Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Non-genetic heterogeneity - a mutation-independent driving force for the somatic evolution of tumoursHuang, Sui ; Brock, Amy ; Chang, HannahNature reviews. Genetics, 2009-05, Vol.10 (5), p.336-342 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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2 |
Material Type: Artigo de Congresso
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Amplificative-dissipative tunneling the problem of genetic mutationHugo Sanchez de Araujo Miled Hassan Youssef Moussa; Semana Integrada do Instituto de Física de São Carlos - SIFSC (12. 2022 São Carlos)Livro de Resumos São Carlos: Instituto de Física de São Carlos - IFSC, 2022São Carlos Instituto de Física de São Carlos - IFSC 2022Localização: IFSC - Inst. Física de São Carlos (PROD034104 )(Acessar) |
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3 |
Material Type: Artigo
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The multistep hypothesis of ALS revisited: The role of genetic mutationsChiò, Adriano ; Mazzini, Letizia ; DʼAlfonso, Sandra ; Corrado, Lucia ; Canosa, Antonio ; Moglia, Cristina ; Manera, Umberto ; Bersano, Enrica ; Brunetti, Maura ; Barberis, Marco ; Veldink, Jan H ; van den Berg, Leonard H ; Pearce, Neil ; Sproviero, William ; McLaughlin, Russell ; Vajda, Alice ; Hardiman, Orla ; Rooney, James ; Mora, Gabriele ; Calvo, Andrea ; Al-Chalabi, AmmarNeurology, 2018-08, Vol.91 (7), p.e635-e642 [Periódico revisado por pares]United States: American Academy of NeurologyTexto completo disponível |
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4 |
Material Type: Revista
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Mutation research. Genetic toxicology testingNew York, NY ElsevierAcesso online. A biblioteca também possui exemplares impressos. |
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5 |
Material Type: Artigo
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Genetic mutation analysis of hereditary spastic paraplegia: A retrospective studyCui, Fang ; Sun, LiuQing ; Qiao, Jie ; Li, JianYong ; Li, Mao ; Chen, SiYu ; Sun, Bo ; Huang, XuShengMedicine (Baltimore), 2020-06, Vol.99 (23), p.e20193 [Periódico revisado por pares]United States: Wolters Kluwer HealthTexto completo disponível |
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6 |
Material Type: Revista
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Mutation research. DNAging: genetic instability and agingAmsterdam, The Netherlands ElsevierAcesso online. A biblioteca também possui exemplares impressos. |
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7 |
Material Type: Artigo
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Developmental expression of the Sturge–Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesisWetzel-Strong, Sarah E ; Galeffi, Francesca ; Benavides, Christian ; Patrucco, Mary ; Bullock, Jessica L ; Gallione, Carol J ; Lee, Han Kyu ; Marchuk, Douglas A Bellen, HGenetics (Austin), 2023-08, Vol.224 (4) [Periódico revisado por pares]US: Oxford University PressTexto completo disponível |
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8 |
Material Type: Artigo
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Longevity effect of IGF‐1R+/− mutation depends on genetic background‐specific receptor activationXu, Jie ; Gontier, Géraldine ; Chaker, Zayna ; Lacube, Philippe ; Dupont, Joëlle ; Holzenberger, MartinAging cell, 2014-02, Vol.13 (1), p.19-28 [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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9 |
Material Type: Artigo
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Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case reportWang, Zhankui ; Wang, Xiuhua ; Liu, Baojin ; Hou, YanfengMedicine (Baltimore), 2021-03, Vol.100 (9), p.e24620-e24620 [Periódico revisado por pares]United States: Lippincott Williams & WilkinsTexto completo disponível |
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10 |
Material Type: Artigo
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Zinc deficiency or genetic mutations?—A case report of hair heterochromia in the context of MC1R genetic mutationsLei, Zhang ; Yingcai, Wan ; Jianbo, WuAustralasian journal of dermatology, 2024-05, Vol.65 (3), p.e41-e44 [Periódico revisado por pares]Australia: Wiley Subscription Services, IncTexto completo disponível |