0964-5691 < 0964-6906 < 0965-1721

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 28.
[20-40] [0 - 20][0 - 28]

Ident.	Authors (with country if any)	Title
001322 (2009)	Susan E. Swanberg ; Raman P. Nagarajan ; Sailaja Peddada ; Dag H. Yasui ; Janine M. Lasalle	Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism
001443 (2008)	Carl T. Fulp ; Ginam Cho ; Eric D. Marsh ; Ilya M. Nasrallah ; Patricia A. Labosky ; Jeffrey A. Golden	Identification of Arx transcriptional targets in the developing basal forebrain
001490 (2007)	Franois Foulquier ; Daniel Ungar ; Ellen Reynders ; Renate Zeevaert ; Philippa Mills ; Maria Teresa Garca-Silva ; Paz Briones ; Bryan Winchester ; Willy Morelle ; Monty Krieger ; Willem Annaert ; Gert Matthijs	A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1Cog8 interaction in COG complex formation
001501 (2008)	Hans Matsson ; Jacqueline Eason ; Carol S. Bookwalter ; Joakim Klar ; Peter Gustavsson ; Jan Sunnegrdh ; Henrik Enell ; Anders Jonzon ; Miikka Vikkula ; Ilse Gutierrez ; Javier Granados-Riveron ; Mark Pope ; Frances Bulock ; Jane Cox ; Thelma E. Robinson ; Feifei Song ; David J. Brook ; Steven Marston ; Kathleen M. Trybus ; Niklas Dahl	Alpha-cardiac actin mutations produce atrial septal defects
001502 (2008)	Julie Van Der Zee ; Hazel Urwin ; Sebastiaan Engelborghs ; Marc Bruyland ; Rik Vandenberghe ; Bart Dermaut ; Tim De Pooter ; Karin Peeters ; Patrick Santens ; Peter P. De Deyn ; Elizabeth M. Fisher ; John Collinge ; Adrian M. Isaacs ; Christine Van Broeckhoven	CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro
001519 (2007)	Masashi Demura ; Regina M. Martin ; Makio Shozu ; Siby Sebastian ; Kazuto Takayama ; Wei-Tong Hsu ; Roger A. Schultz ; Kirk Neely ; Michael Bryant ; Berenice B. Mendonca ; Keiichi Hanaki ; Susumu Kanzaki ; David B. Rhoads ; Madhusmita Misra ; Serdar E. Bulun	Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene
001520 (2008)	Veerle Labarque ; Kathleen Freson ; Chantal Thys ; Christine Wittevrongel ; Marc F. Hoylaerts ; Rita De Vos ; Nathalie Goemans ; Chris Van Geet	Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgery
001536 (2008)	Cynthia Shannon Weickert ; Ana L. Miranda-Angulo ; Jenny Wong ; William R. Perlman ; Sarah E. Ward ; Vakkalanka Radhakrishna ; Richard E. Straub ; Daniel R. Weinberger ; Joel E. Kleinman	Variants in the estrogen receptor alpha gene and its mRNA contribute to risk for schizophrenia

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