Cullen LM - Search Results

1

Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.

Crawford DH, Jazwinska EC, Cullen LM, Powell LW. Crawford DH, et al. Among authors: cullen lm. Gastroenterology. 1998 May;114(5):1003-8. doi: 10.1016/s0016-5085(98)70320-8. Gastroenterology. 1998. PMID: 9558290

2

Isolation and characterisation of cosmids to intervals within a 4.5Mb region at 6p21.3.

Jazwinska EC, Cullen LM, Zournazi A, Burt MJ, Van Der Griend B, Goldwurm S, Little PF. Jazwinska EC, et al. Among authors: cullen lm. DNA Seq. 1997;8(3):147-50. doi: 10.3109/10425179709034065. DNA Seq. 1997. PMID: 10668959

3

Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins.

Whitfield JB, Cullen LM, Jazwinska EC, Powell LW, Heath AC, Zhu G, Duffy DL, Martin NG. Whitfield JB, et al. Among authors: cullen lm. Am J Hum Genet. 2000 Apr;66(4):1246-58. doi: 10.1086/302862. Epub 2000 Mar 15. Am J Hum Genet. 2000. PMID: 10739755 Free PMC article.

4

Genetics of hemochromatosis.

Cullen LM, Anderson GJ, Ramm GA, Jazwinska EC, Powell LW. Cullen LM, et al. Annu Rev Med. 1999;50:87-98. doi: 10.1146/annurev.med.50.1.87. Annu Rev Med. 1999. PMID: 10073265 Review.

5

The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populations.

Cullen LM, Gao X, Easteal S, Jazwinska EC. Cullen LM, et al. Am J Hum Genet. 1998 Jun;62(6):1403-7. doi: 10.1086/301878. Am J Hum Genet. 1998. PMID: 9585606 Free PMC article.

6

Generation of a transcription map distal to HLA-F.

Goldwurm S, Van der Griend BF, Banyer JL, Cullen LM, Zournazi A, Menzies ML, Busfield F, Little PF, Jazwinska EC. Goldwurm S, et al. Among authors: cullen lm. Eur J Hum Genet. 1998 Sep-Oct;6(5):475-86. doi: 10.1038/sj.ejhg.5200211. Eur J Hum Genet. 1998. PMID: 9801872

7

Haemochromatosis and HLA-H.

Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP. Jazwinska EC, et al. Among authors: cullen lm. Nat Genet. 1996 Nov;14(3):249-51. doi: 10.1038/ng1196-249. Nat Genet. 1996. PMID: 8896549 No abstract available.

8

Neonatal screening for the hemochromatosis defect.

Cullen LM, Summerville L, Glassick TV, Crawford DH, Powell LW, Jazwinska EC. Cullen LM, et al. Blood. 1997 Nov 15;90(10):4236-7. Blood. 1997. PMID: 9354699 No abstract available.

9

Localization, expression and genomic structure of the gene encoding the human serine protease testisin.

Hooper JD, Bowen N, Marshall H, Cullen LM, Sood R, Daniels R, Stuttgen MA, Normyle JF, Higgs DR, Kastner DL, Ogbourne SM, Pera MF, Jazwinska EC, Antalis TM. Hooper JD, et al. Among authors: cullen lm. Biochim Biophys Acta. 2000 Jun 21;1492(1):63-71. doi: 10.1016/s0167-4781(00)00071-3. Biochim Biophys Acta. 2000. PMID: 11004480

10

Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.

Howard CM, Davies GE, Farrer MJ, Cullen LM, Coleman MM, Williamson R, Wyse RK, Palmer R, Kessling AM. Howard CM, et al. Among authors: cullen lm. Am J Hum Genet. 1993 Aug;53(2):462-71. Am J Hum Genet. 1993. PMID: 8101041 Free PMC article.

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