Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin–Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning

Author： Zeniou M.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.11, Iss.23, 2002-11, pp. : 2929-2940

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Deletion of the Coffin–Lowry Syndrome Gene Rsk2 in Mice is Associated With Impaired Spatial Learning and Reduced Control of Exploratory Behavior

By Poirier R.   Jacquot S.   Vaillend C.   Soutthiphong A.   Libbey M.   Davis S.   Laroche S.   Hanauer A.   Welzl H.   Lipp H.-P.   Wolfer D.  

Behavior Genetics, Vol. 37, Iss. 1, 2007-01 ,pp. : 31-50

Springer Publishing Company

Access to resources Recommend Favorite

Mouse mutants carrying deletions that remove the genes mutated in Coffin–Lowry syndrome and lactic acidosis

By Blair H.J.   Gormally E.   Uwechue I.C.   Boyd Y.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 549-555

Oxford University Press

Access to resources Recommend Favorite

Consider the neuro‐cardiac continuum of Coffin‐Lowry syndrome!

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 8, 2015-08 ,pp. : 1954-1955

John Wiley & Sons Inc

Access to resources Recommend Favorite

Recurrent Nonconvulsive Status Epilepticus in a Patient with Coffin-Lowry Syndrome

By  

Molecular Syndromology, Vol. 6, Iss. 2, 2015-05 ,pp. : 91-95

Karger

Access to resources Recommend Favorite

Structure and expression of two members of the d4 gene family in mouse

By Mertsalov Ilja B.   Kulikova Dina A.   Alimova-Kost Maria V.   Ninkina Natalia N.   Korochkin Leonid I.   Buchman Vladimir L.  

Mammalian Genome, Vol. 11, Iss. 1, 2000-01 ,pp. : 72-74

Springer Publishing Company

Access to resources Recommend Favorite