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Secretion of the amino-terminal fragment of the hedgehog protein is necessary and sufficient for hedgehog signalling in Drosophila.
Fietz MJ, Jacinto A, Taylor AM, Alexandre C, Ingham PW. Fietz MJ, et al. Curr Biol. 1995 Jun 1;5(6):643-50. doi: 10.1016/s0960-9822(95)00129-1. Curr Biol. 1995. PMID: 7552175
Quantitative effects of hedgehog and decapentaplegic activity on the patterning of the Drosophila wing.
Ingham PW, Fietz MJ. Ingham PW, et al. Among authors: fietz mj. Curr Biol. 1995 Apr 1;5(4):432-40. doi: 10.1016/s0960-9822(95)00084-4. Curr Biol. 1995. PMID: 7627558
The hedgehog gene family in Drosophila and vertebrate development.
Fietz MJ, Concordet JP, Barbosa R, Johnson R, Krauss S, McMahon AP, Tabin C, Ingham PW. Fietz MJ, et al. Dev Suppl. 1994:43-51. Dev Suppl. 1994. PMID: 7579523
Functional analysis in Drosophila indicates that the NBCCS/PTCH1 mutation G509V results in activation of smoothened through a dominant-negative mechanism.
Hime GR, Lada H, Fietz MJ, Gillies S, Passmore A, Wicking C, Wainwright BJ. Hime GR, et al. Among authors: fietz mj. Dev Dyn. 2004 Apr;229(4):780-90. doi: 10.1002/dvdy.10499. Dev Dyn. 2004. PMID: 15042702
The cDNA-deduced amino acid sequence for trichohyalin, a differentiation marker in the hair follicle, contains a 23 amino acid repeat.
Fietz MJ, Presland RB, Rogers GE. Fietz MJ, et al. J Cell Biol. 1990 Feb;110(2):427-36. doi: 10.1083/jcb.110.2.427. J Cell Biol. 1990. PMID: 2298812 Free PMC article.
Analysis of the sheep trichohyalin gene: potential structural and calcium-binding roles of trichohyalin in the hair follicle.
Fietz MJ, McLaughlan CJ, Campbell MT, Rogers GE. Fietz MJ, et al. J Cell Biol. 1993 May;121(4):855-65. doi: 10.1083/jcb.121.4.855. J Cell Biol. 1993. PMID: 7684041 Free PMC article.
Mapping of the trichohyalin gene: co-localization with the profilaggrin, involucrin, and loricrin genes.
Fietz MJ, Rogers GE, Eyre HJ, Baker E, Callen DF, Sutherland GR. Fietz MJ, et al. J Invest Dermatol. 1992 Nov;99(5):542-4. doi: 10.1111/1523-1747.ep12667301. J Invest Dermatol. 1992. PMID: 1431214
Trichohyalin and matrix proteins.
Rogers GE, Fietz MJ, Fratini A. Rogers GE, et al. Among authors: fietz mj. Ann N Y Acad Sci. 1991 Dec 26;642:64-80; discussion 80-1. Ann N Y Acad Sci. 1991. PMID: 1809119 Review. No abstract available.
Molecular analysis of genomic DNA allows rapid, and accurate, prenatal diagnosis of peroxisomal D-bifunctional protein deficiency.
Paton BC, Solly PB, Nelson PV, Pollard AN, Sharp PC, Fietz MJ. Paton BC, et al. Among authors: fietz mj. Prenat Diagn. 2002 Jan;22(1):38-41. doi: 10.1002/pd.233. Prenat Diagn. 2002. PMID: 11810648
A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy.
Licchetta L, Bisulli F, Fietz M, Valentino ML, Morbin M, Mostacci B, Oliver KL, Berkovic SF, Tinuper P. Licchetta L, et al. Among authors: fietz m. Eur J Med Genet. 2015 Oct;58(10):540-4. doi: 10.1016/j.ejmg.2015.09.002. Epub 2015 Sep 7. Eur J Med Genet. 2015. PMID: 26360874
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