Haldane F - Search Results

1

From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis.

Klinge L, Laval S, Keers S, Haldane F, Straub V, Barresi R, Bushby K. Klinge L, et al. Among authors: haldane f. FASEB J. 2007 Jun;21(8):1768-76. doi: 10.1096/fj.06-7659com. Epub 2007 Mar 15. FASEB J. 2007. PMID: 17363620

2

The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.

von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM. von der Hagen M, et al. Among authors: haldane f. Neuromuscul Disord. 2005 Dec;15(12):863-77. doi: 10.1016/j.nmd.2005.09.002. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288871

3

Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display.

Huang Y, Verheesen P, Roussis A, Frankhuizen W, Ginjaar I, Haldane F, Laval S, Anderson LV, Verrips T, Frants RR, de Haard H, Bushby K, den Dunnen J, van der Maarel SM. Huang Y, et al. Among authors: haldane f. Eur J Hum Genet. 2005 Jun;13(6):721-30. doi: 10.1038/sj.ejhg.5201414. Eur J Hum Genet. 2005. PMID: 15827562

4

Mitochondrial DNA deletions in human skin reflect photo- rather than chronologic aging.

Birch-Machin MA, Tindall M, Turner R, Haldane F, Rees JL. Birch-Machin MA, et al. Among authors: haldane f. J Invest Dermatol. 1998 Feb;110(2):149-52. doi: 10.1046/j.1523-1747.1998.00099.x. J Invest Dermatol. 1998. PMID: 9457910 Free article.

5

Human insulin receptor substrate-1: variant sequences in familial non-insulin-dependent diabetes mellitus.

Armstrong M, Haldane F, Taylor RW, Humphriss D, Berrish T, Stewart MW, Turnbull DM, Alberti KG, Walker M. Armstrong M, et al. Among authors: haldane f. Diabet Med. 1996 Feb;13(2):133-8. doi: 10.1002/(SICI)1096-9136(199602)13:2<133::AID-DIA7>3.0.CO;2-2. Diabet Med. 1996. PMID: 8641117

6

Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity.

Birch-Machin MA, Healy E, Turner R, Haldane F, Belgaid CE, Darlington S, Stephenson AM, Munro C, Messenger AG, Rees JL. Birch-Machin MA, et al. Among authors: haldane f. Br J Dermatol. 1997 Sep;137(3):339-43. Br J Dermatol. 1997. PMID: 9349326

7

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma.

Valverde P, Healy E, Sikkink S, Haldane F, Thody AJ, Carothers A, Jackson IJ, Rees JL. Valverde P, et al. Among authors: haldane f. Hum Mol Genet. 1996 Oct;5(10):1663-6. doi: 10.1093/hmg/5.10.1663. Hum Mol Genet. 1996. PMID: 8894704

8

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Taylor RW, Chinnery PF, Haldane F, Morris AA, Bindoff LA, Wilson J, Turnbull DM. Taylor RW, et al. Among authors: haldane f. Ann Neurol. 1996 Sep;40(3):459-62. doi: 10.1002/ana.410400318. Ann Neurol. 1996. PMID: 8797538

9

Relationship between insulin sensitivity and insulin receptor substrate-1 mutations in non-diabetic relatives of NIDDM families.

Armstrong M, Haldane F, Avery PJ, Mitcheson J, Stewart MW, Turnbull DM, Walker M. Armstrong M, et al. Among authors: haldane f. Diabet Med. 1996 Apr;13(4):341-5. doi: 10.1002/(SICI)1096-9136(199604)13:4<341::AID-DIA80>3.0.CO;2-F. Diabet Med. 1996. PMID: 9162610 Clinical Trial.

10

Identification of many crystal forms of Aspergillus nidulans dehydroquinate synthase.

Nichols CE, Ren J, Lamb H, Haldane F, Hawkins AR, Stammers DK. Nichols CE, et al. Among authors: haldane f. Acta Crystallogr D Biol Crystallogr. 2001 Feb;57(Pt 2):306-9. doi: 10.1107/s0907444900019429. Acta Crystallogr D Biol Crystallogr. 2001. PMID: 11173489

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