Heyworth PG - Search Results

1

Primary immunodeficiency mutation databases.

Vihinen M, Arredondo-Vega FX, Casanova JL, Etzioni A, Giliani S, Hammarström L, Hershfield MS, Heyworth PG, Hsu AP, Lähdesmäki A, Lappalainen I, Notarangelo LD, Puck JM, Reith W, Roos D, Schumacher RF, Schwarz K, Vezzoni P, Villa A, Väliaho J, Smith CI. Vihinen M, et al. Among authors: heyworth pg. Adv Genet. 2001;43:103-88. doi: 10.1016/s0065-2660(01)43005-7. Adv Genet. 2001. PMID: 11037300 Review.

2

Hematologically important mutations: X-linked chronic granulomatous disease (second update).

Heyworth PG, Curnutte JT, Rae J, Noack D, Roos D, van Koppen E, Cross AR. Heyworth PG, et al. Blood Cells Mol Dis. 2001 Jan-Feb;27(1):16-26. doi: 10.1006/bcmd.2000.0347. Blood Cells Mol Dis. 2001. PMID: 11162142 No abstract available.

3

Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection.

Heyworth PG, Noack D, Cross AR. Heyworth PG, et al. Blood. 2002 Sep 1;100(5):1845-51. doi: 10.1182/blood-2002-03-0861. Blood. 2002. PMID: 12176908 Free article.

4

Chronic granulomatous disease.

Heyworth PG, Cross AR, Curnutte JT. Heyworth PG, et al. Curr Opin Immunol. 2003 Oct;15(5):578-84. doi: 10.1016/s0952-7915(03)00109-2. Curr Opin Immunol. 2003. PMID: 14499268 Review.

5

A variant X-linked chronic granulomatous disease patient (X91+) with partially functional cytochrome b.

Cross AR, Heyworth PG, Rae J, Curnutte JT. Cross AR, et al. Among authors: heyworth pg. J Biol Chem. 1995 Apr 7;270(14):8194-200. doi: 10.1074/jbc.270.14.8194. J Biol Chem. 1995. PMID: 7713925 Free article.

6

Protein phosphorylation in neutrophils from patients with p67-phox-deficient chronic granulomatous disease.

Heyworth PG, Ding J, Erickson RW, Lu DJ, Curnutte JT, Badwey JA. Heyworth PG, et al. Blood. 1996 May 15;87(10):4404-10. Blood. 1996. PMID: 8639802 Free article.

7

Hematologically important mutations: X-linked chronic granulomatous disease.

Cross AR, Curnutte JT, Rae J, Heyworth PG. Cross AR, et al. Among authors: heyworth pg. Blood Cells Mol Dis. 1996;22(1):90-5. doi: 10.1006/bcmd.1996.0013. Blood Cells Mol Dis. 1996. PMID: 8807090 No abstract available.

8

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease.

Cross AR, Curnutte JT, Heyworth PG. Cross AR, et al. Among authors: heyworth pg. Blood Cells Mol Dis. 1996;22(3):268-70. doi: 10.1006/bcmd.1996.0109. Blood Cells Mol Dis. 1996. PMID: 9075578 No abstract available.

9

Hematologically important mutations: X-linked chronic granulomatous disease--an update.

Heyworth PG, Curnutte JT, Noack D, Cross AR. Heyworth PG, et al. Blood Cells Mol Dis. 1997 Dec;23(3):443-50. doi: 10.1006/bcmd.1997.0163. Blood Cells Mol Dis. 1997. PMID: 9454688 No abstract available.

10

A novel mutation in the CYBB gene resulting in an unexpected pattern of exon skipping and chronic granulomatous disease.

Noack D, Heyworth PG, Curnutte JT, Rae J, Cross AR. Noack D, et al. Among authors: heyworth pg. Biochim Biophys Acta. 1999 Aug 30;1454(3):270-4. doi: 10.1016/s0925-4439(99)00044-7. Biochim Biophys Acta. 1999. PMID: 10452961 Free article.

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