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)
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)
Genomic and molecular landscape of DNA damage repair deficiency across the cancer genome atlas
Theo A. Knijnenburg Linghua Wang; Michael T Zimmermann; Nyasha Chambwe; Galen F Gao; Andrew D Cherniack; Huihui Fan; Hui Shen; Gregory P Way; Casey S Greene; Yuexin Liu; Rehan Akbani; Bin Feng; Lawrence A Donehower; Chase Miller; Yang Shen; Mostafa Karimi; Haoran Chen; Pora Kim; Peilin Jia; Eve Shinbrot; Shaojun Zhang; Jianfang Liu; Hai Hu; Matthew H Bailey; Christina Yau; Denise M Wolf; Zhongming Zhao; John N Weinstein; Lei Li; Li Ding; Gordon B Mills; Peter W Laird; David A Wheeler; Ilya Shmulevich; Raymond J Monnat Junior; Yonghong Xiao; Chen Wang; Houtan Noushmehr; Carlos Gilberto Carlotti Júnior; José Sebastião dos Santos; Rafael Kemp; Ajith Kumar Sankarankuty; Daniela Pretti da Cunha Tirapelli; The Cancer Genome Atlas Research Network
Cell Reports Cambridge v. 23, n. 1, p. 239-254, 2018
Cambridge 2018
Localização:
FMRP - Fac. Medicina de Ribeirão Preto
(pcd 2938364 Estantes Deslizantes )(Acessar)
Neonatal apneic phenotype in a murine congenital central hypoventilation syndrome model is induced through non‐cell autonomous developmental mechanisms
Diego Alzate-Correa Jillian Mei-Ling Liu; Mikayla Jones; Talita M Silva; Michele Joana Alves; Elizabeth Burke; Jessica Zuñiga; Behiye Kaya; Giuliana Zaza; Mehmet Tahir Aslan; Jessica Blacburn; Marina Y Shimada; Silvio A Fernandes-Junior; Kristin I Stanford; Lisa A Baer; Amber Kempton; Sakima Smith; Caroline C Szujewski; Abby Silbaugh; Jean-Charles Viemari; Alfredo J Garcia; Catherine M Czeisle; José Javier Otero; Ana Carolina Takakura; Thiago dos Santos Moreira
Brain Pathology Hoboken v. 31, n.1, p. 84-102, 2021
Hoboken Wiley-Blackwell Publishing, Inc. 2021
Item não circula. Consulte sua biblioteca.(Acessar)