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Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.

Jagger D, Collin G, Kelly J, Towers E, Nevill G, Longo-Guess C, Benson J, Halsey K, Dolan D, Marshall J, Naggert J, Forge A.

Hum Mol Genet. 2011 Feb 1;20(3):466-81. doi: 10.1093/hmg/ddq493. Epub 2010 Nov 11.


A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence.

Li G, Vega R, Nelms K, Gekakis N, Goodnow C, McNamara P, Wu H, Hong NA, Glynne R.

PLoS Genet. 2007 Jan 5;3(1):e8. Epub 2006 Nov 30.


Hedgehog signaling regulates prosensory cell properties during the basal-to-apical wave of hair cell differentiation in the mammalian cochlea.

Tateya T, Imayoshi I, Tateya I, Hamaguchi K, Torii H, Ito J, Kageyama R.

Development. 2013 Sep;140(18):3848-57. doi: 10.1242/dev.095398. Epub 2013 Aug 14.


Postnatal refinement of auditory hair cell planar polarity deficits occurs in the absence of Vangl2.

Copley CO, Duncan JS, Liu C, Cheng H, Deans MR.

J Neurosci. 2013 Aug 28;33(35):14001-16. doi: 10.1523/JNEUROSCI.1307-13.2013.


Assessing PCP in the cochlea of mammalian ciliopathy models.

Jagger DJ, Forge A.

Methods Mol Biol. 2012;839:239-48. doi: 10.1007/978-1-61779-510-7_19.


Histopathology of the human inner ear in Alström's syndrome.

Nadol JB Jr, Marshall JD, Bronson RT.

Audiol Neurootol. 2015;20(4):267-72. doi: 10.1159/000381935. Epub 2015 Jun 24.


The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway.

Collin GB, Marshall JD, King BL, Milan G, Maffei P, Jagger DJ, Naggert JK.

PLoS One. 2012;7(5):e37925. doi: 10.1371/journal.pone.0037925. Epub 2012 May 31.


Alms1-disrupted mice recapitulate human Alström syndrome.

Collin GB, Cyr E, Bronson R, Marshall JD, Gifford EJ, Hicks W, Murray SA, Zheng QY, Smith RS, Nishina PM, Naggert JK.

Hum Mol Genet. 2005 Aug 15;14(16):2323-33. Epub 2005 Jul 6.


Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

Chen J, Ingham N, Kelly J, Jadeja S, Goulding D, Pass J, Mahajan VB, Tsang SH, Nijnik A, Jackson IJ, White JK, Forge A, Jagger D, Steel KP.

PLoS Genet. 2014 Oct 30;10(10):e1004688. doi: 10.1371/journal.pgen.1004688. eCollection 2014 Oct.


Morphometry of the chinchilla organ of Corti and stria vascularis.

Santi PA, Muchow DC.

J Histochem Cytochem. 1979 Nov;27(11):1539-42.


Progressive deafness and altered cochlear innervation in knock-out mice lacking prosaposin.

Akil O, Chang J, Hiel H, Kong JH, Yi E, Glowatzki E, Lustig LR.

J Neurosci. 2006 Dec 13;26(50):13076-88.


Results of an ultrastructural study comparing stria vascularis with organ of Corti in guinea pigs treated with kanamycin.

Gratacap B, Charachon R, Stoebner P.

Acta Otolaryngol. 1985 Mar-Apr;99(3-4):339-42.


Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731.

Knorz VJ, Spalluto C, Lessard M, Purvis TL, Adigun FF, Collin GB, Hanley NA, Wilson DI, Hearn T.

Mol Biol Cell. 2010 Nov 1;21(21):3617-29. doi: 10.1091/mbc.E10-03-0246. Epub 2010 Sep 15.


Differentiation of the lateral compartment of the cochlea requires a temporally restricted FGF20 signal.

Huh SH, Jones J, Warchol ME, Ornitz DM.

PLoS Biol. 2012 Jan;10(1):e1001231. doi: 10.1371/journal.pbio.1001231. Epub 2012 Jan 3.


Scanning and transmission electron microscope studies on the organ of Corti and stria vascularis in human fetal cochlear ducts.

Fujimoto S, Yamamoto K, Hayabuchi I, Yoshizuka M.

Arch Histol Jpn. 1981 Jul;44(3):223-35.


Aging outer hair cells (OHCs) in the Fischer 344 rat cochlea: function and morphology.

Chen GD, Li M, Tanaka C, Bielefeld EC, Hu BH, Kermany MH, Salvi R, Henderson D.

Hear Res. 2009 Feb;248(1-2):39-47. doi: 10.1016/j.heares.2008.11.010. Epub 2008 Dec 10.


Cooperative functions of Hes/Hey genes in auditory hair cell and supporting cell development.

Tateya T, Imayoshi I, Tateya I, Ito J, Kageyama R.

Dev Biol. 2011 Apr 15;352(2):329-40. doi: 10.1016/j.ydbio.2011.01.038. Epub 2011 Feb 16.


GLUT4 defects in adipose tissue are early signs of metabolic alterations in Alms1GT/GT, a mouse model for obesity and insulin resistance.

Favaretto F, Milan G, Collin GB, Marshall JD, Stasi F, Maffei P, Vettor R, Naggert JK.

PLoS One. 2014 Oct 9;9(10):e109540. doi: 10.1371/journal.pone.0109540. eCollection 2014.


Kif3a regulates planar polarization of auditory hair cells through both ciliary and non-ciliary mechanisms.

Sipe CW, Lu X.

Development. 2011 Aug;138(16):3441-9. doi: 10.1242/dev.065961. Epub 2011 Jul 13.


Cockayne syndrome group B (Csb) and group a (Csa) deficiencies predispose to hearing loss and cochlear hair cell degeneration in mice.

Nagtegaal AP, Rainey RN, van der Pluijm I, Brandt RM, van der Horst GT, Borst JG, Segil N.

J Neurosci. 2015 Mar 11;35(10):4280-6. doi: 10.1523/JNEUROSCI.5063-14.2015.

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