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1
The High Osmolarity Glycerol Mitogen-Activated Protein Kinase regulates glucose catabolite repression in filamentous fungi
The High Osmolarity Glycerol Mitogen-Activated Protein Kinase regulates glucose catabolite repression in filamentous fungi
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The High Osmolarity Glycerol Mitogen-Activated Protein Kinase regulates glucose catabolite repression in filamentous fungi

Leandro José de Assis Lilian Pereira Silva; Li Liu; Kerstin Schmitt; Oliver Valerius; Gerhard H Braus; Laure Nicolas Annick Ries; Gustavo Henrique Goldman

PLOS Genetics San Francisco v. 16, n. 8, art. e1008996, p. 1-27, 2020

San Francisco 2020

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 3048247 Acervo Digital )(Acessar)

2
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
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Artigo 		Adicionar ao Meu Espaço

Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice

Lisenka E. L. M. Vissers Timothy C Cox; A. Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Sarquis Jehee; Débora Romeo Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony Roscioli

PLoS Genetics San Francisco v. 7, n, 9, p. e1002278, sept. 2011

San Francisco 2011

Item não circula. Consulte sua biblioteca.(Acessar)

3
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Material Type:
Artigo 		Adicionar ao Meu Espaço

Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice

Lisenka E. L. M. Vissers Timothy C Cox; A. Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Sarquis Jehee; Débora Romeo Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony Roscioli

PLoS Genetics San Francisco v. 7, n, 9, p. e1002278, sept. 2011

San Francisco 2011

Item não circula. Consulte sua biblioteca.(Acessar)

4
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

Lea K. Davis Dongomei Yu; Clare L Keenan; Eric R Gamazon; Anuar I Konkashbaev; Eske M Derks; Benjamin M Neale; Jian Yang; S. Hong Lee; Patrick Evans; Cathy L Barr; Laura Bellodi; Fortu Benarroch; Gabriel Bedova Berrio; Oscar J Bienvenu; Michael H Bloch; Rianne M Blom; Ruth D Bruun; Cathy L Budman; Beatriz Camarena; Desmond Campbell; Carolina Cappi; Julio C. Cardona Salgado; Danielle C Cath; Maria C Cavallini; Denise A Chavira; Sylvain Chouinard; David V Conti; Edwin H Cook; Vladimir Coric; Bernadette A Cullen; Dieter Deforce; Richard Delorne; Yves Dion; Christopher K Edlund; Karin Egberts; Peter Falkai; Thomas V Fernandez; Patience J Gallagher; Helena Garrido; Daniel Geller; Simon L Girard; Hans J Grabe; Marco A Grados; Benjamin D Greenberg; Varda Gross Tsur; Stephen Haddad; Gary A Heiman; Sian M. J Hemmings; Ana G Hounie; Cornelia Illmann; Joseph Jankovic; Michael A Jenike; Robert A King; Barbara Kremeyer; Roger Kurlan; Nuria Lanzagorta; Marion Leboyer; James F Leckman; Leonhard Lennerts; Chunyu Liu; Christine Lochner; Thomas L Lowe; Fabio Macciardi; James T McCracken; Lauren MacGrant; Sandra C. Mesa Restrepo; Rainald Moessner; Jubel Morgan; Heike Muller; Dennis L Murphy; Allan L Naarden; William Cornejo Ochoa; Roel A Ophoff; Lisa Osieck; Andrew J Pakstis; Michele T Pato; Carlos N Pato; John Piacentini; Christopher Pittenger; Yehuda Pollak; Scott L Rauch; Tobias J Renner; Victor I Reus; Mark A Riddle; Mary M Robertson; Roxana Romero; Maria C Rosàrio; David Rosenberg; Guy A Rouleau; Stephan Ruhrmann; Andres Ruiz Linares; Aline S Sampaio; Jack Samuels; Paul Sandor; Brooke Sheppard; Harvey S Singer; Jan H Smit; Dan J Stein; E Strengman; Jay A Tischfield; Ana V. Valencia Duarte; Homero Pinto Vallada Filho; Filip Van Nieuwerburgh; Jeremy Veenstra VanderWeele; Susanne Walitza; Ying Wang; Jens R Wendland; Herman G. M Westenberg; Yin Yao Shugart; Eurípedes Constantino Miguel; William McMahon; Michael Wagner; Humberto Nicolini; Danielle Posthuma; Gregory L Hanna; Peter Heutink; Damiaan Denys; Paul D Arnold; Ben A Oostra; Gerald Nestadt; Nelson B Freimer; David L Pauls; Naomi R Wray; S. Evelyn Stewart; Carol A Mathews; James A Knowles; Nancy J Cox; Jeremiah M Scharf

Plos genetics San Francisco v. 9, n. 10, p. e1003864, 2013

San Francisco 2013

Localização: FM - Fac. Medicina    (BCSEP 483 2013 )(Acessar)

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Deste Autor:

  1. Wiradjaja, F
  2. Janssen, I
  3. Maga, A
  4. Bertola, D
  5. Buckley, M

Neste Assunto:

  1. Craniossinostose
  2. Mutação Genética
  3. Genômica
  4. Sequenciamento Genético
  5. Proteínas Quinases

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

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