يعرض 1 - 10 نتائج من 28 نتيجة بحث عن '"Chromosomes, Human, Pair 17 genetics"', وقت الاستعلام: 1.11s تنقيح النتائج
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    المساهمون: Agency for science, technology and research [Singapore] (A*STAR), Farhat Hached University Hospital, University of Basel (Unibas), Nagoya University Graduate School of Medicine, Guy's Hospital [London], The Walter and Eliza Hall Institute of Medical Research (WEHI), University of Melbourne, Graduate School of Medicine and Faculty of Medicine Kyoto University, Unité différenciation épidermique et auto-immunité rhumatoïde (UDEAR), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Pierre-Paul Riquet [Toulouse], CHU Toulouse [Toulouse], Alexandria University [Alexandrie], University of Medicine and Pharmacy 'Carol Davila' Bucharest (UMPCD), Koc University, School of Medicine, Istanbul, National University of Singapore (NUS), ACS - Amsterdam Cardiovascular Sciences, ARD - Amsterdam Reproduction and Development, Center for Reproductive Medicine, Farhat Hached University Hospital [Tunisie], Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), CARBILLET, Véronique

    المصدر: Cell
    Cell, Elsevier, 2016, 167 (1), pp.187-202.e17. ⟨10.1016/j.cell.2016.09.001⟩
    Cell, 167(1), 187-+. Cell Press
    Cell, 2016, 167 (1), pp.187-202.e17. ⟨10.1016/j.cell.2016.09.001⟩

    مصطلحات موضوعية: 0301 basic medicine, MESH: Signal Transduction, Skin Neoplasms, MESH: Keratosis / genetics, Inflammasomes, MESH: Carcinoma / genetics, MESH: Amino Acid Sequence, germline, MESH: Chromosomes, Human, Pair 17 / genetics, Pyrin domain, Germline, MSPC, [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases, MESH: Germ-Line Mutation, MESH: Skin Neoplasms / genetics, MESH: Syndrome, MESH: Adaptor Proteins Signal Transducing / chemistry, MESH: Skin Neoplasms / pathology, MESH: Adaptor Proteins, Signal Transducing / genetics, integumentary system, NLRP1, MESH: Genetic Predisposition to Disease, MESH: Epidermis / pathology, Inflammasome, MESH: Hyperplasia / genetics, Syndrome, 3. Good health, Pedigree, MESH: Pyrin / chemistry, [SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases, MESH: Protein Domains, genodermatosis, medicine.drug, Signal Transduction, keratinocytes, MESH: Hyperplasia / pathology, multiple self-healing squamous cell carcinoma, MESH: Pedigree, NLR Proteins, Biology, ASC, MESH: Apoptosis Regulatory Proteins / genetics, General Biochemistry, Genetics and Molecular Biology, MESH: Inflammasomes / genetics, 03 medical and health sciences, AIM2, Germline mutation, Protein Domains, inflammasome, skin inflammation, Paracrine Communication, medicine, Humans, cancer, Genetic Predisposition to Disease, MESH: Interleukin-1 / metabolism, Amino Acid Sequence, MESH: Paracrine Communication, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, MESH: Keratosis / pathology, Innate immune system, Hyperplasia, gain-of-function, MESH: Humans, MESH: Apoptosis Regulatory Proteins / chemistry, IL-1, Carcinoma, keratosis lichenoides chronica, Keratosis, Pyrin, medicine.disease, 030104 developmental biology, MESH: Carcinoma / pathology, Immunology, Cancer research, MSSE, Skin cancer, Epidermis, Apoptosis Regulatory Proteins, MESH: Inflammasomes / metabolism, Chromosomes, Human, Pair 17, Interleukin-1

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    وصف الملف: application/pdf

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    مورد إلكتروني

    المصدر: Journal of clinical oncology, 33 (15

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