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16 Records found.
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1.
Bowl, M.R.* et al.: A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nat. Commun. 8:886 (2017)
2.
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
3.
Hrabě de Angelis, M. et al.: Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat. Genet. 47, 969-978 (2015)
4.
Simon, M.M.* et al.: A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 14:R82 (2013)
5.
Bosman, E.A.* ; Quint, E.* ; Fuchs, H. ; Hrabě de Angelis, M. & Steel, K.P.*: Catweasel mice: A novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome. Dev. Biol. 328, 285-296 (2009)
6.
Lewis, M.A.* et al.: An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat. Genet. 41, 614-618 (2009)
7.
Hertzano, R.* et al.: A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells. PLoS Genet. 4:e1000207 (2008)
8.
Spiden, S.L.* et al.: The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. PLoS Genet. 4:e1000238 (2008)
9.
Hawker, K.* ; Fuchs, H. ; Hrabě de Angelis, M. & Steel, K.P.*: Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4. Int. J. Audiol. 44, 171-177 (2005)
10.
Pau, H.* ; Fuchs, H. ; Hrabě de Angelis, M. & Steel, K.P.*: Hush puppy: A new mouse mutant with pinna, ossicle and inner ear defects. Laryngoscope 115, 116-124 (2005)
11.
Ahituv, N.* et al.: An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice. Mamm. Genome 15, 424-432 (2004)
12.
Pau, H.* ; Hawker, K.* ; Fuchs, H. ; Hrabě de Angelis, M. & Steel, K.P.*: Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation. Otol. Neurotol. 25, 707-713 (2004)
13.
Rhodes, C.R.* et al.: A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. Mamm. Genome 15, 686-697 (2004)
14.
Vreugde, S.* et al.: Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat. Genet. 30, 257-258 (2002)
15.
Kiernan, A.E.* et al.: The Notch ligand Jagged1 is required for inner ear sensory development. Proc. Natl. Acad. Sci. U.S.A. 98, 3873-3878 (2001)
16.
Kiernan, A.E.* et al.: Several new mouse mutations affect semicircular canal morphogenesis of the inner ear. Br. J. Audiol 34, 85-86 (2000)