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Publications: Research using IKMC products

2012

January 2012 A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain.

2011

December 2011 Eye development genes and known syndromes.
December 2011 Disruption of a ciliary B9 protein complex causes Meckel syndrome.
November 2011 Targeting pannexin1 improves seizure outcome.
November 2011 Two non-vesicular ATP release pathways in the mouse erythrocyte membrane.
September 2011 Rho signaling regulates pannexin 1-mediated ATP release from airway epithelia.
August 2011 TRIP8b splice forms act in concert to regulate the localization and expression of HCN1 channels in CA1 pyramidal neurons.
August 2011 Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.
July 2011 Distinct functions of kainate receptors in the brain are determined by the auxiliary subunit Neto1.
July 2011 The PPCD1 mouse: characterization of a mouse model for posterior polymorphous corneal dystrophy and identification of a candidate gene. (ERRATUM: personal communication)
July 2011 A conditional knockout resource for the genome-wide study of mouse gene function.
July 2011 Mammalian BTBD12 (SLX4) Protects against Genomic Instability during Mammalian Spermatogenesis.
June 2011 Aspartoacylase-LacZ Knockin Mice: An Engineered Model of Canavan Disease.
May 2011 SPLUNC1 Promotes Lung Innate Defense Against Mycoplasma pneumoniae Infection in Mice.
April 2011 Obligate role for ketone body oxidation in neonatal metabolic homeostasis.
February 2011 Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia.
February 2011 DLC2 modulates angiogenic responses in vascular endothelial cells by regulating cell attachment and migration.
February 2011 Semaphorin 4C and 4G are ligands of Plexin-B2 required in cerebellar development.
January 2011 Distinct modes of inhibition by sclerostin on bone morphogenetic protein and Wnt signaling pathways.

2010

November 2010 Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin.
September 2010 The PPCD1 mouse: characterization of a mouse model for posterior polymorphous corneal dystrophy and identification of a candidate gene.

2009

June 2009 Agouti C57BL/6N embryonic stem cells for mouse genetic resources.