-
1
-
-
0025779323
-
Molecular cloning and primary structure of Kell blood group protein
-
Lee S Zambas ED Marsh WL Molecular cloning and primary structure of Kell blood group protein Proc Natl Acad Sci U S A 88 1991 6353 6357
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 6353-6357
-
-
Lee, S1
Zambas, ED2
Marsh, WL3
-
2
-
-
0028263898
-
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein
-
Ho M Chelly J Carter N Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein Cell 77 1994 869 880
-
(1994)
Cell
, vol.77
, pp. 869-880
-
-
Ho, M1
Chelly, J2
Carter, N3
-
3
-
-
0028933250
-
Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients
-
Khamlichi S Bailly P Blanchard D Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients Eur J Biochem 228 1995 931 934
-
(1995)
Eur J Biochem
, vol.228
, pp. 931-934
-
-
Khamlichi, S1
Bailly, P2
Blanchard, D3
-
4
-
-
0031044711
-
Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides
-
Carbonnet F Hattab C Collec E Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides Br J Haematol 96 1997 857 863
-
(1997)
Br J Haematol
, vol.96
, pp. 857-863
-
-
Carbonnet, F1
Hattab, C2
Collec, E3
-
5
-
-
0032577460
-
Association of XK and Kell blood group proteins
-
Russo D Redman C Lee S Association of XK and Kell blood group proteins J Biol Chem 273 1998 13950 13956
-
(1998)
J Biol Chem
, vol.273
, pp. 13950-13956
-
-
Russo, D1
Redman, C2
Lee, S3
-
6
-
-
0033566651
-
Proteolytic processing of big endothelin-3 by the Kell blood group protein
-
Lee S Lin M Mele A Proteolytic processing of big endothelin-3 by the Kell blood group protein Blood 94 1999 1440 1450
-
(1999)
Blood
, vol.94
, pp. 1440-1450
-
-
Lee, S1
Lin, M2
Mele, A3
-
7
-
-
0025863911
-
Genetic linkage between the Kell blood group system and prolactin-inducible protein loci: provisional assignment of KEL to chromosome 7
-
Zelinski T Coghlan G Myal Y Genetic linkage between the Kell blood group system and prolactin-inducible protein loci: provisional assignment of KEL to chromosome 7 Ann Hum Genet 55 1991 137 140
-
(1991)
Ann Hum Genet
, vol.55
, pp. 137-140
-
-
Zelinski, T1
Coghlan, G2
Myal, Y3
-
8
-
-
0027195281
-
The human Kell blood group gene maps to chromosome 7q33 and its expression is restricted to erythroid cells
-
Lee S Zambas ED Marsh WL The human Kell blood group gene maps to chromosome 7q33 and its expression is restricted to erythroid cells Blood 81 1993 2804 2809
-
(1993)
Blood
, vol.81
, pp. 2804-2809
-
-
Lee, S1
Zambas, ED2
Marsh, WL3
-
9
-
-
0028946052
-
Organization of the gene encoding the human Kell blood group protein
-
Lee S Zambas E Green ED Organization of the gene encoding the human Kell blood group protein Blood 85 1995 1364 1370
-
(1995)
Blood
, vol.85
, pp. 1364-1370
-
-
Lee, S1
Zambas, E2
Green, ED3
-
10
-
-
0023910762
-
Localization of the McLeod locus (XK) within Xp21 by deletion analysis
-
Bertelson CJ Pogo AO Chaudhuri A Localization of the McLeod locus (XK) within Xp21 by deletion analysis Am J Hum Genet 42 1988 703 711
-
(1988)
Am J Hum Genet
, vol.42
, pp. 703-711
-
-
Bertelson, CJ1
Pogo, AO2
Chaudhuri, A3
-
11
-
-
0032578614
-
Kx, a quantitatively minor protein from human erythrocytes, is palmitoylated in vivo
-
Carbonnet F Hattab C Callebaut I Kx, a quantitatively minor protein from human erythrocytes, is palmitoylated in vivo Biochem Biophys Res Commun 250 1998 569 574
-
(1998)
Biochem Biophys Res Commun
, vol.250
, pp. 569-574
-
-
Carbonnet, F1
Hattab, C2
Callebaut, I3
-
12
-
-
0032577894
-
Kell and Kx, two disulfide-linked proteins of the human erythrocyte membrane are phosphorylated in vivo
-
Carbonnet F Hattab C Cartron JP Kell and Kx, two disulfide-linked proteins of the human erythrocyte membrane are phosphorylated in vivo Biochem Biophys Res Commun 247 1998 569 575
-
(1998)
Biochem Biophys Res Commun
, vol.247
, pp. 569-575
-
-
Carbonnet, F1
Hattab, C2
Cartron, JP3
-
13
-
-
0027244617
-
The Kell blood group system and the McLeod phenotype (review)
-
Redman CM Marsh WL The Kell blood group system and the McLeod phenotype (review) Semin Hematol 30 1993 209 218
-
(1993)
Semin Hematol
, vol.30
, pp. 209-218
-
-
Redman, CM1
Marsh, WL2
-
14
-
-
0030899822
-
Mammalian membrane metallopeptidases: NEP, ECE, KELL, and PEX
-
Turner AJ Tanzawa K Mammalian membrane metallopeptidases: NEP, ECE, KELL, and PEX FASEB J 11 1997 355 364
-
(1997)
FASEB J
, vol.11
, pp. 355-364
-
-
Turner, AJ1
Tanzawa, K2
-
15
-
-
0033524706
-
XCE, a new member of the endothelin-converting enzyme and neutral endopeptidase family, is preferentially expressed in the CNS
-
Valdenaire O Richards JG Faull RLM XCE, a new member of the endothelin-converting enzyme and neutral endopeptidase family, is preferentially expressed in the CNS Brain Res Mol Brain Res 64 1999 211 221
-
(1999)
Brain Res Mol Brain Res
, vol.64
, pp. 211-221
-
-
Valdenaire, O1
Richards, JG2
Faull, RLM3
-
16
-
-
0032577463
-
Cloning of human PEX cDNA: Expression, subcellular localization, and endopeptidase activity
-
Lipman ML Panda D Bennett HPJ Cloning of human PEX cDNA: Expression, subcellular localization, and endopeptidase activity J Biol Chem 273 1998 13729 13737
-
(1998)
J Biol Chem
, vol.273
, pp. 13729-13737
-
-
Lipman, ML1
Panda, D2
Bennett, HPJ3
-
17
-
-
0033575285
-
Neonatal lethality in mice deficient in XCE, a novel member of the endothelin-converting enzyme and neutral endopeptidase family
-
Schweizer A Valdenaire O Koster A Neonatal lethality in mice deficient in XCE, a novel member of the endothelin-converting enzyme and neutral endopeptidase family J Biol Chem 274 1999 20450 20456
-
(1999)
J Biol Chem
, vol.274
, pp. 20450-20456
-
-
Schweizer, A1
Valdenaire, O2
Koster, A3
-
18
-
-
0030820550
-
Molecular basis of Kell blood group phenotypes
-
Lee S Molecular basis of Kell blood group phenotypes Vox Sang 73 1997 1 11
-
(1997)
Vox Sang
, vol.73
, pp. 1-11
-
-
Lee, S1
-
19
-
-
0028936247
-
Molecular basis of the Kell (K1) phenotype
-
Lee S Wu X Reid M Molecular basis of the Kell (K1) phenotype Blood 85 1995 912 916
-
(1995)
Blood
, vol.85
, pp. 912-916
-
-
Lee, S1
Wu, X2
Reid, M3
-
20
-
-
0029849311
-
Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2
-
Lee SH Bennett PR Overton T Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2 Am J Obstet Gynecol 175 1996 455 459
-
(1996)
Am J Obstet Gynecol
, vol.175
, pp. 455-459
-
-
Lee, SH1
Bennett, PR2
Overton, T3
-
21
-
-
0030158309
-
Development of a PCR-based diagnostic assay for the determination of KEL genotype in donor blood samples
-
Murphy MT Fraser RH Goddard JP Development of a PCR-based diagnostic assay for the determination of KEL genotype in donor blood samples Transfusion Medicine 6 1996 133 137
-
(1996)
Transfusion Medicine
, vol.6
, pp. 133-137
-
-
Murphy, MT1
Fraser, RH2
Goddard, JP3
-
22
-
-
0029949995
-
Kell typing by allele-specific PCR (ASP)
-
Avent ND Martin PG Kell typing by allele-specific PCR (ASP) Br J Haematol 93 1996 728 730
-
(1996)
Br J Haematol
, vol.93
, pp. 728-730
-
-
Avent, ND1
Martin, PG2
-
23
-
-
0030787899
-
Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies
-
Spence WC Maddalena A Demers DB Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies J Reprod Med 42 1997 353 357
-
(1997)
J Reprod Med
, vol.42
, pp. 353-357
-
-
Spence, WC1
Maddalena, A2
Demers, DB3
-
24
-
-
0030036591
-
Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles
-
Lee S Wu X Son S Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles Transfusion 36 1996 490 494
-
(1996)
Transfusion
, vol.36
, pp. 490-494
-
-
Lee, S1
Wu, X2
Son, S3
-
25
-
-
0033168805
-
Identification of a defect in the intracellular trafficking of a Kell blood group varian
-
Yazdanbakhsh K Lee S Yu Q Identification of a defect in the intracellular trafficking of a Kell blood group varian Blood 94 1999 310 318
-
(1999)
Blood
, vol.94
, pp. 310-318
-
-
Yazdanbakhsh, K1
Lee, S2
Yu, Q3
-
26
-
-
0028889428
-
Molecular basis of the K:6,-7 [Js(a+b−)] phenotype in the Kell blood group system
-
Lee S Wu X Reid M Molecular basis of the K:6,-7 [Js(a+b−)] phenotype in the Kell blood group system Transfusion 35 1995 822 825
-
(1995)
Transfusion
, vol.35
, pp. 822-825
-
-
Lee, S1
Wu, X2
Reid, M3
-
27
-
-
0029928980
-
A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis
-
Ho MF Chalmer RM Davis MB A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis Ann Neurol 39 1996 672 675
-
(1996)
Ann Neurol
, vol.39
, pp. 672-675
-
-
Ho, MF1
Chalmer, RM2
Davis, MB3
-
28
-
-
0033137122
-
A novel frameshift mutation in the McLeod syndrome gene in a Japanese family
-
Hanaoka N Yoshida K Nakamura A A novel frameshift mutation in the McLeod syndrome gene in a Japanese family J Neurol Sci 165 1999 6 9
-
(1999)
J Neurol Sci
, vol.165
, pp. 6-9
-
-
Hanaoka, N1
Yoshida, K2
Nakamura, A3
-
29
-
-
0026781027
-
McLeod syndrome: A distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations
-
Witt TN Danek A Reiter M McLeod syndrome: A distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations J Neurol 239 1992 302 306
-
(1992)
J Neurol
, vol.239
, pp. 302-306
-
-
Witt, TN1
Danek, A2
Reiter, M3
-
30
-
-
0024384505
-
Acanthocytosis and neurological impairment: A review
-
Hardie RJ Acanthocytosis and neurological impairment: A review Q J Med 71 1989 291 306
-
(1989)
Q J Med
, vol.71
, pp. 291-306
-
-
Hardie, RJ1
-
31
-
-
0030032386
-
Molecular pharmacology of endothelin converting enzymes
-
Turner AJ Murphy LJ Molecular pharmacology of endothelin converting enzymes Biochem Pharmacol 51 1996 91 102
-
(1996)
Biochem Pharmacol
, vol.51
, pp. 91-102
-
-
Turner, AJ1
Murphy, LJ2
-
32
-
-
0033041492
-
Structural basis of the function of endothelin receptor
-
Masaki T Ninomiya H Sakamoto A Structural basis of the function of endothelin receptor Mol Cell Biochem 190 1999 153 156
-
(1999)
Mol Cell Biochem
, vol.190
, pp. 153-156
-
-
Masaki, T1
Ninomiya, H2
Sakamoto, A3
-
33
-
-
0028360062
-
Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1
-
Kurihara Y Kurihara H Suzuki H Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1 Nature 368 1994 703 710
-
(1994)
Nature
, vol.368
, pp. 703-710
-
-
Kurihara, Y1
Kurihara, H2
Suzuki, H3
-
34
-
-
0029092767
-
Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1
-
Kurihara Y Kurihara H Oda H Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1 J Clin Invest 96 1995 293 300
-
(1995)
J Clin Invest
, vol.96
, pp. 293-300
-
-
Kurihara, Y1
Kurihara, H2
Oda, H3
-
35
-
-
0031916129
-
Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice
-
Clouthier DE Hosoda K Richardson JA Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice Development 125 1998 813 824
-
(1998)
Development
, vol.125
, pp. 813-824
-
-
Clouthier, DE1
Hosoda, K2
Richardson, JA3
-
36
-
-
0032128263
-
Role of endothelin-1/endothelin-A receptor-mediated signaling pathway in the aortic arch patterning in mice
-
Yanagisawa H Hammer RE Richardson JA Role of endothelin-1/endothelin-A receptor-mediated signaling pathway in the aortic arch patterning in mice J Clin Invest 102 1998 22 33
-
(1998)
J Clin Invest
, vol.102
, pp. 22-33
-
-
Yanagisawa, H1
Hammer, RE2
Richardson, JA3
-
37
-
-
0028609612
-
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
-
Baynash AG Hosoda K Giaid A Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons Cell 79 1994 1277 1285
-
(1994)
Cell
, vol.79
, pp. 1277-1285
-
-
Baynash, AG1
Hosoda, K2
Giaid, A3
-
38
-
-
0028639196
-
Targeted and natural (Piebald-Lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
-
Hosoda K Hammer RE Richardson JA Targeted and natural (Piebald-Lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice Cell 79 1994 1267 1276
-
(1994)
Cell
, vol.79
, pp. 1267-1276
-
-
Hosoda, K1
Hammer, RE2
Richardson, JA3
-
39
-
-
0032006562
-
Ontogeny of endothelins-1 and-3, their receptors, and endothelin converting enzyme-1 in the early human embryo
-
Brand M Le Moullee JM Corvol P Ontogeny of endothelins-1 and-3, their receptors, and endothelin converting enzyme-1 in the early human embryo J Clin Invest 101 1998 549 559
-
(1998)
J Clin Invest
, vol.101
, pp. 549-559
-
-
Brand, M1
Le Moullee, JM2
Corvol, P3
-
40
-
-
0028618372
-
A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
-
Puffenberger EG Hosoda K Washington SS A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease Cell 79 1994 1257 1266
-
(1994)
Cell
, vol.79
, pp. 1257-1266
-
-
Puffenberger, EG1
Hosoda, K2
Washington, SS3
-
41
-
-
0031940499
-
Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene
-
Yanagisawa H Yanagisawa M Kapur RP Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene Development 125 1998 825 836
-
(1998)
Development
, vol.125
, pp. 825-836
-
-
Yanagisawa, H1
Yanagisawa, M2
Kapur, RP3
-
42
-
-
0028987867
-
Possible role of endothelin in endothelial regulation of vascular tone
-
Masaki T Possible role of endothelin in endothelial regulation of vascular tone Annu Rev Pharmacol Toxicol 35 1995 235 255
-
(1995)
Annu Rev Pharmacol Toxicol
, vol.35
, pp. 235-255
-
-
Masaki, T1
-
45
-
-
0028133343
-
Erythropoietic suppression in fetal anemia because of Kell alloimmunization
-
Vaughan JI Warwick R Letsky E Erythropoietic suppression in fetal anemia because of Kell alloimmunization Am J Obstet Gynecol 171 1994 247 252
-
(1994)
Am J Obstet Gynecol
, vol.171
, pp. 247-252
-
-
Vaughan, JI1
Warwick, R2
Letsky, E3
-
47
-
-
0030043703
-
Decreased fetal erythropoiesis and hemolysis in Kell hemolytic anemia
-
Weiner CP Widness JA Decreased fetal erythropoiesis and hemolysis in Kell hemolytic anemia Am J Obstet Gynecol 174 1996 547 551
-
(1996)
Am J Obstet Gynecol
, vol.174
, pp. 547-551
-
-
Weiner, CP1
Widness, JA2
-
48
-
-
0032546227
-
Inhibition of erythroid progenitor cells by anti-Kell antibodies in fetal alloimmune anemia
-
Vaughan JI Manning M Warwick RM Inhibition of erythroid progenitor cells by anti-Kell antibodies in fetal alloimmune anemia N Engl J Med 338 1998 798 803
-
(1998)
N Engl J Med
, vol.338
, pp. 798-803
-
-
Vaughan, JI1
Manning, M2
Warwick, RM3
-
49
-
-
0033564954
-
The expression of human blood group antigens during erythropoiesis in a cell culture system
-
Southcott MG Tanner MA Anstee DJ The expression of human blood group antigens during erythropoiesis in a cell culture system Blood 93 1999 4425 4435
-
(1999)
Blood
, vol.93
, pp. 4425-4435
-
-
Southcott, MG1
Tanner, MA2
Anstee, DJ3
|