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Refinado por: assunto: Mutação Genética remover
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1
T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis
T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis
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T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis

Ruth J. Napier Ellen J Lee; Michael P Davey; Emily E Vance; João Marcello Fortes Furtado; Paige E Snow; Kimberly A Samson; Sydney J Lashley; Brieanna R Brown; Reiko Horai; Mary J Mattapallil; Biying Xu; Michelle C Callegan; Luke S Uebelhoer; Christina L Lancioni; Richard K Vehe; Bryce A Binstadt; Justine R Smith; Rachel R Caspi; Holly L Rosenzweig

Nature Communications London v. 11, n. 1, art. 5406, 2020

London 2020

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3016421 Acervo Digital )(Acessar)

2
A Novel Mutation of IL1RN in the Deficiency of Interleukin-1 Receptor Antagonist Syndrome
A Novel Mutation of IL1RN in the Deficiency of Interleukin-1 Receptor Antagonist Syndrome
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A Novel Mutation of IL1RN in the Deficiency of Interleukin-1 Receptor Antagonist Syndrome

Adriana A. Jesus Mazen Osman; Clovis A Silva; Peter W Kim; Tuyet-Hang Pham; Massimo Gadina; Barbara Yang; Débora R Bertola; Magda Carneiro-Sampaio; Polly J Ferguson; Blair R Renshaw; Ken Schooley; Michael Brown; Asma Al-Dosari; Jamil Al-Alami; John E Sims; Raphaela Goldbach-Mansky; Hatem El-Shanti

Arthritis & Rheumatism New York v. 63, n. 12, p. 4007-4017, 2011

New York 2011

Acesso online. A biblioteca também possui exemplares impressos.

3
A Novel Mutation of IL1RN in the Deficiency of Interleukin-1 Receptor Antagonist Syndrome
A Novel Mutation of IL1RN in the Deficiency of Interleukin-1 Receptor Antagonist Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Novel Mutation of IL1RN in the Deficiency of Interleukin-1 Receptor Antagonist Syndrome

Adriana A. Jesus Mazen Osman; Clovis A Silva; Peter W Kim; Tuyet-Hang Pham; Massimo Gadina; Barbara Yang; Débora R Bertola; Magda Carneiro-Sampaio; Polly J Ferguson; Blair R Renshaw; Ken Schooley; Michael Brown; Asma Al-Dosari; Jamil Al-Alami; John E Sims; Raphaela Goldbach-Mansky; Hatem El-Shanti

Arthritis & Rheumatism New York v. 63, n. 12, p. 4007-4017, 2011

New York 2011

Acesso online. A biblioteca também possui exemplares impressos.

4
Comparative evolutionary genetics of deleterious load in sorghum and maize
Comparative evolutionary genetics of deleterious load in sorghum and maize
Material Type:
Artigo 		Adicionar ao Meu Espaço

Comparative evolutionary genetics of deleterious load in sorghum and maize

Roberto Lozano Elodie Gazave; Jhonathan Pedroso Rigal dos Santos; Markus G Stetter; Ravi Valluru; Nonoy Bandillo; Samuel Fernandes; Patrick J Brown; Nadia Shakoor; Todd C Mockler; Elizabeth A Cooper; M Taylor Perkins; Edward S Buckler; Jeffrey Ross-Ibarra; Michael A Gore

Nature Plants Heidelberg v. 7, p. 17-24, 2021

Heidelberg 2021

Item não circula. Consulte sua biblioteca.(Acessar)

5
Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes
Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes
Material Type:
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Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes

Claudia M.B. Carvalho Shivakumar Vasanth; Marwan Shinawi; Chad Russell; Melissa B Ramocki; Chester W Brown; Jesper Graakjaer; Anne-Bine Skytte; Gayle S Patel; LaDonna Immken; Kyrieckos Aleck; Cynthia Lim; Sau Wai Cheung; Carla Rosenberg; Nicholas Katsanis; James R Lupski

American Journal of Human Genetics v. 95, p. 565-578, 2014

Cambridge 2014

Item não circula. Consulte sua biblioteca.(Acessar)

6
Ataxin-2 as potential disease modifier in C90RF72 expansion carriers
Ataxin-2 as potential disease modifier in C90RF72 expansion carriers
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Ataxin-2 as potential disease modifier in C90RF72 expansion carriers

Marka van Blitterswijk Mullen Bianca; Michael Heckman; Lea T Grinberg; Matthew Backer; Mariely de Jesus Hernandez; Patricia Brown; Melissa Murray; Ging Yuek Hsiung; Heather Stewart; Anna Karydas; Elizabeth Finger; Andrew Kertesz; Eillen Bigio; Sandra Weintraub; Marsel Mesulam; Kimmo Hatanpaa; Charles White III; Manuela Neumann; Michael Strong; Thomas Beach; Zbigniew Wszolek; Carol Lippa; Richard Caselli; Leonard Petrucelli; Keith Josephs; Joseph Parisi; David Knopman; Ronald Peterson; Ian Mackenzie Seeley, william; Bruce Miller; Kevin Boylan; Neil Graff-Radford; Bradley Boeve; Dennis Dickson; Rosa Rademarkers

Neurobiology of aging New York v. 35, n. 3, p. 2421e13-2421e17, 2014

New York 2014

Localização: FM - Fac. Medicina    (BCSEP 016 2014 )(Acessar)

7
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia
Material Type:
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TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia

Marka van Blitterswijk Bianca Mullen; Alexandra M Nicholson; Kevin F Bieniek; Michael G Heckman; Matthew C Baker; Mariely DeJesus‑Hernandez; NiCole A Finch; Patricia H Brown; Melissa E Murray; Ging‑Yuek R Hsiung; Heather Stewart; Anna M Karydas; Elizabeth Finger; Andrew Kertesz; Eileen H Bigio; Sandra Weintraub; Marsel Mesulam; Kimmo J Hatanpaa; Charles L White III; Michael J Strong; Thomas G Beach; Zbigniew K Wszolek; Carol Lippa; Richard Caselli; Leonard Petrucelli; Keith A Josephs; Joseph E Parisi; David S Knopman; Ronald C Petersen; Ian R Mackenzie; William W Seeley; Lea T Grinberg; Bruce L Miller; Kevin B Boylan; Neill R Graff‑Radford; Bradley F Boeve; Dennis W Dickson; Rosa Rademakers

Acta Neuropathologica Berlin v. 127, n. 3, p. 397-406, 2014

Berlin 2014

Localização: FM - Fac. Medicina    (BCSEP 090 2014 )(Acessar)

8
Genetic modifiers in carriers of repeat expansions in the C90RF72 gene
Genetic modifiers in carriers of repeat expansions in the C90RF72 gene
Material Type:
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Genetic modifiers in carriers of repeat expansions in the C90RF72 gene

Marka van Blitterswijk Bianca Mullen; Aleksandra Wojtas; Michael G Heckman; Nancy N Diedhi; Matthew C Baker; Mariely De Jesus-Hernandez; Patricia H Brown; Melissa E Murray; Ging-Yuek R Hsiung; Heather Stewart; Anna M Karydas; Elizabeth Finger; Andrew Kertesz; Eileen H Bigio; Sandra Weintraub; Marsel Mesulam; Kimmo J Hatanpaa; Charles L White III; Manuela Neumann; Michael J Strong; Thomas G Beach; Zbigniew Wszolek; Carol Lippa; Richard Caselli; Leonard Petrucekki; Keith Josephs; Joseph Parisi; David Knopman; Ronald Peterson; Ian Mackenzie; William Seeley; Lea Grinberg; Bruce Miller; Kevin Boylan; Neil Graff-Radford; Bradley Boeve; Dennis Dickson; Rosa Rademakers

Molecular Neurodegeneration London v. 9, p. 38, 2014

London 2014

Localização: FM - Fac. Medicina    (BCSEP 574 2014 )(Acessar)

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Deste Autor:

  1. Brown, P
  2. Stewart, H
  3. Knopman, D
  4. Beach, T
  5. Strong, M

Neste Assunto:

  1. Fenótipos
  2. Imunofenotipagem
  3. Interleucina 1 (Deficiência)
  4. Doenças Autoimunes
  5. Western Blotting

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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