Fuchs H - Search Results

1

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.

Simon MM, Greenaway S, White JK, Fuchs H, Gailus-Durner V, Wells S, Sorg T, Wong K, Bedu E, Cartwright EJ, Dacquin R, Djebali S, Estabel J, Graw J, Ingham NJ, Jackson IJ, Lengeling A, Mandillo S, Marvel J, Meziane H, Preitner F, Puk O, Roux M, Adams DJ, Atkins S, Ayadi A, Becker L, Blake A, Brooker D, Cater H, Champy MF, Combe R, Danecek P, di Fenza A, Gates H, Gerdin AK, Golini E, Hancock JM, Hans W, Hölter SM, Hough T, Jurdic P, Keane TM, Morgan H, Müller W, Neff F, Nicholson G, Pasche B, Roberson LA, Rozman J, Sanderson M, Santos L, Selloum M, Shannon C, Southwell A, Tocchini-Valentini GP, Vancollie VE, Westerberg H, Wurst W, Zi M, Yalcin B, Ramirez-Solis R, Steel KP, Mallon AM, de Angelis MH, Herault Y, Brown SD. Simon MM, et al. Among authors: fuchs h. Genome Biol. 2013 Jul 31;14(7):R82. doi: 10.1186/gb-2013-14-7-r82. Genome Biol. 2013. PMID: 23902802 Free PMC article.

2

An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice.

Ahituv N, Erven A, Fuchs H, Guy K, Ashery-Padan R, Williams T, de Angelis MH, Avraham KB, Steel KP. Ahituv N, et al. Among authors: fuchs h. Mamm Genome. 2004 Jun;15(6):424-32. doi: 10.1007/s00335-004-2334-z. Mamm Genome. 2004. PMID: 15181535

3

Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation.

Pau H, Hawker K, Fuchs H, De Angelis MH, Steel KP. Pau H, et al. Among authors: fuchs h. Otol Neurotol. 2004 Sep;25(5):707-13. doi: 10.1097/00129492-200409000-00010. Otol Neurotol. 2004. PMID: 15353999

4

A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.

Rhodes CR, Hertzano R, Fuchs H, Bell RE, de Angelis MH, Steel KP, Avraham KB. Rhodes CR, et al. Among authors: fuchs h. Mamm Genome. 2004 Sep;15(9):686-97. doi: 10.1007/s00335-004-2344-x. Mamm Genome. 2004. PMID: 15389316

5

Hush puppy: a new mouse mutant with pinna, ossicle, and inner ear defects.

Pau H, Fuchs H, de Angelis MH, Steel KP. Pau H, et al. Among authors: fuchs h. Laryngoscope. 2005 Jan;115(1):116-24. doi: 10.1097/01.mlg.0000150693.31130.a0. Laryngoscope. 2005. PMID: 15630379

6

Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4.

Hawker K, Fuchs H, Angelis MH, Steel KP. Hawker K, et al. Among authors: fuchs h. Int J Audiol. 2005 Mar;44(3):171-7. doi: 10.1080/14992020500057434. Int J Audiol. 2005. PMID: 15916118

7

Sex-dependent susceptibility to Listeria monocytogenes infection is mediated by differential interleukin-10 production.

Pasche B, Kalaydjiev S, Franz TJ, Kremmer E, Gailus-Durner V, Fuchs H, Hrabé de Angelis M, Lengeling A, Busch DH. Pasche B, et al. Among authors: fuchs h. Infect Immun. 2005 Sep;73(9):5952-60. doi: 10.1128/IAI.73.9.5952-5960.2005. Infect Immun. 2005. PMID: 16113316 Free PMC article.

8

Systematic, standardized and comprehensive neurological phenotyping of inbred mice strains in the German Mouse Clinic.

Schneider I, Tirsch WS, Faus-Kessler T, Becker L, Kling E, Busse RL, Bender A, Feddersen B, Tritschler J, Fuchs H, Gailus-Durner V, Englmeier KH, de Angelis MH, Klopstock T. Schneider I, et al. Among authors: fuchs h. J Neurosci Methods. 2006 Oct 15;157(1):82-90. doi: 10.1016/j.jneumeth.2006.04.002. Epub 2006 May 23. J Neurosci Methods. 2006. PMID: 16720049

9

New ENU-induced semidominant mutation, Ali18, causes inflammatory arthritis, dermatitis, and osteoporosis in the mouse.

Abe K, Fuchs H, Lisse T, Hans W, Hrabé de Angelis M. Abe K, et al. Among authors: fuchs h. Mamm Genome. 2006 Sep;17(9):915-26. doi: 10.1007/s00335-006-0014-x. Epub 2006 Sep 8. Mamm Genome. 2006. PMID: 16964445

10

The mouse Trm1-like gene is expressed in neural tissues and plays a role in motor coordination and exploratory behaviour.

Vauti F, Goller T, Beine R, Becker L, Klopstock T, Hölter SM, Wurst W, Fuchs H, Gailus-Durner V, de Angelis MH, Arnold HH. Vauti F, et al. Among authors: fuchs h. Gene. 2007 Mar 15;389(2):174-85. doi: 10.1016/j.gene.2006.11.004. Epub 2006 Nov 17. Gene. 2007. PMID: 17198746

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