Henderson HE - Search Results

1

Long-distance PCR-based strategy for preparing knock-in vectors directly from ES cell genomic DNA.

Zhang LH, Henderson HE. Zhang LH, et al. Among authors: henderson he. Biotechniques. 1998 Nov;25(5):784-6, 788. doi: 10.2144/98255bm06. Biotechniques. 1998. PMID: 9821578 Free article. No abstract available.

2

Characteristics of primary biliary cirrhosis in British Columbia's First Nations population.

Arbour L, Rupps R, Field L, Ross P, Erikson A, Henderson H, Hill W, Yoshida E. Arbour L, et al. Can J Gastroenterol. 2005 May;19(5):305-10. doi: 10.1155/2005/203028. Can J Gastroenterol. 2005. PMID: 15915245

3

Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans.

Orren A, Owen EP, Henderson HE, van der Merwe L, Leisegang F, Stassen C, Potter PC. Orren A, et al. Among authors: henderson he. Clin Exp Immunol. 2012 Mar;167(3):459-71. doi: 10.1111/j.1365-2249.2011.04525.x. Clin Exp Immunol. 2012. PMID: 22288589 Free PMC article.

4

Severe hypertriglyceridaemia as a result of familial chylomicronaemia: the Cape Town experience.

Pouwels ED, Blom DJ, Firth JC, Henderson HE, Marais AD. Pouwels ED, et al. Among authors: henderson he. S Afr Med J. 2008 Feb;98(2):105-8. S Afr Med J. 2008. PMID: 18350203

5

Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family.

Parham KL, Roberts A, Thomas A, Würzner R, Henderson HE, Potter PC, Morgan BP, Orren A. Parham KL, et al. Among authors: henderson he. Mol Immunol. 2007 Apr;44(10):2756-60. doi: 10.1016/j.molimm.2006.11.022. Epub 2007 Jan 25. Mol Immunol. 2007. PMID: 17257682

6

An OTC deficiency 'phenocopy' in association with Klinefelter syndrome.

Swarts L, Leisegang F, Owen EP, Henderson HE. Swarts L, et al. Among authors: henderson he. J Inherit Metab Dis. 2007 Feb;30(1):101. doi: 10.1007/s10545-006-0489-3. Epub 2006 Dec 20. J Inherit Metab Dis. 2007. PMID: 17186414

7

Autosomal recessive hypercholesterolaemia: discrimination of ARH protein and LDLR function in the homozygous FH phenotype.

Abera AB, Marais AD, Raal FJ, Leisegang F, Jones S, George P, Henderson HE. Abera AB, et al. Among authors: henderson he. Clin Chim Acta. 2007 Mar;378(1-2):33-7. doi: 10.1016/j.cca.2006.10.005. Epub 2006 Oct 13. Clin Chim Acta. 2007. PMID: 17150201

8

Librarians collaborating with nurses.

Henderson HE, Crabtree AB, Lewis JM, Wensel LM. Henderson HE, et al. Med Ref Serv Q. 2006 Winter;25(4):55-63. doi: 10.1300/J115v25n04_06. Med Ref Serv Q. 2006. PMID: 17135152

9

X-linked hyper IgM (HIGM1) in an African kindred: the first report from South Africa.

Pienaar S, Eley BS, Hughes J, Henderson HE. Pienaar S, et al. Among authors: henderson he. BMC Pediatr. 2003 Nov 28;3:12. doi: 10.1186/1471-2431-3-12. BMC Pediatr. 2003. PMID: 14641931 Free PMC article.

10

The AGT gene in Africa: a distinctive minor allele haplotype, a polymorphism (V326I), and a novel PH1 mutation (A112D) in Black Africans.

Coulter-Mackie MB, Tung A, Henderson HE, Toone JR, Applegarth DA. Coulter-Mackie MB, et al. Among authors: henderson he. Mol Genet Metab. 2003 Jan;78(1):44-50. doi: 10.1016/s1096-7192(02)00204-4. Mol Genet Metab. 2003. PMID: 12559847

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