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Wolfram syndrome.
Rev Endocr Metab Disord. 2003 Mar;4(1):53-9. doi: 10.1023/a:1021875403463.
Rev Endocr Metab Disord. 2003.
PMID: 12618560
Review.
No abstract available.
Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature.
Iyer S, Korada M, Rainbow L, Kirk J, Brown RM, Shaw N, Barrett TG.
Iyer S, et al.
Acta Paediatr. 2004 Sep;93(9):1195-201.
Acta Paediatr. 2004.
PMID: 15384883
Review.
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Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM.
Rainbow LA, et al.
Clin Endocrinol (Oxf). 2005 Feb;62(2):163-8. doi: 10.1111/j.1365-2265.2004.02189.x.
Clin Endocrinol (Oxf). 2005.
PMID: 15670191
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Refining the pH response in Aspergillus nidulans: a modulatory triad involving PacX, a novel zinc binuclear cluster protein.
Bussink HJ, Bignell EM, Múnera-Huertas T, Lucena-Agell D, Scazzocchio C, Espeso EA, Bertuzzi M, Rudnicka J, Negrete-Urtasun S, Peñas-Parilla MM, Rainbow L, Peñalva MÁ, Arst HN Jr, Tilburn J.
Bussink HJ, et al.
Mol Microbiol. 2015 Dec;98(6):1051-72. doi: 10.1111/mmi.13173. Epub 2015 Oct 16.
Mol Microbiol. 2015.
PMID: 26303777
Free PMC article.
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Activation of the Aspergillus PacC zinc finger transcription factor requires two proteolytic steps.
Díez E, Alvaro J, Espeso EA, Rainbow L, Suárez T, Tilburn J, Arst HN Jr, Peñalva MA.
Díez E, et al.
EMBO J. 2002 Mar 15;21(6):1350-9. doi: 10.1093/emboj/21.6.1350.
EMBO J. 2002.
PMID: 11889040
Free PMC article.
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YPXL/I is a protein interaction motif recognized by aspergillus PalA and its human homologue, AIP1/Alix.
Vincent O, Rainbow L, Tilburn J, Arst HN Jr, Peñalva MA.
Vincent O, et al.
Mol Cell Biol. 2003 Mar;23(5):1647-55. doi: 10.1128/MCB.23.5.1647-1655.2003.
Mol Cell Biol. 2003.
PMID: 12588984
Free PMC article.
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On how a transcription factor can avoid its proteolytic activation in the absence of signal transduction.
Espeso EA, Roncal T, Díez E, Rainbow L, Bignell E, Alvaro J, Suárez T, Denison SH, Tilburn J, Arst HN Jr, Peñalva MA.
Espeso EA, et al.
EMBO J. 2000 Feb 15;19(4):719-28. doi: 10.1093/emboj/19.4.719.
EMBO J. 2000.
PMID: 10675341
Free PMC article.
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Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.
Senée V, Vattem KM, Delépine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC, Julier C.
Senée V, et al. Among authors: rainbow la.
Diabetes. 2004 Jul;53(7):1876-83. doi: 10.2337/diabetes.53.7.1876.
Diabetes. 2004.
PMID: 15220213
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