Schmahl W - Search Results

1

Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice.

Helwig U, Imai K, Schmahl W, Thomas BE, Varnum DS, Nadeau JH, Balling R. Helwig U, et al. Among authors: schmahl w. Nat Genet. 1995 Sep;11(1):60-3. doi: 10.1038/ng0995-60. Nat Genet. 1995. PMID: 7550316

2

Pax genes and skeletal development.

Balling R, Helwig U, Nadeau J, Neubüser A, Schmahl W, Imai K. Balling R, et al. Among authors: schmahl w. Ann N Y Acad Sci. 1996 Jun 8;785:27-33. doi: 10.1111/j.1749-6632.1996.tb56240.x. Ann N Y Acad Sci. 1996. PMID: 8702151 Review. No abstract available.

3

Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes.

Favor J, Bradley A, Conte N, Janik D, Pretsch W, Reitmeir P, Rosemann M, Schmahl W, Wienberg J, Zaus I. Favor J, et al. Among authors: schmahl w. Genetics. 2009 Aug;182(4):1077-88. doi: 10.1534/genetics.109.104562. Epub 2009 May 27. Genetics. 2009. PMID: 19474196 Free PMC article.

4

A non-functioning vitamin D receptor predisposes to leukaemoid reactions in mice.

Erben RG, Zeitz U, Weber K, Stierstorfer B, Wolf G, Schmahl W, Balling R, Quintanilla-Martinez L. Erben RG, et al. Among authors: schmahl w. Hematol Oncol. 2010 Dec;28(4):185-91. doi: 10.1002/hon.938. Hematol Oncol. 2010. PMID: 20301229

5

Molecular characterization of Pax6(2Neu) through Pax6(10Neu): an extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus.

Favor J, Peters H, Hermann T, Schmahl W, Chatterjee B, Neuhäuser-Klaus A, Sandulache R. Favor J, et al. Among authors: schmahl w. Genetics. 2001 Dec;159(4):1689-700. doi: 10.1093/genetics/159.4.1689. Genetics. 2001. PMID: 11779807 Free PMC article.

6

Type IV procollagen missense mutations associated with defects of the eye, vascular stability, the brain, kidney function and embryonic or postnatal viability in the mouse, Mus musculus: an extension of the Col4a1 allelic series and the identification of the first two Col4a2 mutant alleles.

Favor J, Gloeckner CJ, Janik D, Klempt M, Neuhäuser-Klaus A, Pretsch W, Schmahl W, Quintanilla-Fend L. Favor J, et al. Among authors: schmahl w. Genetics. 2007 Feb;175(2):725-36. doi: 10.1534/genetics.106.064733. Epub 2006 Dec 18. Genetics. 2007. PMID: 17179069 Free PMC article.

7

Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus.

Schmahl W, Knoedlseder M, Favor J, Davidson D. Schmahl W, et al. Acta Neuropathol. 1993;86(2):126-35. doi: 10.1007/BF00334879. Acta Neuropathol. 1993. PMID: 8213068

8

Mutagenic and teratogenic effects of acrylamide in the mammalian spot test.

Neuhäuser-Klaus A, Schmahl W. Neuhäuser-Klaus A, et al. Among authors: schmahl w. Mutat Res. 1989 Jul;226(3):157-62. doi: 10.1016/0165-7992(89)90013-4. Mutat Res. 1989. PMID: 2747730 No abstract available.

9

Diaplacental induction by ethylnitrosourea of tumours at the pial border of the central nervous system in (T X HT)F1 mice.

Schmahl W, Luz A, Leierseder-Bauer M, Neuhäuser-Klaus A. Schmahl W, et al. Carcinogenesis. 1990 Aug;11(8):1313-22. doi: 10.1093/carcin/11.8.1313. Carcinogenesis. 1990. PMID: 2387017

10

Neuropathological findings in brains of Bavarian cattle clinically suspected of bovine spongiform encephalopathy.

Miyashita M, Stierstorfer B, Schmahl W. Miyashita M, et al. Among authors: schmahl w. J Vet Med B Infect Dis Vet Public Health. 2004 Jun;51(5):209-15. doi: 10.1111/j.1439-0450.2004.00755.x. J Vet Med B Infect Dis Vet Public Health. 2004. PMID: 15330979

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