Watt JM - Search Results

1

McLeod neuroacanthocytosis: genotype and phenotype.

Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker RH, Daniels G, Monaco AP. Danek A, et al. Among authors: watt jm. Ann Neurol. 2001 Dec;50(6):755-64. doi: 10.1002/ana.10035. Ann Neurol. 2001. PMID: 11761473

2

Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes.

Avent ND, Liu W, Jones JW, Scott ML, Voak D, Pisacka M, Watt J, Fletcher A. Avent ND, et al. Blood. 1997 Mar 1;89(5):1779-86. Blood. 1997. PMID: 9057663 Free article.

3

FPTT is a low-incidence Rh antigen associated with a "new" partial Rh D phenotype, DFR.

Lomas C, Grässmann W, Ford D, Watt J, Gooch A, Jones J, Beolet M, Stern D, Wallace M, Tippett P. Lomas C, et al. Transfusion. 1994 Jul;34(7):612-6. doi: 10.1046/j.1537-2995.1994.34794330017.x. Transfusion. 1994. PMID: 7519797

4

Report on group 5 monoclonal antibodies (anti-glycoconjugates without AB).

Fletcher A, Watt J. Fletcher A, et al. Rev Fr Transfus Immunohematol. 1987 Dec;30(5):627-32. doi: 10.1016/s0338-4535(87)80127-7. Rev Fr Transfus Immunohematol. 1987. PMID: 3452902 No abstract available.

5

Molecular basis for Lewis alpha(1,3/1,4)-fucosyltransferase gene deficiency (FUT3) found in Lewis-negative Indonesian pedigrees.

Mollicone R, Reguigne I, Kelly RJ, Fletcher A, Watt J, Chatfield S, Aziz A, Cameron HS, Weston BW, Lowe JB. Mollicone R, et al. J Biol Chem. 1994 Aug 19;269(33):20987-94. J Biol Chem. 1994. PMID: 8063716 Free article.

6

A new low-frequency red cell antigen, 'SARAH'.

Stern DA, Hawksworth DN, Watt JM, Ford DS. Stern DA, et al. Among authors: watt jm. Vox Sang. 1994;67(1):64-7. doi: 10.1111/j.1423-0410.1994.tb05040.x. Vox Sang. 1994. PMID: 7975455

7

Assessment of clinical significance of anti-Ge in an untransfused man.

Pearson HA, Richards VL, Wylie BR, Bruce D, Watt JM, Wilkie D, Kronenberg H. Pearson HA, et al. Among authors: watt jm. Transfusion. 1991 Mar-Apr;31(3):257-9. doi: 10.1046/j.1537-2995.1991.31391165177.x. Transfusion. 1991. PMID: 2003326

8

A novel cis-AB variant allele arising from a nucleotide substitution A796C in the B transferase gene.

Mifsud NA, Watt JM, Condon JA, Haddad AP, Sparrow RL. Mifsud NA, et al. Among authors: watt jm. Transfusion. 2000 Oct;40(10):1276-7. doi: 10.1046/j.1537-2995.2000.40101276.x. Transfusion. 2000. PMID: 11061869 No abstract available.

9

Significance of anti-LU8 in pregnancy.

Watt J, Jones ML, Rose P, Pepper R. Watt J, et al. Vox Sang. 1995;68(2):130-1. doi: 10.1111/j.1423-0410.1995.tb02565.x. Vox Sang. 1995. PMID: 7762219

10

Does hybridoma technology still have a place in transfusion medicine?

Yuan FF, Watt JM, Geczy AF. Yuan FF, et al. Among authors: watt jm. Transfus Med Rev. 2002 Jul;16(3):230-8. doi: 10.1053/tmrv.2002.33436. Transfus Med Rev. 2002. PMID: 12075560 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

90 results

Search Page

Filters