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Resultados de 11 a 20 de 167  para Produção Intelectual da USP

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11
Integrin signaling in inflammatory and neuropathic pain in the rat
Integrin signaling in inflammatory and neuropathic pain in the rat
Material Type:
Artigo 		Adicionar ao Meu Espaço

Integrin signaling in inflammatory and neuropathic pain in the rat

Olayinka A. Dina Carlos Amílcar Parada; Jenny Yeh; Xiaojie Chen; Gordon C McCarter; Jon D Levine

European Journal of Neuroscience Oxford v. 19, p. 634-642, 2004

Oxford 2004

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1424708 )(Acessar)

12
A review of craniofacial disorders caused by spliceosomal defects
A review of craniofacial disorders caused by spliceosomal defects
Material Type:
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A review of craniofacial disorders caused by spliceosomal defects

D. Lehallea D Wieczorek; Roseli Maria Zechi-Ceide; Maria Rita Passos-Bueno; S Lyonnet; J Amie; C.T Gordon

Clinical Genetics p. on-line

Hoboken 2015

Item não circula. Consulte sua biblioteca.(Acessar)

13
Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears
Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears

Christhofer T. Gordon Florence Petit; P Kroisel; Linda Jakobsen; Roseli Maria Zechi Ceide; Myriam Oufadem; C Bole-Feysot; Patrick Nitschke; Arnold Munnich; Stanislas Lyonnet; M Holder-Espinasse; Jeanne Amiel; European Human Genetics Conference (2014 Milan)

Abstracts Milan : ESHG, 2014

Milan ESHG 2014

Item não circula. Consulte sua biblioteca.(Acessar)

14
A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects
A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects

Eleonora Palagano Christopher T Gordon; Paolo Uva; Dario Strina; Clémantine Dimartino; Anna Villa; Jeanne Amiel; Maria Leine Guion-Almeida; Siulan Vendramini Paulovich Pittoli; Nancy Mizue Kokitsu Nakata; Roseli Maria Zechi-Ceide; Cristina Sobacchi

Bone New York v. 153, id. 116152, 7 p., Dec. 2021

New York 2021

Item não circula. Consulte sua biblioteca.(Acessar)

15
Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome
Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome

Christopher T. Gordon Christopher M Cunniff; Glenn E Green; Roseli Maria Zechi-Ceide; Jason M Johnson; Alex Henderson; Florence Petit; Nancy Mizue Kokitsu Nakata; Maria Leine Guion-Almeida; Arnold Munnich; Michael L Cunningham; Stanislas Lyonnet; Jeanne Amiel

American Journal of Medical Genetics Part A New York v. 164, n. 7, p. 1850-1853, July 2014

Ney York 2014

Acesso online

16
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears

Christopher J Gordon Florence Petit; Peter Michael Kroisel; Linda Jakobsen; Roseli Maria Zechi-Ceide; Myriam Oufadem; C Bole-Feysot; Solenn Pruvost; Cécile Masson; Frédéric Tores; Thierry Hieu; Patrick Nitschké; Pernille Lindholm; Philippe Pellerin; Maria Leine Guion-Almeida; Nancy Mizue Kokitsu Nakata; Siulan Vendramini Paulovich Pittoli; Arnold Munnich; Stanislas Lyonnet; Muriel Holder-Espinasse; Jeanne Amiel

American Journal of Human Genetics Chicago v. 93, n. 6, p. 1118-1125, Dec. 2013

Chicago 2013

Item não circula. Consulte sua biblioteca.(Acessar)

17
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia
Material Type:
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Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia

Christopher T Gordon K. Nicole Weaver; Roseli Maria Zechi-Ceide; Erik C Madsen; Andre L. P Tavares; Myriam Oufadem; Yukiko Kurihara; Igor Adameyko; Arnaud Picard; Sylvain Breton; Sébastien Pierrot; Martin Biosse-Duplan; Norine Voisin; Cécile Masson; Christine Bole-Feysot; Patrick Nitschké; Marie-Ange Delrue; Didier Lacombe; Maria Leine Guion-Almeida; Priscila Padilha Moura; Daniela Gamba Garib; Arnold Munnich; Patrik Ernfors; Robert B Hufnagel; Robert J Hopkin

American Journal of Human Genetics Chicago v. 96, n. 4, p. 519-531, Apr. 2015

Chicago 2015

Acesso online

18
Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding
Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding
Material Type:
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Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding

Vanessa Luiza Tavares Christhofer T Gordon; T Torres; N Voisin; D Bertola; Roseli Maria Zechi Ceide; T. Y Tan; A. A. C Heggie; E Propst; B. C Papsin; Nancy Mizue Kokitsu Nakata; Maria Leine Guion-Almeida; Siulan Vendramini Pailovich Pittoli; Stanislas Lyonnet; Jeanne Amiel; Maria Rita Passos-Bueno; European Human Genetics Conference (2014 Milan)

Abstracts Milan : ESHG, 2014

Milan ESHG 2014

Item não circula. Consulte sua biblioteca.(Acessar)

19
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
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Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome

Vanessa L. Romanelli Tavares Roseli M Zechi-Ceide; Debora R Bertola; Christopher T Gordon; Simone G Ferreira; Gabriella S. P Hsia; Guilherme L Yamamoto; Suzana A. M Ezquina; Nancy M Kokitsu-Nakata; Siulan Vendramini-Pittoli; Renato S Freitas; Josiane Souza; Cesar A Raposo-Amaral; Mayana Zatz; Jeanne Amiel; Maria L Guion-Almeida; Maria Rita Passos-Bueno

American Journal of Medical Genetics Part A Hoboken v.173, n.4, p.938-945, 2017

Hoboken 2017

Item não circula. Consulte sua biblioteca.(Acessar)

20
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect

Vanessa Luiza Romanelli Tavares Christopher T Gordon; Roseli Maria Zechi-Ceide; Nancy Mizue Kokitsu Nakata; Norine Voisin; Tiong Y Tan; Andrew A Heggie; Siulan Vendramini Paulovich Pittoli; Evan J Propst; Blake C Papsin; Tatiana Teixeira Torres; Henk Buermans; Luciane Portas Capelo; Johan T Den Dunnen; Maria Leine Guion-Almeida; Stanislas Lyonnet; Jeanne Amiel; Maria Rita Passos-Bueno

European Journal of Human Genetics London v. 23, n. 4, p. 481-485, Apr. 2015

London 2015

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Gordon, C
  2. Camargo, E
  3. Silva, F
  4. Meneguetti, J
  5. Gordon, A

Neste Assunto:

  1. Física
  2. Física Nuclear
  3. Acervo Museológico (Etnologia)
  4. Mutação Genética
  5. Curadoria Museológica

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

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