Jennings BA - Search Results

1

The genetics of cholesteatoma study. Loss-of-function variants in an affected family.

Prinsley P, Jennings BA, Bhutta M, Swan D, Willis G, Philpott C. Prinsley P, et al. Among authors: jennings ba. Clin Otolaryngol. 2019 Sep;44(5):826-830. doi: 10.1111/coa.13365. Epub 2019 Jul 23. Clin Otolaryngol. 2019. PMID: 31099479 No abstract available.

2

Analysis of ras point mutations and human papillomavirus 16 and 18 in cervical carcinomata and their metastases.

Willis G, Jennings B, Ball RY, New NE, Gibson I. Willis G, et al. Gynecol Oncol. 1993 Jun;49(3):359-64. doi: 10.1006/gyno.1993.1140. Gynecol Oncol. 1993. PMID: 8390962

3

A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.

Willis G, Jennings BA, Goodman E, Fellows IW, Wimperis JZ. Willis G, et al. Among authors: jennings ba. Blood Cells Mol Dis. 1997 Aug;23(2):288-91. doi: 10.1006/bcmd.1997.0145. Blood Cells Mol Dis. 1997. PMID: 9410472

4

A differential PCR assay for the detection of c-erbB 2 amplification used in a prospective study of breast cancer.

Jennings BA, Hadfield JE, Worsley SD, Girling A, Willis G. Jennings BA, et al. Mol Pathol. 1997 Oct;50(5):254-6. doi: 10.1136/mp.50.5.254. Mol Pathol. 1997. PMID: 9497915 Free PMC article.

5

Incidence of liver disease in people with HFE mutations.

Willis G, Wimperis JZ, Lonsdale R, Fellows IW, Watson MA, Skipper LM, Jennings BA. Willis G, et al. Among authors: jennings ba. Gut. 2000 Mar;46(3):401-4. doi: 10.1136/gut.46.3.401. Gut. 2000. PMID: 10673304 Free PMC article.

6

Prevalence of HFE (hemochromatosis gene) mutations in unselected male patients with type 2 diabetes.

Sampson MJ, Williams T, Heyburn PJ, Greenwood RH, Temple RC, Wimperis JZ, Jennings BA, Willis GA. Sampson MJ, et al. Among authors: jennings ba. J Lab Clin Med. 2000 Feb;135(2):170-3. doi: 10.1067/mlc.2000.104464. J Lab Clin Med. 2000. PMID: 10695662

7

HFE mutations in an inflammatory arthritis population.

Willis G, Scott DG, Jennings BA, Smith K, Bukhari M, Wimperis JZ. Willis G, et al. Among authors: jennings ba. Rheumatology (Oxford). 2002 Feb;41(2):176-9. doi: 10.1093/rheumatology/41.2.176. Rheumatology (Oxford). 2002. PMID: 11886966

8

HFE mutations in the elderly.

Willis G, Wimperis JZ, Smith K, Fellows IW, Jennings BA. Willis G, et al. Among authors: jennings ba. Blood Cells Mol Dis. 2003 Sep-Oct;31(2):240-6. doi: 10.1016/s1079-9796(03)00158-x. Blood Cells Mol Dis. 2003. PMID: 12972032

9

Longevity and C282Y mutation for haemochromatosis: survival of C282Y homozygotes does not preclude screening for HFE mutations.

Willis G, Jennings BA, Wimperis JZ. Willis G, et al. Among authors: jennings ba. BMJ. 2003 Oct 25;327(7421):990-1; author reply 991. doi: 10.1136/bmj.327.7421.990-a. BMJ. 2003. PMID: 14576264 Free PMC article. No abstract available.

10

Hepatocellular carcinoma and the penetrance of HFE C282Y mutations: a cross sectional study.

Willis G, Bardsley V, Fellows IW, Lonsdale R, Wimperis JZ, Jennings BA. Willis G, et al. Among authors: jennings ba. BMC Gastroenterol. 2005 Jun 1;5:17. doi: 10.1186/1471-230X-5-17. BMC Gastroenterol. 2005. PMID: 15929796 Free PMC article.

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