Gallagher PM - Search Results

1

Functional modeling of vitamin responsiveness in yeast: a common pyridoxine-responsive cystathionine beta-synthase mutation in homocystinuria.

Kim CE, Gallagher PM, Guttormsen AB, Refsum H, Ueland PM, Ose L, Folling I, Whitehead AS, Tsai MY, Kruger WD. Kim CE, et al. Among authors: gallagher pm. Hum Mol Genet. 1997 Dec;6(13):2213-21. doi: 10.1093/hmg/6.13.2213. Hum Mol Genet. 1997. PMID: 9361025

2

Characterization of mutations in the cystathionine beta-synthase gene in Irish patients with homocystinuria.

Gallagher PM, Naughten E, Hanson NQ, Schwichtenberg K, Bignell M, Yuan M, Ward P, Yap S, Whitehead AS, Tsai MY. Gallagher PM, et al. Mol Genet Metab. 1998 Dec;65(4):298-302. doi: 10.1006/mgme.1998.2771. Mol Genet Metab. 1998. PMID: 9889017 Free article.

3

High frequency (71%) of cystathionine beta-synthase mutation G307S in Irish homocystinuria patients.

Gallagher PM, Ward P, Tan S, Naughten E, Kraus JP, Sellar GC, McConnell DJ, Graham I, Whitehead AS. Gallagher PM, et al. Hum Mutat. 1995;6(2):177-80. doi: 10.1002/humu.1380060211. Hum Mutat. 1995. PMID: 7581402 No abstract available.

4

Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?

Ramsbottom D, Scott JM, Molloy A, Weir DG, Kirke PN, Mills JL, Gallagher PM, Whitehead AS. Ramsbottom D, et al. Among authors: gallagher pm. Clin Genet. 1997 Jan;51(1):39-42. doi: 10.1111/j.1399-0004.1997.tb02412.x. Clin Genet. 1997. PMID: 9084933

5

Autosomal dominant peripheral cystic retinal patches and non-cystic retinal tufts associated with peripapillary crescents, retinal breaks and uveitis.

Cahill M, Gallagher P, Whitehead A, Acheson R. Cahill M, et al. Graefes Arch Clin Exp Ophthalmol. 2001 Feb;239(2):102-8. doi: 10.1007/s004170000239. Graefes Arch Clin Exp Ophthalmol. 2001. PMID: 11372537

6

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.

Gallagher PM, Meleady R, Shields DC, Tan KS, McMaster D, Rozen R, Evans A, Graham IM, Whitehead AS. Gallagher PM, et al. Circulation. 1996 Nov 1;94(9):2154-8. doi: 10.1161/01.cir.94.9.2154. Circulation. 1996. PMID: 8901666

7

Gene-gene interactions and neural tube defects.

Whitehead AS, Molloy AM, Ramsbottom D, Weir DG, Kirke PN, Mills JL, Gallagher PM, Scott JM. Whitehead AS, et al. Among authors: gallagher pm. Clin Genet. 1999 Feb;55(2):133-4. doi: 10.1034/j.1399-0004.1999.550213.x. Clin Genet. 1999. PMID: 10189094 No abstract available.

8

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.

Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, Weir DG, Shields DC, Scott JM. Whitehead AS, et al. QJM. 1995 Nov;88(11):763-6. QJM. 1995. PMID: 8542260

9

Olmos AA, Sterczala AJ, Parra ME, Dimmick HL, Miller JD, Deckert JA, Sontag SA, Gallagher PM, Fry AC, Herda TJ, Trevino MA. Olmos AA, et al. Among authors: gallagher pm. Acta Physiol (Oxf). 2023 Sep;239(1):e14024. doi: 10.1111/apha.14024. Epub 2023 Aug 8. Acta Physiol (Oxf). 2023. PMID: 37551144

10

Myofiber hypertrophy adaptations following 6 weeks of low-load resistance training with blood flow restriction in untrained males and females.

Reece TM, Godwin JS, Strube MJ, Ciccone AB, Stout KW, Pearson JR, Vopat BG, Gallagher PM, Roberts MD, Herda TJ. Reece TM, et al. Among authors: gallagher pm. J Appl Physiol (1985). 2023 May 1;134(5):1240-1255. doi: 10.1152/japplphysiol.00704.2022. Epub 2023 Apr 6. J Appl Physiol (1985). 2023. PMID: 37022967 Free PMC article.

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