Stanford PM - Search Results

1

Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia.

Stanford PM, Shepherd CE, Halliday GM, Brooks WS, Schofield PW, Brodaty H, Martins RN, Kwok JB, Schofield PR. Stanford PM, et al. Brain. 2003 Apr;126(Pt 4):814-26. doi: 10.1093/brain/awg090. Brain. 2003. PMID: 12615641

2

Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies.

Stanford PM, Brooks WS, Teber ET, Hallupp M, McLean C, Halliday GM, Martins RN, Kwok JB, Schofield PR. Stanford PM, et al. J Neurol. 2004 Sep;251(9):1098-104. doi: 10.1007/s00415-004-0489-x. J Neurol. 2004. PMID: 15372253

3

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

Stanford PM, Halliday GM, Brooks WS, Kwok JB, Storey CE, Creasey H, Morris JG, Fulham MJ, Schofield PR. Stanford PM, et al. Brain. 2000 May;123 ( Pt 5):880-93. doi: 10.1093/brain/123.5.880. Brain. 2000. PMID: 10775534

4

Similar early clinical presentations in familial and non-familial frontotemporal dementia.

Piguet O, Brooks WS, Halliday GM, Schofield PR, Stanford PM, Kwok JB, Spillantini MG, Yancopoulou D, Nestor PJ, Broe GA, Hodges JR. Piguet O, et al. Among authors: stanford pm. J Neurol Neurosurg Psychiatry. 2004 Dec;75(12):1743-5. doi: 10.1136/jnnp.2003.031948. J Neurol Neurosurg Psychiatry. 2004. PMID: 15548495 Free PMC article.

5

Prolactin and the prolactin receptor: new targets of an old hormone.

Harris J, Stanford PM, Oakes SR, Ormandy CJ. Harris J, et al. Among authors: stanford pm. Ann Med. 2004;36(6):414-25. doi: 10.1080/07853890410033892. Ann Med. 2004. PMID: 15513293 Free article. Review.

6

Socs2 and elf5 mediate prolactin-induced mammary gland development.

Harris J, Stanford PM, Sutherland K, Oakes SR, Naylor MJ, Robertson FG, Blazek KD, Kazlauskas M, Hilton HN, Wittlin S, Alexander WS, Lindeman GJ, Visvader JE, Ormandy CJ. Harris J, et al. Among authors: stanford pm. Mol Endocrinol. 2006 May;20(5):1177-87. doi: 10.1210/me.2005-0473. Epub 2006 Feb 9. Mol Endocrinol. 2006. PMID: 16469767

7

KIBRA interacts with discoidin domain receptor 1 to modulate collagen-induced signalling.

Hilton HN, Stanford PM, Harris J, Oakes SR, Kaplan W, Daly RJ, Ormandy CJ. Hilton HN, et al. Among authors: stanford pm. Biochim Biophys Acta. 2008 Mar;1783(3):383-93. doi: 10.1016/j.bbamcr.2007.12.007. Epub 2008 Jan 9. Biochim Biophys Acta. 2008. PMID: 18190796 Free article.

8

A mutation in the viral sensor 2'-5'-oligoadenylate synthetase 2 causes failure of lactation.

Oakes SR, Gallego-Ortega D, Stanford PM, Junankar S, Au WWY, Kikhtyak Z, von Korff A, Sergio CM, Law AMK, Castillo LE, Allerdice SL, Young AIJ, Piggin C, Whittle B, Bertram E, Naylor MJ, Roden DL, Donovan J, Korennykh A, Goodnow CC, O'Bryan MK, Ormandy CJ. Oakes SR, et al. Among authors: stanford pm. PLoS Genet. 2017 Nov 8;13(11):e1007072. doi: 10.1371/journal.pgen.1007072. eCollection 2017 Nov. PLoS Genet. 2017. PMID: 29117179 Free PMC article.

9

Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16.

Cavanaugh JA, Callen DF, Wilson SR, Stanford PM, Sraml ME, Gorska M, Crawford J, Whitmore SA, Shlegel C, Foote S, Kohonen-Corish M, Pavli P. Cavanaugh JA, et al. Among authors: stanford pm. Ann Hum Genet. 1998 Jul;62(Pt 4):291-8. doi: 10.1046/j.1469-1809.1998.6240291.x. Ann Hum Genet. 1998. PMID: 9924607

10

Screening for MEN1 mutations in patients with atypical endocrine neoplasia.

Dackiw AP, Cote GJ, Fleming JB, Schultz PN, Stanford P, Vassilopoulou-Sellin R, Evans DB, Gagel RF, Lee JE. Dackiw AP, et al. Surgery. 1999 Dec;126(6):1097-103; discussion 1103-4. doi: 10.1067/msy.2099.101376. Surgery. 1999. PMID: 10598193

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