يعرض 1 - 10 نتائج من 12 نتيجة بحث عن '"Membrane Proteins / genetics"', وقت الاستعلام: 0.83s تنقيح النتائج
  1. 1

    المساهمون: Experimental Vascular Medicine, ACS - Atherosclerosis & ischemic syndromes, ACS - Microcirculation, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism

    المصدر: Circulation, vol. 144, no. 20, pp. 1629-1645
    Circulation, 144(20), 1629-1645. Lippincott Williams and Wilkins
    Circulation

    وصف الملف: application/pdf

  2. 2

    المصدر: American journal of human genetics
    American journal of human genetics, vol. 99, no. 5, pp. 1190-1198

    مصطلحات موضوعية: Adult, Male, Uveal Neoplasms, Aged, Aged, 80 and over, Case-Control Studies, DNA Copy Number Variations, Eukaryotic Initiation Factor-1/genetics, Eukaryotic Initiation Factor-1/metabolism, Exons, Female, GTP-Binding Protein alpha Subunits/genetics, GTP-Binding Protein alpha Subunits/metabolism, GTP-Binding Protein alpha Subunits, Gq-G11/genetics, GTP-Binding Protein alpha Subunits, Gq-G11/metabolism, Genome-Wide Association Study, Humans, Melanocytes/pathology, Melanoma/diagnosis, Melanoma/genetics, Membrane Proteins/genetics, Membrane Proteins/metabolism, Middle Aged, Mutation, Phosphoproteins/genetics, Phosphoproteins/metabolism, RNA Splicing Factors/genetics, RNA Splicing Factors/metabolism, Skin Neoplasms, Tumor Suppressor Proteins/genetics, Tumor Suppressor Proteins/metabolism, Tumor Suppressor p53-Binding Protein 1/genetics, Tumor Suppressor p53-Binding Protein 1/metabolism, Ubiquitin Thiolesterase/genetics, Ubiquitin Thiolesterase/metabolism, Ubiquitin-Protein Ligases/genetics, Ubiquitin-Protein Ligases/metabolism, Uveal Neoplasms/diagnosis, Uveal Neoplasms/genetics, 0301 basic medicine, medicine.medical_specialty, Ubiquitin-Protein Ligases, Eukaryotic Initiation Factor-1, Uveal Neoplasm, Biology, medicine.disease_cause, 03 medical and health sciences, Report, Molecular genetics, Genetics, medicine, Melanoma, Genetics (clinical), Whole genome sequencing, GNA11, Tumor Suppressor Proteins, Membrane Proteins, Phosphoproteins, medicine.disease, GTP-Binding Protein alpha Subunits, 3. Good health, 030104 developmental biology, Cutaneous melanoma, GTP-Binding Protein alpha Subunits, Gq-G11, Melanocytes, RNA Splicing Factors, Tumor Suppressor p53-Binding Protein 1, Ubiquitin Thiolesterase, GNAQ

    وصف الملف: application/pdf

  3. 3

    المساهمون: Instituto de Investigação e Inovação em Saúde

    المصدر: Repositório Científico de Acesso Aberto de Portugal
    Repositório Científico de Acesso Aberto de Portugal (RCAAP)
    instacron:RCAAP

    مصطلحات موضوعية: 0301 basic medicine, Intracellular Membranes/metabolism, Peptide Fragments/metabolism, Peroxisome-Targeting Signal 1 Receptor, Receptors, Cytoplasmic and Nuclear/genetics, Amino Acid Motifs, Receptors, Cytoplasmic and Nuclear, Recombinant Proteins/chemistry, medicine.disease_cause, Biochemistry, Repressor Proteins/chemistry, Protein targeting, Lipid bilayer, Recombinant Proteins/metabolism, biology, Chemistry, Peroxisome, Recombinant Fusion Proteins/chemistry, Hydrogen-Ion Concentration, Translocon, Receptors, Cytoplasmic and Nuclear/metabolism, Recombinant Proteins, Recombinant Fusion Proteins/metabolism, Endopeptidase K, Receptor recycling, Peptide Fragments/chemistry, Recombinant Fusion Proteins, Mutation, Missense, Receptors, Cytoplasmic and Nuclear/chemistry, Models, Biological, 03 medical and health sciences, medicine, Peroxisomes, Humans, Protein Interaction Domains and Motifs, Membrane Proteins/genetics, Peptide Fragments/genetics, Molecular Biology, Repressor Proteins/genetics, Peroxisomal matrix, Peroxisomes/metabolism, Repressor Proteins/metabolism, Membrane Proteins/chemistry, Membrane Proteins, Biological Transport, Cell Biology, Intracellular Membranes, Proteinase K, Peptide Fragments, Repressor Proteins, Cytosol, 030104 developmental biology, Amino Acid Substitution, Solubility, Mutation, biology.protein, Biophysics, Mutagenesis, Site-Directed, Membrane Proteins/metabolism, Protein Multimerization, Gene Deletion, Endopeptidase K/metabolism

    وصف الملف: application/pdf

  4. 4

    المساهمون: Institut Cochin (IC UM3 (UMR 8104 / U1016)), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Physiopathologie et Pharmacotoxicologie Placentaire Humaine (U1139), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital de la Conception [CHU - APHM] (LA CONCEPTION), Vascular research center of Marseille (VRCM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU), Nutrition, obésité et risque thrombotique (NORT), Institut National de la Recherche Agronomique (INRA)-Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université de Caen Normandie - UFR Santé (UNICAEN Santé), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU), Innovations thérapeutiques en hémostase (IThEM - U1140), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Descartes - Paris 5 (UPD5), Hôpital de la Conception [CHU - APHM] (LA CONCEPTION ), Aix Marseille Université (AMU)-Institut National de la Recherche Agronomique (INRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)

    المصدر: PloS one, vol. 12, no. 10, pp. e0186321
    PLoS ONE
    PLoS ONE, Public Library of Science, 2017, 12 (10), pp.e0186321. ⟨10.1371/journal.pone.0186321⟩
    PLoS ONE, 2017, 12 (10), pp.e0186321. ⟨10.1371/journal.pone.0186321⟩
    PLoS ONE, Vol 12, Iss 10, p e0186321 (2017)

    مصطلحات موضوعية: 0301 basic medicine, Male, Angiogenesis, Physiology, lcsh:Medicine, Blood Pressure, Cardiovascular Physiology, Biochemistry, Vascular Medicine, Epigenesis, Genetic, 0302 clinical medicine, Medicine and Health Sciences, Medicine, lcsh:Science, Promoter Regions, Genetic, [SDV.BDD]Life Sciences [q-bio]/Development Biology, Endothelial Progenitor Cells, Multidisciplinary, DNA methylation, Microfilament Proteins, Gestational age, Methylation, Fetal Blood, Chromatin, Body Fluids, Nucleic acids, Blood, CpG site, 030220 oncology & carcinogenesis, Cord blood, Infant, Small for Gestational Age, Hypertension, Intercellular Signaling Peptides and Proteins, Female, Epigenetics, Anatomy, DNA modification, Infant, Premature, Chromatin modification, Maternal Age, Research Article, Chromosome biology, Adult, Cell biology, Real-Time Polymerase Chain Reaction, Andrology, 03 medical and health sciences, Vasculogenesis, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], CpG Islands, DNA Methylation, Endothelial Progenitor Cells/metabolism, Fetal Blood/metabolism, Humans, Infant, Premature/growth & development, Infant, Premature/metabolism, Infant, Small for Gestational Age/growth & development, Infant, Small for Gestational Age/metabolism, Intercellular Signaling Peptides and Proteins/genetics, Intercellular Signaling Peptides and Proteins/metabolism, Membrane Proteins/genetics, Membrane Proteins/metabolism, Sequence Analysis, DNA, Genetics, Treatment Guidelines, Health Care Policy, Biology and life sciences, business.industry, lcsh:R, Membrane Proteins, Neonates, DNA, Health Care, 030104 developmental biology, Angiomotins, lcsh:Q, Gene expression, business, Developmental Biology

    وصف الملف: application/pdf

  5. 5

    المصدر: Scopus-Elsevier
    Human Molecular Genetics, Vol. 11, No 23 (2002) pp. 2829-2836
    Human Molecular Genetics, vol. 11, no. 23, pp. 2829-2836

    مصطلحات موضوعية: Male, Epithelial sodium channel, Sodium Channels/ metabolism, Membrane Proteins/ genetics/ metabolism, DNA Mutational Analysis, RNA, Messenger/metabolism, Xenopus, Deafness, Neoplasm Proteins/ genetics/ metabolism, Endoplasmic Reticulum, Sodium Channels, Serine, Mice, Xenopus laevis, 0302 clinical medicine, Genes, Recessive/genetics, Spiral Ganglion/metabolism, Endoplasmic Reticulum/metabolism, Organ of Corti, In Situ Hybridization, Genetics (clinical), ddc:616, 0303 health sciences, Organ of Corti/metabolism, biology, Reverse Transcriptase Polymerase Chain Reaction, Serine Endopeptidases, Stria Vascularis, General Medicine, Transmembrane protein, Neoplasm Proteins, Protein Transport, medicine.anatomical_structure, DNA Primers/chemistry, Female, Rabbits, Spiral Ganglion, Proteases, Genotype, Mutation, Missense/ genetics, Blotting, Western, Mutation, Missense, Genes, Recessive, In Vitro Techniques, 03 medical and health sciences, Animals, Binding Sites, Deafness/genetics, Deafness/metabolism, Epithelial Sodium Channel, Humans, Membrane Proteins/genetics, Membrane Proteins/metabolism, Mutation, Missense/genetics, Neoplasm Proteins/genetics, Neoplasm Proteins/metabolism, Oocytes/metabolism, Rats, Serine Endopeptidases/genetics, Serine Endopeptidases/metabolism, Sodium Channels/metabolism, Stria Vascularis/metabolism, otorhinolaryngologic diseases, Genetics, medicine, RNA, Messenger, Serine Endopeptidases/ genetics/ metabolism, Epithelial Sodium Channels, Molecular Biology, DNA Primers, 030304 developmental biology, Serine protease, Endoplasmic reticulum, Membrane Proteins, biology.organism_classification, Molecular biology, Oocytes, biology.protein, Deafness/ genetics/metabolism, sense organs, 030217 neurology & neurosurgery

    وصف الملف: application/pdf

  6. 6

    المساهمون: Virology, Helmholtz Centre for infection research, Inhoffenstr. 7, 38124 Braunschweig, Germany.

    المصدر: Journal of Virology, 90(9), 4298-4307. American Society for Microbiology
    Journal of Virology, vol. 90, no. 9, pp. 4298-4307
    Journal of Virology

    وصف الملف: application/pdf

  7. 7

    المساهمون: ANS - Amsterdam Neuroscience, APH - Amsterdam Public Health, Paediatric Genetics

    المصدر: American journal of human genetics, 80(3), 550-560. Cell Press
    Pasutto, F, Sticht, H, Hammersen, G, Gillessen-Kaesbach, G, Fitzpatrick, D R, Nürnberg, G, Brasch, F, Schirmer-Zimmermann, H, Tolmie, J L, Chitayat, D, Houge, G, Fernández-Martínez, L, Keating, S, Mortier, G, Hennekam, R C M, von der Wense, A, Slavotinek, A, Meinecke, P, Bitoun, P, Becker, C, Nürnberg, P, Reis, A & Rauch, A 2007, ' Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation ', American Journal of Human Genetics, vol. 80, no. 3, pp. 550-60 . https://doi.org/10.1086/512203Test

    وصف الملف: application/pdf

  8. 8

    المساهمون: Universitat de Barcelona

    المصدر: Embo Journal, vol. 33, no. 20, pp. 2388-2407
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Recercat. Dipósit de la Recerca de Catalunya
    instname

    وصف الملف: application/pdf

  9. 9

    المصدر: The Journal of Experimental Medicine
    Journal of Experimental Medicine, vol. 192, no. 11, pp. 1677-1684

    وصف الملف: application/pdf

  10. 10

    المساهمون: University of Zurich, Stutzmann Meier, P

    المصدر: FEMS Microbiology Letters, vol. 295, no. 2, pp. 251-260

    وصف الملف: MsrS_V.pdf - application/pdf; application/pdf