Genetic* ; Genes, Modifier* ; Mutation*

  • Source: European journal of haematology [Eur J Haematol] 2021 Apr; Vol. 106 (4), pp. 520-528. Date of Electronic Publication: 2021 Feb 01.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1600-0609

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Academic Journal

Genetic Modifiers of Hereditary Neuromuscular Disorders and Cardiomyopathy.

  • Authors : Bazrafshan S; Heart, Lung and Vascular Institute, Division of Cardiovascular Health and Disease, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.; Kushlaf H

Subjects: Genes, Modifier*; Cardiomyopathies/Cardiomyopathies/Cardiomyopathies/*genetics ; Neuromuscular Diseases/Neuromuscular Diseases/Neuromuscular Diseases/*genetics

  • Source: Cells [Cells] 2021 Feb 08; Vol. 10 (2). Date of Electronic Publication: 2021 Feb 08.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409

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Academic Journal

A breeding strategy to identify modifiers of high genetic risk for methamphetamine intake.

  • Authors : Reed C; Department of Behavioral Neuroscience and Methamphetamine Abuse Research Center, Oregon Health & Science University, Portland, Oregon, USA.; Stafford AM

Subjects: Genes, Modifier* ; Selective Breeding*; Amphetamine-Related Disorders/Amphetamine-Related Disorders/Amphetamine-Related Disorders/*genetics

  • Source: Genes, brain, and behavior [Genes Brain Behav] 2021 Feb; Vol. 20 (2), pp. e12667. Date of Electronic Publication: 2020Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B.

  • Authors : Becker T; Institute for Community Medicine, Ernst Moritz Arndt University, Greifswald, Germany.; xValue GmbH, Villich, Germany.

Subjects: Disease Susceptibility* ; Genes, Modifier* ; Siblings*

  • Source: Scientific reports [Sci Rep] 2020 Dec 31; Vol. 10 (1), pp. 22447. Date of Electronic Publication: 2020 Dec 31.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

New Omics-Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype?

  • Authors : Donato L; Department of Biomedical and Dental Sciences and Morphofunctional Imaging, Division of Medical Biotechnologies and Preventive Medicine, University of Messina, 98125 Messina, Italy.; Department of Biomolecular Strategies, Genetics and Avant-Garde Therapies, I.E.ME.S.T., 90139 Palermo, Italy.

Subjects: Genes, Modifier* ; Phenotype*; Ion Channels/Ion Channels/Ion Channels/*genetics

  • Source: International journal of molecular sciences [Int J Mol Sci] 2020 Dec 23; Vol. 22 (1). Date of Electronic Publication: 2020 Dec 23.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Exploiting codon usage identifies intensity-specific modifiers of Ras/MAPK signaling in vivo.

  • Authors : Sawyer JK; Department of Pharmacology & Cancer Biology, Duke University School of Medicine, Durham, North Carolina, United States of America.; Kabiri Z

Subjects: Codon Usage* ; Genes, Modifier*; Drosophila Proteins/Drosophila Proteins/Drosophila Proteins/*genetics

  • Source: PLoS genetics [PLoS Genet] 2020 Dec 09; Vol. 16 (12), pp. e1009228. Date of Electronic Publication: 2020 Dec 09 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

The GENDULF algorithm: mining transcriptomics to uncover modifier genes for monogenic diseases.

  • Authors : Auslander N; Cancer Data Science Laboratory (CDSL), National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.

Subjects: Algorithms* ; Data Mining* ; Genes, Modifier*

  • Source: Molecular systems biology [Mol Syst Biol] 2020 Dec; Vol. 16 (12), pp. e9701.Publisher: EMBO Press Country of Publication: Germany NLM ID: 101235389 Publication Model: Print Cited Medium: Internet ISSN: 1744-4292

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  • 1-10 ل  421 نتائج ل ""Genes, Modifier""