183 related articles for article (PubMed ID: 11099667)
21. Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.
Ho MF; Monaco AP; Blonden LA; van Ommen GJ; Affara NA; Ferguson-Smith MA; Lehrach H
Am J Hum Genet; 1992 Feb; 50(2):317-30. PubMed ID: 1734714
[TBL] [Abstract][Full Text] [Related]
22. The Kell blood group system: Kell and XK membrane proteins.
Lee S; Russo D; Redman CM
Semin Hematol; 2000 Apr; 37(2):113-21. PubMed ID: 10791880
[TBL] [Abstract][Full Text] [Related]
23. Kell phenotypes in 15 Japanese patients with chronic granulomatous disease.
Ito K; Mukumoto Y; Konishi H; Sakura N; Usui T
Vox Sang; 1979; 37(1):39-40. PubMed ID: 494579
[TBL] [Abstract][Full Text] [Related]
24. Haematological changes associated with the McLeod phenotype of the Kell blood group system.
Wimer BM; Marsh WL; Taswell HF; Galey WR
Br J Haematol; 1977 Jun; 36(2):219-24. PubMed ID: 871435
[TBL] [Abstract][Full Text] [Related]
25. Chronic granulomatous disease and the Mcleod phenotype. Successful treatment of infection with granulocyte transfusions resulting in subsequent hemolytic transfusion reaction.
Brzica SM; Pineda AA; Taswell HF; Rhodes KH
Mayo Clin Proc; 1977 Mar; 52(3):153-6. PubMed ID: 839862
[TBL] [Abstract][Full Text] [Related]
26. Localization of the McLeod locus (XK) within Xp21 by deletion analysis.
Bertelson CJ; Pogo AO; Chaudhuri A; Marsh WL; Redman CM; Banerjee D; Symmans WA; Simon T; Frey D; Kunkel LM
Am J Hum Genet; 1988 May; 42(5):703-11. PubMed ID: 3358422
[TBL] [Abstract][Full Text] [Related]
27. Auto analyzer determination of red cell Kell phenotypes in patients with chronic granulomatous disease (CGD) and heterozygous carriers.
Bowell PJ; Hill FG
Br J Haematol; 1978 Jul; 39(3):351-5. PubMed ID: 698113
[TBL] [Abstract][Full Text] [Related]
28. Kell and XK immunohistochemistry in McLeod myopathy.
Jung HH; Russo D; Redman C; Brandner S
Muscle Nerve; 2001 Oct; 24(10):1346-51. PubMed ID: 11562915
[TBL] [Abstract][Full Text] [Related]
29. Elevated serum creatine phosphokinase in subjects with McLeod syndrome.
Marsh WL; Marsh NJ; Moore A; Symmans WA; Johnson CL; Redman CM
Vox Sang; 1981; 40(6):403-11. PubMed ID: 7197431
[TBL] [Abstract][Full Text] [Related]
30. Chronic Granulomatous Disease with the McLeod Phenotype: a French National Retrospective Case Series.
Lhomme F; Peyrard T; Babinet J; Abou-Chahla W; Durieu I; Moshous D; Neven B; Rohrlich PS; Albinni S; Amiranoff D; Dumont MD; Lortholary O; Héritier S; Marguet C; Suarez F; Fischer A; Blanche S; Hermine O; Mahlaoui N
J Clin Immunol; 2020 Jul; 40(5):752-762. PubMed ID: 32562208
[TBL] [Abstract][Full Text] [Related]
31. A murine monoclonal antibody against Kx protein which reacts also with beta-spectrin.
Carbonnet F; Blanchard D; Hattab C; Cochet S; Petit-Leroux Y; Loirat MJ; Cartron JP; Bertrand O
Transfus Med; 2000 Jun; 10(2):145-54. PubMed ID: 10849386
[TBL] [Abstract][Full Text] [Related]
32. The first example of the McLeod phenotype in a Japanese baby with chronic granulomatous disease.
Uchida K; Nakajima K; Shima H; Ichiba K
Transfusion; 1992 Sep; 32(7):691. PubMed ID: 1519335
[No Abstract] [Full Text] [Related]
33. Human granulocytes lack red cell Kx antigen.
Branch DR; Gaidulis L; Lazar GS
Br J Haematol; 1986 Apr; 62(4):747-55. PubMed ID: 3516199
[TBL] [Abstract][Full Text] [Related]
34. The first example of autoanti-Kx.
Sullivan CM; Kline WE; Rabin BI; Johnson CL; Marsh WL
Transfusion; 1987; 27(4):322-4. PubMed ID: 2440157
[TBL] [Abstract][Full Text] [Related]
35. [Chronic granulomatous disease and McLeod phenotype. Description of a case].
Saggese G; Baroncelli GI; Bertelloni S; Gualtieri M; Carlotti C; Cinquanta L
Minerva Pediatr; 1990 Apr; 42(4):151-6. PubMed ID: 2377152
[TBL] [Abstract][Full Text] [Related]
36. An individual with McLeod syndrome and the Kell blood group antigen K(K1).
Marsh WL; Schnipper EF; Johnson CL; Mueller KA; Schwartz SA
Transfusion; 1983; 23(4):336-8. PubMed ID: 6879675
[TBL] [Abstract][Full Text] [Related]
37. Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus.
Frey D; Mächler M; Seger R; Schmid W; Orkin SH
Blood; 1988 Jan; 71(1):252-5. PubMed ID: 3334897
[TBL] [Abstract][Full Text] [Related]
38. Unmasking of Kx antigen by reduction of disulphide bonds on normal and McLeod red cells.
Branch DR; Sy Siok Hian AL; Petz LD
Br J Haematol; 1985 Mar; 59(3):505-12. PubMed ID: 2578808
[TBL] [Abstract][Full Text] [Related]
39. McLeod syndrome resulting from a novel XK mutation.
Singleton BK; Green CA; Renaud S; Fuhr P; Poole J; Daniels GL
Br J Haematol; 2003 Aug; 122(4):682-5. PubMed ID: 12899725
[TBL] [Abstract][Full Text] [Related]
40. Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases.
Peng J; Redman CM; Wu X; Song X; Walker RH; Westhoff CM; Lee S
Gene; 2007 May; 392(1-2):142-50. PubMed ID: 17300882
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
