Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation

Expression of nucleocytoplasmic transport machinery: Clues to regulation of spermatogenic development

(2011) Andrew T. Major et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Karyopherins in nuclear transport of homeodomain proteins during development

(2011) Wenduo Ye et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Importin Alpha2-Interacting Proteins with Nuclear Roles During Mammalian Spermatogenesis1

(2011) Jennifer D. Ly-Huynh et al.   BIOLOGY OF REPRODUCTION

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

(2011) F. Kortum et al.   JOURNAL OF MEDICAL GENETICS

Genetic and Biologic Classification of Infantile Spasms

(2011) Alex R. Paciorkowski et al.   PEDIATRIC NEUROLOGY

KPNA7, an oocyte- and embryo-specific karyopherin�?�subtype, is required for porcine embryo development

(2011) Xin Wang et al.   REPRODUCTION FERTILITY AND DEVELOPMENT

Molecular basis for specificity of nuclear import and prediction of nuclear localization

(2010) Mary Marfori et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Karyopherin alpha7 (KPNA7), a divergent member of the importin alpha family of nuclear import receptors

(2010) Joshua B Kelley et al.   BMC CELL BIOLOGY

Novel Importin-α Family Member Kpna7 Is Required for Normal Fertility and Fecundity in the Mouse

(2010) Jianjun Hu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Role of Importin Alpha8, a New Member of the Importin Alpha Family of Nuclear Transport Proteins, in Early Embryonic Development in Cattle1

(2009) Jyothsna Tejomurtula et al.   BIOLOGY OF REPRODUCTION

The Roles of Multiple Importins for Nuclear Import of Murine Aristaless-related Homeobox Protein

(2009) Wenbo Lin et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

(2009) N. Le Meur et al.   JOURNAL OF MEDICAL GENETICS

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

(2009) Kimberly A Aldinger et al.   NATURE GENETICS

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

(2008) Francesca Ariani et al.   AMERICAN JOURNAL OF HUMAN GENETICS