Tee L - Search Results

1

Polymorphisms associated with circulating sex hormone levels in postmenopausal women.

Dunning AM, Dowsett M, Healey CS, Tee L, Luben RN, Folkerd E, Novik KL, Kelemen L, Ogata S, Pharoah PD, Easton DF, Day NE, Ponder BA. Dunning AM, et al. Among authors: tee l. J Natl Cancer Inst. 2004 Jun 16;96(12):936-45. doi: 10.1093/jnci/djh167. J Natl Cancer Inst. 2004. PMID: 15199113

2

Association of the progesterone receptor gene with breast cancer risk: a single-nucleotide polymorphism tagging approach.

Pooley KA, Healey CS, Smith PL, Pharoah PD, Thompson D, Tee L, West J, Jordan C, Easton DF, Ponder BA, Dunning AM. Pooley KA, et al. Among authors: tee l. Cancer Epidemiol Biomarkers Prev. 2006 Apr;15(4):675-82. doi: 10.1158/1055-9965.EPI-05-0679. Cancer Epidemiol Biomarkers Prev. 2006. PMID: 16614108

3

The patched polymorphism Pro1315Leu (C3944T) may modulate the association between use of oral contraceptives and breast cancer risk.

Chang-Claude J, Dunning A, Schnitzbauer U, Galmbacher P, Tee L, Wjst M, Chalmers J, Zemzoum I, Harbeck N, Pharoah PD, Hahn H. Chang-Claude J, et al. Among authors: tee l. Int J Cancer. 2003 Mar 1;103(6):779-83. doi: 10.1002/ijc.10889. Int J Cancer. 2003. PMID: 12516098 Free article.

4

Role of CHEK2*1100delC in unselected series of non-BRCA1/2 male breast cancers.

Neuhausen S, Dunning A, Steele L, Yakumo K, Hoffman M, Szabo C, Tee L, Baines C, Pharoah P, Goldgar D, Easton D. Neuhausen S, et al. Among authors: tee l. Int J Cancer. 2004 Jan 20;108(3):477-8. doi: 10.1002/ijc.11385. Int J Cancer. 2004. PMID: 14648718 Free article. No abstract available.

5

Maintenance of murine platelet homeostasis by the kinase Csk and phosphatase CD148.

Mori J, Nagy Z, Di Nunzio G, Smith CW, Geer MJ, Al Ghaithi R, van Geffen JP, Heising S, Boothman L, Tullemans BME, Correia JN, Tee L, Kuijpers MJE, Harrison P, Heemskerk JWM, Jarvis GE, Tarakhovsky A, Weiss A, Mazharian A, Senis YA. Mori J, et al. Among authors: tee l. Blood. 2018 Mar 8;131(10):1122-1144. doi: 10.1182/blood-2017-02-768077. Epub 2018 Jan 4. Blood. 2018. PMID: 29301754 Free PMC article.

6

Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome.

McKie AB, Alsaedi A, Vogt J, Stuurman KE, Weiss MM, Shakeel H, Tee L, Morgan NV, Nikkels PG, van Haaften G, Park SM, van der Smagt JJ, Bugiani M, Maher ER. McKie AB, et al. Among authors: tee l. Acta Neuropathol Commun. 2014 Dec 5;2:148. doi: 10.1186/s40478-014-0148-0. Acta Neuropathol Commun. 2014. PMID: 25476234 Free PMC article.

7

Locus heterogeneity and Knobloch syndrome.

Joyce S, Tee L, Abid A, Khaliq S, Mehdi SQ, Maher ER. Joyce S, et al. Among authors: tee l. Am J Med Genet A. 2010 Nov;152A(11):2880-1. doi: 10.1002/ajmg.a.33619. Am J Med Genet A. 2010. PMID: 20979194 No abstract available.

8

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.

Tee L, Lim DH, Dias RP, Baudement MO, Slater AA, Kirby G, Hancocks T, Stewart H, Hardy C, Macdonald F, Maher ER. Tee L, et al. Clin Epigenetics. 2013 Dec 10;5(1):23. doi: 10.1186/1868-7083-5-23. Clin Epigenetics. 2013. PMID: 24325814 Free PMC article.

9

A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver disease.

Morgan NV, Hartley JL, Setchell KD, Simpson MA, Brown R, Tee L, Kirkham S, Pasha S, Trembath RC, Maher ER, Gissen P, Kelly DA. Morgan NV, et al. Among authors: tee l. Orphanet J Rare Dis. 2013 May 16;8:74. doi: 10.1186/1750-1172-8-74. Orphanet J Rare Dis. 2013. PMID: 23679950 Free PMC article.

10

Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL.

Morgan NV, Yngvadottir B, O'Driscoll M, Clark GR, Walsh D, Martin E, Tee L, Reid E, Titheradge HL, Maher ER. Morgan NV, et al. Among authors: tee l. Brain Commun. 2021 Jan 28;3(1):fcab002. doi: 10.1093/braincomms/fcab002. eCollection 2021. Brain Commun. 2021. PMID: 33634263 Free PMC article.

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