Walker AP - Search Results

1

Demonstration of the presence of the "deleted" MIR122 gene in HepG2 cells.

Hamad IA, Fei Y, Kalea AZ, Yin D, Smith AJ, Palmen J, Humphries SE, Talmud PJ, Walker AP. Hamad IA, et al. Among authors: walker ap. PLoS One. 2015 Mar 26;10(3):e0122471. doi: 10.1371/journal.pone.0122471. eCollection 2015. PLoS One. 2015. PMID: 25811611 Free PMC article.

2

Double trouble: T2DM genetic risk factors play a causal role in CAD.

Hamad IA, Beaney KE, Buxton JL, Walker AP. Hamad IA, et al. Among authors: walker ap. Atherosclerosis. 2015 Aug;241(2):766-8. doi: 10.1016/j.atherosclerosis.2015.03.033. Epub 2015 Mar 25. Atherosclerosis. 2015. PMID: 25863776 No abstract available.

3

Raised serum ferritin concentration in hereditary hyperferritinemia cataract syndrome is not a marker for iron overload.

Yin D, Kulhalli V, Walker AP. Yin D, et al. Among authors: walker ap. Hepatology. 2014 Mar;59(3):1204-6. doi: 10.1002/hep.26681. Epub 2014 Jan 27. Hepatology. 2014. PMID: 24003015 Free PMC article.

4

Hepatic iron concentration, fibrosis and response to venesection associated with the A77D and V162del "loss of function" mutations in ferroportin disease.

Lim FL, Dooley JS, Roques AW, Grellier L, Dhillon AP, Walker AP. Lim FL, et al. Among authors: walker ap. Blood Cells Mol Dis. 2008 May-Jun;40(3):328-33. doi: 10.1016/j.bcmd.2007.11.001. Epub 2007 Dec 21. Blood Cells Mol Dis. 2008. PMID: 18160317

5

Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3).

Devalia V, Carter K, Walker AP, Perkins SJ, Worwood M, May A, Dooley JS. Devalia V, et al. Among authors: walker ap. Blood. 2002 Jul 15;100(2):695-7. doi: 10.1182/blood-2001-11-0132. Blood. 2002. PMID: 12091367 Free article.

6

Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.

Wallace DF, Walker AP, Pietrangelo A, Clare M, Bomford AB, Dixon JL, Powell LW, Subramaniam VN, Dooley JS. Wallace DF, et al. Among authors: walker ap. J Hepatol. 2002 Apr;36(4):474-9. doi: 10.1016/s0168-8278(01)00304-x. J Hepatol. 2002. PMID: 11943417

7

Atypical haemochromatosis: phenotypic spectrum and beta2-microglobulin candidate gene analysis.

Walker AP, Wallace DF, Partridge J, Bomford AB, Dooley JS. Walker AP, et al. J Med Genet. 1999 Jul;36(7):537-41. J Med Genet. 1999. PMID: 10424814 Free PMC article.

8

Racial and Socioeconomic Status among a Patient Population Presenting with Aneurysmal Subarachnoid Hemorrhage versus Unruptured Intracranial Aneurysm: A Single-Center Study.

Hackett AM, Adereti CO, Walker AP, Nico E, Scherschinski L, Rhodenhiser EG, Eberle AT, Naik A, Giraldo JP, Hartke JN, Rahmani R, Winkler EA, Catapano JS, Lawton MT. Hackett AM, et al. Among authors: walker ap. Brain Sci. 2024 Apr 18;14(4):394. doi: 10.3390/brainsci14040394. Brain Sci. 2024. PMID: 38672043 Free PMC article.

9

Increased leaf area index and efficiency drive enhanced production under elevated atmospheric [CO₂ ] in a pine-dominated stand showing no progressive nitrogen limitation.

Palmroth S, Kim D, Maier CA, Medvigy D, Walker AP, Oren R. Palmroth S, et al. Among authors: walker ap. Glob Chang Biol. 2024 Feb;30(2):e17190. doi: 10.1111/gcb.17190. Glob Chang Biol. 2024. PMID: 38403855

10

Risk Prediction Models for Hospital Mortality in General Medical Patients: A Systematic Review.

Hydoub YM, Walker AP, Kirchoff RW, Alzu'bi HM, Chipi PY, Gerberi DJ, Burton MC, Murad MH, Dugani SB. Hydoub YM, et al. Among authors: walker ap. Am J Med Open. 2023 Dec;10:100044. doi: 10.1016/j.ajmo.2023.100044. Epub 2023 Jun 5. Am J Med Open. 2023. PMID: 38090393 Free PMC article.

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