يعرض 1 - 9 نتائج من 9 نتيجة بحث عن '"Sean Woods"', وقت الاستعلام: 0.82s تنقيح النتائج
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    المساهمون: Hannes Tapani Lohi / Principal Investigator, Research Programs Unit, Veterinary Biosciences, Research Programme for Molecular Neurology, University of Helsinki, Veterinary Genetics, Medicum

    المصدر: Cell Reports, Vol 23, Iss 9, Pp 2643-2652 (2018)
    Cell reports, vol 23, iss 9
    Cell reports
    Kaukonen, Maria; Woods, Sean; Ahonen, Saija; Lemberg, Seppo; Hellman, Maarit; Hytönen, Marjo K; et al.(2018). Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease. Cell Reports, 23(9), 2643-2652. doi: 10.1016/j.celrep.2018.04.118. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/5rd6q428

    مصطلحات موضوعية: 0301 basic medicine, Male, Non-Mendelian inheritance, Protein Folding, congenital eye defect, Eye Diseases, genetic structures, NATIVE DISULFIDE BONDS, Medical Physiology, Retinoic acid, Reproductive health and childbirth, 413 Veterinary science, Microphthalmia, vitamin A, chemistry.chemical_compound, Plasma, A-vitamiini, 2.1 Biological and endogenous factors, Microphthalmos, Prealbumin, CRYSTAL-STRUCTURE, Aetiology, Base Pairing, lcsh:QH301-705.5, Sequence Deletion, Pediatric, whole genome sequencing, VITAMIN-A-DEFICIENCY, ANOPHTHALMIA, Penetrance, Pedigree, medicine.anatomical_structure, Phenotype, Female, medicine.medical_specialty, Genotype, ENDOPLASMIC-RETICULUM, Genes, Recessive, METABOLISM, Biology, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, Dogs, canine genetics, Internal medicine, Placenta, RETINOL-BINDING-PROTEIN, Genetics, medicine, Animals, Humans, Recessive, MALFORMATIONS, BIOCHEMICAL BASIS, Amino Acid Sequence, Allele, Eye Disease and Disorders of Vision, Nutrition, genome-wide association study, 030102 biochemistry & molecular biology, western blotting, MUTATIONS, ta1184, RBP4, maternal inheritance, medicine.disease, Retinol-Binding Proteins, Retinol binding protein, nuclear magnetic resonance, 030104 developmental biology, Endocrinology, chemistry, Genes, lcsh:Biology (General), microphthalmia, Genetic Loci, Hela Cells, 1182 Biochemistry, cell and molecular biology, Congenital Structural Anomalies, 3111 Biomedicine, Biochemistry and Cell Biology, Digestive Diseases, Genomic imprinting, Retinol-Binding Proteins, Plasma, HeLa Cells

    وصف الملف: application/pdf; fulltext

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    المصدر: Chou, Christopher M; Nelson, Christine; Tarlé, Susan A; Pribila, Jonathan T; Bardakjian, Tanya; Woods, Sean; et al.(2015). Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease.. Cell, 161(3), 634-646. doi: 10.1016/j.cell.2015.03.006. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/82f1x73r
    Cell, vol 161, iss 3

    وصف الملف: application/pdf

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    مورد إلكتروني

    المؤلفون: Biddle, Brad

    المساهمون: White, Andrew (VerfasserIn); Woods, Sean (VerfasserIn)

    المصدر: 2013