Материал: Донсков С.И., Мороков В.А. Группы крови человека. Руководство по иммуносерологии

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419.Legler T.J, Wiemann V., Koehler M. et al. Genetic variations of the D Va-category-phenotype in japanese families // Transfusion. – 1998. – V. 38 (Suppl.). – Р. 63S, S231.

420.LeglerT.J.,MaasJ.H.,BlaschkeV.etal.RHDgenotypinginweakDphenotypesbymultiple polymerase chain reactions // Transfusion. – 1998. – V. 38. – P. 434–440.

421.LemeshevY.H.,LavrovskayaE.,HuffR.,HarrisonC.Perinatalcomplicationduetoanti-Ce: acasediscussionandsuggestionfornewlaboratoryprotocol//Transfusion.–2003.–V.43. (Suppl.). – P. 96A, SP185.

422.LePennec P.Y., Rouger P., Klein M. et al. A serologic study of red cells and sera from 18 Rh:32,–46 (R N / R N persons) // Transfusion. – 1989. – V. 29. – P. 798–802.

423.Levan A., Nichols W.W., Hall B. et al. Mixture of Rh positive and Rh negative erythrocytes and chromosomal abnormalities in a case of polycythemia // Hereditas. – 1964. – V. 52. –

P.89–105.

424.Levine P. The pathogenesis of fetal erythroblastosis // N. Y. J. Med. – 1942. – V. 42. –

P.1928.

425.LevineP.,BurnhamL.,KatzinE.M.,VogelP.Theroleofisoimmunizationinthepathogenesis of erythroblastosis fetalis //Amer. J. Obstet. Gynec. – 1941. – V. 42. – P. 925–937.

426.Levine P., Celano M.The question of D (RhO), antigenic sites on human spermatozoa //Vox Sang. – 1961. – V. 6. – P. 720–723.

427.Levine P., Celano M., Falkowski F. et al.Asecond example of  −  −  −/ −  −  − or Rhnull Blood

//Transfusion. – Philad, 1965. – V. 5. – P. 492–500.

428.Levine P., Celano M., Falkowski F. et al.Asecond example of  −  −  −/ −  −  − blood, or Rhnull

//Nature. – Lond., 1964. – V. 204. – Р. 892.

429.Levine P., Celano M., McGee R. et al. D u and gene interaction in a family study. P. H. Andresen Festskrift, Munksgaard. – Copenhagen, 1957. – P. 144–145.

430.Levine P., Katzin E.M., Burnham L. Immunization in pregnancy, its possible bearing on the etiology of erythroblastosis fetalis // J.AMA. – 1941. – V. 116. – P. 825–827.

431.Levine P., Rosenfield R.E. The first example of the Rh phenotype r Gr G // Amer. J. Hum. Genet. – 1961. – V. 13. – P. 299–305.

432.Levine P., Stetson R.E. An unusual case of intragroup agglutination // J. AMA. – 1939. –

V.113. – P. 126–127.

433.Levine P., Vogel P., Katzin E.M., Burnham L. Pathogenesis of erythroblastosis fetalis: statistical evidence // Science. – 1941. – V. 94. – P. 371–372.

434.Levine P., Whithe J., Stroup M. et al. Haemolytic disease of the newborn probably due to anti-f // Nature. – Lond., 1960. – V. 185. – P. 188–189.

435.Lewis M., Anstee D.J., Brid G.W.G. et al. Blood group terminology // Vox Sang. – 1990. –

V.58. – P. 152–169.

436.Lewis M., Chown B., Kaita H. et al. Blood group antigen Go a and the Rh system // Transfusion. – 1967. – V. 7. – P. 440–441.

437.Lewis M., Kaita H., Allderdice P. et al.Assignment of the red cell antigen Targett (rh40) to the Rh blood group system //Amer. J. Hum. Genet. – 1979. –V. 31. – P. 630–633.

438.Lewis M., Kaita H., Chown B. The inheritance of the Rh blood groups. I. Frequencies in 1000 unrelated Caucasian families consisting of 2000 parents and 2806 children // Vox Sang. – 1971. – V. 20. – P. 500–508.

439.Lewis M., Macpherson C.R., Gayton J. The Rh complex R1 wo (CD we) // Can. J. Genet. Cytol. – 1965. – V. 7. – Р. 259–261.

440.Leyshon W.C. The Rh gene complex cD– segregating in a negro family // Vox Sang. – 1967. – V. 13. – P. 354–356.

441.Lighten A.D., Overton T.G., Sepulveda W. et al.Accuracy of prenatal determination of RhD type status by polymerase chain reaction with amniotic cells // Amer. J. Obstet. Gynec. – 1995. – V. 173. – P. 1182–1185.

326

442.LillevangS.,GeorgsenJ.,KristensenT.Anantibodyscreeningtestbasedontheantiglobulin gel technique, pooled test cells, and plasma // Vox Sang. – 1994. – V. 66. – P. 210–215.

443.Liu W., Jones J.W., Scott M.L. et al. Molecular analysis of two D– variantas, DHMi and DHMii // BBTS Newsietter. – 1996. – V. 21. – Аbstract.

444.Lomas C., Bruce M., Watt A. et al. Tar + individuals with anti-D: a new category DVII (Abstract) // Transfusion. – 1986. – V. 26. – Р. 560.

445.Lomas C., Grässmann W., Ford D. et al. FPTT is a low-incidence Rh antigen associated with a «new» partial Rh D phenotype, DFR // Transfusion. – 1994. – V. 34. – P. 612–616.

446.Lomas C., McColl K., Tippett P.A. Further complexities of the Rh antigen D disclosed by testing category D II cells with monoclonal anti-D // Transfus. Med. – 1993. – V. 3. –

P.67–69.

447.Lomas C., Poole J., Salaru N. et al. A low-incidence red cell antigen JAL associated with two unusual Rh gene complexes // Vox Sang. – 1990. – V. 59. – P. 39–43.

448.Lovett D.A., Crawford M.N. Js b and Go a screening of negro donors //Transfusion, Philad. – 1967. – V. 7. – Р. 442.

449.Löw B.Apractical method using Papain and incomplete Rh-antibodies in routine Rh blood grouping // Vox Sang. – 1955. – V. 5. – N 3. – Р. 94.

450.Lowe A.D., Green S.M., Voak D. et al.Ahuman-human monoclonal anti-D by direct fusion with a lymphoblastoid cell line // Vox Sang. – 1986. – V. 51. – P. 212–216.

451.Lubenko A., Contreras M., Portugal C.L. et al. Severe haemolytic disease in an infant born to an Rh(null) proposita // Vox Sang. – 1992. – V. 63. – N 1. – P. 43–47.

452.Maaskant-van Wijk P.A., Faas B.H.W., de Ruijter J.A.M. et al. Genotyping of RHD by multiplex polymerase chain reaction analysis of RHD-specific exons // Transfusion. – 1998. – V. 38. – P. 1015–1021.

453.MacGeoch C., Mitchell C.J., Carritt B. et al. Assignment of the chromosomal locus of the human 30-kDal Rh (Rhesus) blood group-antigen-related protein (Rh30) to chromosome region 1p36.13→p34 // Cytogenet. Cell Genet. – 1992. – V. 59. – P. 261–263.

454.Macpherson C.R., Stevenson T.D., Gayton J. Anti-D in a D-positive man, with positive direct Coombs test and normal red cell survival // Amer. J. Clin Path. – 1966. – V. 45. –

P.748–750.

455.Majsky A. Rychla metoda urceni Rh // Rozhledy v chir. – 1959. – V. 8. – Р. 560.

456.Majsky A., Kulhanek V. Neue Modifikation des Serum-Bromelintestes: ZweiphasenBromelintest // Z. ges. Innere Med. – 1965. – V. 20. – N 3. – Р. 93.

457.Makinodan T., Macris N.T.The effect of ficin on the agglutination of human red blood cells // J. Immunol. – 1955. – V. 75. – N 3. – Р. 192.

458.Mallinson G., Anstee D.J., Avent N.D. et al. Murine monoclonal antibody MB-2D10 recognizes Rh-related glycoproteins in the human red cell membrane // Transfusion. – 1990. – V. 30. – P. 222–225.

459.Mannoni P., Bracq C., Yvart J., Salmon C. Anomalie de fonctionnement du locus Rh au cours d’une myelofibrose // Nouv. Rev. Franc. Hemat. – 1970. – V. 10. – P. 381–388.

460.Marais I., Moores P., Smart E., Martell R. STEM, a new low-frequency Rh antigen associated with the e-variant phenotypes hr s– (rh: –18, –19) and hr B– (Rh: –31, –34) // Transfus. Med. – 1993. – V. 3. – P. 35–41.

461.Marini A.M., Matassii G., Raynal V. et al. The human rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast // Nat. Genet. – 2000. –V. 26. –

P.341–344.

462.Marsh W.L., Chaganti R.S.K., Gardner F.H. et al. Mapping human autosomes: evidence supporting the assignment of Rhesus to the short arm of chromosome No. 1 // Science. – 1974. – V. 183. – P. 966–968.

463.Masouredis S., Dupuy M., Elliot M. Relationship between Rho(D) zygosity and red cell Rho(D) antigen content in family members // J. Clin. Invest. – 1967. – V. 46. – P. 681–694.

327

464.Masouredis S.P., Sudora E.J., Mahan L., Victoria E.J. Antigen site densities and ultrastructural distribution pattems of red cell Rh antigens // Transfusion. – 1976. – V. 16. –

P.94–106.

465.Matte C. Determination automatique des groupes sanguins. Realisation d’un appareillage experimental // Rev. Franc. Transfus. – 1969. – V. 12. – Р. 213.

466.Matte C. Un laveur rapide d’hematies pour test a l’antiglobuline sur Groupamatic // Rev. Franc. Transfus. Immunohemat. – 1978. – V. 21. – N 2. – P. 479–484.

467.Matthes M. Ueber gesteigerten Blutabbau nach Transfusionen, hervorgerufen durch den blockierendenAntikörperd(anti-Hr0)//Schweiz.Med.Wschr.–1950.–V.80.–P.358–360.

468.Mazumdar P.M.H.Agglutination of normoblasts with anti-D //Vox Sang. – 1966. –V. 11. –

P.90–98.

469.McCreary J., MacIlroy M., Courtenay D.G., Ohmart D.L. The second example of antiBe a causing hemolytic disease of the newborn // Transfusion, Philad. – 1973. – V. 13. –

P.428–431.

470.McGeeR.,LevineP.,CelanoM.Firstexampleofgenotyper yr y –afamilystudy//Science.– 1957. – V. 125. – Р. 1043.

471.McGinniss M.H., Kaplan H.S., Bowen A.B., Schmidt P.J. Agglutinins for ‘null’ red blood cells // Transfusion, Philad. – 1969. – V. 9. – P. 40–42.

472.McGinnissM.H.,SchmidtP.J.,PerryM.Auto-agglutininsto‘null’redbloodcells//Abstract 26-thAABB Meeting. – Bal Harbour, 1973. – Р. 114.

473.McNeil C., Helmick W., Ferrari A. A preliminary investigation into automatic blood grouping // Vox Sang. – 1963. – V. 8. – Р. 235.

474.McNeil C., Trentelman E.F. Detection of anti-Rh antibodies by Polyvinilpirrolidone (PVP) //Amer. J. Clin. Path. – 1953. – V. 22. – N 1. – Р. 77.

475.MetaxasM.N.,Metaxas-BühlerM.AnRhgenecomplexwhichproducesweakcantigensin a mother and her son // Vox Sang. – 1961. – V. 6. – P. 136–141.

476.Mollison P.L., Engelfriet P., Contreras M. Blood Transfusion in Clinical Medicine. –10-th ed. – Oxford: BSP, 1997. – 1033 p.

477.Moore B.Antibody detection and identification by autoanalyzer haemagglutination system // Haematologia. – 1981. – V. 14. – N 3. – P. 265–276.

478.Moore B., Fernandes L. Reappraisal of an autoanalyser haemagglutination system for anti-D quantitation // Scand. J. Haemat. – 1971. – V. 9. – Р. 492.

479.Moore B., Greenwood M., Newstead P.H., Miller G.W. Rh typing using bro­melin and incomplete antisera // Biblioth. Haemat. – 1962. – V. 13. – Р. 233.

480.Moore B., McIntyre J., Brown F., Read H.C. Recognition of the rare Rh chromosome D −  − // Canad. med.Ass. J. – 1960. – V. 82. – P. 187–191.

481.Moore S., Green C. The identification of specific Rhesus-polypeptide-blood-group-ABH- active-glycoprotein complexes in the human red-cell membrane // Biochem. J. – 1987. –

V.244. – P. 735–741.

482.Moore S., Woodrow C., McClelland D. Isolation of membrane components associated with human red cell antigens Rh(D), (c), (E) and Fy2 // Nature. – 1982. – V. 295. – P. 529–531.

483.Moore S., Woodrow C.F., McClelland D.B.L. Isolation of membrane components associated withhumanredcellantigensRh(D),(c),(E),andFy a //Nature.–1982.–V.295.–P.529–531.

484.Moores P. Rh18 and hr S blood groups and antibodies // Vox Sang. – 1994. – V. 66. –

P.225–230.

485.Moores P.P. An Asiatic blood group chimera. Paper read at Blood Trans: Congr. – Port Elizabeth, 1966.

486.Moor-Jankovski J., Wiener A.S., Rogers C.M. Human blood group factors in non-human primates // Nature. – 1964. – V. 202. – P. 663–665.

487.Moor-Jankovski J., Wiener A.S., Socha W.W. et al. Blood-group homologues in orangutans and gorillas of the human Rh-Hr and the chimpanzee C-E-F-systems // Fol. Primat. – 1973. – V. 19. – P. 360–367.

328

488.Morganti D. Su und nuova, facile, rapida e sicura tecnica per la determinatione in serie del tipo Rh (Papain slide test) // Minerva nipol. – 1958. – V. 8. – N 6. – Р. 188.

489.Morton J.A., Pickles M.M. The proteolytic enzyme test for detecting incomplete antibodies

//J. Clin. Path. – 1951. – V. 4. – Р. 189.

490.Morton J.A., Pickles M.M. Use of trypsin in the detection of incomplete anti-Rh antibodies

//Nature. – 1947. – V. 159. – Р. 779.

491.Mota M., Fonseca N.L., Rodrigues A. et al.Anti-D alloimmunization by weak D type 1 red bloodcellswithaverylowantigendensity//VoxSang.–2005.–V.88.–N2.–P.130–135.

492.Moulds J. Rhnull: amorphs and regulators // AABB Meeting: Seminar on Recent Advances in Immunohematology – Bal Harbour, 1973.

493.Moulds J. et al // Transfusion. – 1980. – V. 20. – Р. 631 (Abstract)

494.Mourant A.E.Anew Rhesus antibody // Nature. – 1945. – V. 155. – Р. 542.

495.Mourant A.E., Ikin E.W., Hässing A. et al. Uber das Vorkommen des Rhesusgens E u in einer Ostschweizer Familie // Schweiz. Med. Wschr. – 1952. – V. 82. – Р. 1100 (6 pages in reprint).

496.Mouro I., Colin Y., Cherif-Zahar B. et al. Molecular genetic basis of the human Rhesus blood group system // Nat. Genet. – 1993. – V. 5. – P. 62–65.

497.Mouro I., Colin Y., Sistonen P. et al. Molecular basis of the RhC W (Rh8) and RhC x (Rh9) blood group specificities // Blood. – 1995. – V. 86. – P. 1196–1201.

498.Mouro I., Le Van Kim C., van Rhenen D.J. et al. Rearrangements of the blood group RhD geneassociatedwiththeD-VIcategoryphenotype//Blood.–1994.–V.83.–P.1129–1135.

499.Murray J. Albumin antibodies for Rh Grouping (Letter to the editor) // Brit. Med. J. – 1951. – V. 11. – Р. 118.

500.Murray J., Clark E.C. Production of anti-Rh in guinea pigs from human erythrocytes // Nature. – Lond., 1952. – V. 169. – P. 886–887.

501.Nagel V., Kneiphoff H., Pekker St. et al. Unexplained appearance of antibody in an Rhnull donor // Vox Sang. – 1972. – V. 22. – P. 519–523.

502.Nakajima H., Misawa S., Ota K.Afurther example of D −  −/D −  − (R0R0) found among the Japanese // Proc. Jap.Acad. – 1965. – V. 41. – P. 488–492.

503.Narayanan S., Orton S., Leparc G. et al. Ultraviolet and visible light spectrophotometric approachtobloodtyping:objectiveanalysisbyagglutinationindex//Transfusion.–1999.– V. 39. – P. 1051–1059.

504.Nash R., ShojaniaA.M. Hematological aspect of Rh deficiency syndrome: a case report and

a review of the literature //Am. J. Hematol. – 1987. – V. 24. – P. 267–276.

505. Nevaulinna H., Pircola A. General aspects of antibody screening of blood donors and significance of automated techniques of Groupamatic // Rev. Frans. Transfus. Immunohemat. – 1978. – V. 21. – N 2. – P. 419–420.

506.Nicholas J.W., Jenkins W.J., Marsh W.L. Human blood chimeras.Astudy of surviving twins

//Brit med. J. – V. I. – Р. 1458–1460.

507.Nijenhuis L.E. Comments on the genetical structure of the Rhesus system // Vox Sang. – 1961. – V. 6. – P. 229–232.

508.Noizat-Pirenne F., Lee K., Le Pennec P. et al. Rare RHCE phenotypes in black individuals ofAfro-Caribbean origin: identification and transfusion safety // Blood. – 2002. – V. 100. – Р. 4223–4231.

509.Noizat-Pirenne F., Mouro I., Le Pennec P. et al. To new alleles of the RHCE gene in Black individuals: the Rhce allele ceMO and RhcE allele cEMI // Brit. J. Haemat. – 2001. –

V.113. – P. 672–679.

510.Northoff H., Goldmann S.F., Lattke H., Steinbach P. A patient, mosaic for Rh and Fy antigens lacking other signs of chimerism or chromosomal disorder // Vox Sang. – 1984. –

V.47. – N 2. – Р.164–169.

329

511.Okubo Y., Yamaduchi H., Tomita T., Nagao N. A D variant, D el? // Transfusion­. – 1984. –

V.24. – Р. 542.

512.Okuda H., Kawano M., Iwamoto S. et al. The RHD gene is highly detectable in RhDnegative Japanese donors // J. Clin. Invest. – 1997. – V. 100. – P. 373–379.

513.Omi T., Takahashi J., Seno T. et al. Isolation, characterization, and family study of DTI, a novel partial D phenotype affecting the fourth external loop of D polypeptides // Transfusion. – 2002. – V. 42. – N 4. – P. 481–489.

514.O’Reilly R.A., Lombard C.M., Azzi R.L. Delayed hemolytic transfusion reaction associated withRhantibodyanti-f:firstreportedcase//VoxSang.–1985.–V.49.–N5.–P.336–339.

515.O’Riordan J.P., Wilkinson J.L., Huth M.C. et al. The Rh gene complex cdE u // Vox Sang. – 1962. – V. 7. – P. 14–21.

516.O’Shea K.P., Oyen R., Sausais L. et al. A MAR-like antibody in a DCWe / DCWe person // Transfusion. – 2001. – V. 41. – N 1. – P. 53–55.

517.Paradis G., Bazin R., Lemieux R. Protective effect of the membrane skeleton on the immunologic reactivity of the human red cell Rho(D) antigen // J. Immunol. – 1986. –

V.137. – P. 240–244.

518.Peoples J., DuCross M., McQuiston D. et al. Automated blood typing. The auto Typer: a new instrument for the hospital blood bank.Advances in automated analysis, Mediad, 1 nc, White Plains. – N.Y., 1970. – V. 1. – Р. 265.

519.Pereira C., Sobrinho-Simoes M., Araujo F. Genotyping RHD zygosity using real-time polymerase chain reaction // Vox Sang. – 2003. – V. 84. – N 3. – Р. 243.

520.Pfeiffer R.A. Unpublished observations. Цит. по Race R.R., Sanger R. Blood Groups in Man. – 6-th ed. – Oxford: BSP, 1975. – 659 p.

521.Phillips P., Voak D. Can pooled red cells be used for antibody screening of patients’ specimens (editorial) // Transfus. Med. – 1996. – V. 6. – P. 307–309.

522.Phillips P., Voak D., Knowles S. et al. An explanation and the clinical significance of the failure of microcolumn tests to detect weak AB0 and other antibodies // Transfus. Med. – 1997. – V. 7. – P. 47–53.

523.Phillips P., Voak D., Whitton C.M. et al. BCSH-NIBSC anti-D reference reagent for antiglobulin tests: the in-house assessment of red cell washing centrifuges and of operator variability in the detection of weak, macroscopic agglutination. British Committee for Standards in Haematology. National Institute for Biological Standards and Control // Transfus Med. – 1993. – V. 3. – P. 143–148.

524.PhillipsP.,WhittonC.,LavinF.Theuseoftheantiglobulin«geltest»forantibodydetection

//Transfus. Med. – 1992. – V. 2. – P. 111–113.

525.Pickles M.M. Effects of cholera filtrate on red cells as demonstrated by incomplete Rh antibodies // Nature. – 1946. – V. 158. – Р. 880.

526.Pietrusky F.DasBlutgruppengutachten.–München,Berlin:BeckscheVerlagsbuchhandlung, 1956. –2Aufl.

527.Pinkerton P., Ward J., Chan R., Coovadia A. An evaluation of gel technique for antibody screening compared with a conventional tube method // Transfus. Med. – 1993. – V. 3. –

P.275–279.

528.Pirofsky B., August A., Nelson H., Pittenger R. Rapid mass anti-D (Rho) typing with bromelin // J. Lab. Clin. Med. – 1960. – V. 56. – N 6. – Р. 911.

529.Pirofsky B., Mangum M.E. Use of bromelin to demonstrate erythrocyte antibodies // Proc. Soc. Exptl. Biol. and Med. – 1958. – V. 101. – N 1. – Р. 49.

530.Plapp F.V., Kowalski M.M., Evans J.P. et al. The role of membrane phospholipid in expression of erythrocyte Rho(D) antigen activity // Proc. Soc. Exp. Biol. Med. – 1980. –

V.164. – P. 561–568.

531.Plaut G., Booth P.B., Giles C.M., Mourant A.E. A new example of the antibody, anti-C x // Brit. Med. J. – 1958. – V. I. – Р. 1215–1217.

330