-
1
-
-
33644870599
-
Identification of two new members, XPLAC and XTES, of the XK family
-
Calenda G, Peng J, Redman CM, Sha Q, Wu X, Lee S (2006) Identification of two new members, XPLAC and XTES, of the XK family. Gene 370:6-16
-
(2006)
Gene
, vol.370
, pp. 6-16
-
-
Calenda, G.1
Peng, J.2
Redman, C.M.3
Sha, Q.4
Wu, X.5
Lee, S.6
-
2
-
-
0035874484
-
Transcriptional regulation of the KEL gene and Kell protein expression in erythroid and non-erythroid cells
-
Camara-Clayette V, Rahuel C, Lopez C, Hattab C, Verkarre V, Bertrand O, Cartron JP (2001) Transcriptional regulation of the KEL gene and Kell protein expression in erythroid and non-erythroid cells. Biochem J 356:171-180
-
(2001)
Biochem J
, vol.356
, pp. 171-180
-
-
Camara-Clayette, V.1
Rahuel, C.2
Lopez, C.3
Hattab, C.4
Verkarre, V.5
Bertrand, O.6
Cartron, J.P.7
-
3
-
-
0035202829
-
McLeod neuroacanthocytosis: Genotype and phenotype
-
Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, et al. (2001a) McLeod neuroacanthocytosis: genotype and phenotype. Ann Neurol 50:755-764
-
(2001)
Ann Neurol
, vol.50
, pp. 755-764
-
-
Danek, A.1
Rubio, J.P.2
Rampoldi, L.3
Ho, M.4
Dobson-Stone, C.5
Tison, F.6
Symmans, W.A.7
-
4
-
-
0035470417
-
The chorea of McLeod syndrome
-
Danek A, Tison F, Rubio J, Oechsner M, Kalckreuth W, Monaco AP (2001b) The chorea of McLeod syndrome. Mov Disord 16: 882-889
-
(2001)
Mov Disord
, vol.16
, pp. 882-889
-
-
Danek, A.1
Tison, F.2
Rubio, J.3
Oechsner, M.4
Kalckreuth, W.5
Monaco, A.P.6
-
5
-
-
0027958727
-
Cerebral involvement in McLeod syndrome
-
Danek A, Uttner I, Vogl T, Tatsch K, Witt TN (1994) Cerebral involvement in McLeod syndrome. Neurology 44:117-120
-
(1994)
Neurology
, vol.44
, pp. 117-120
-
-
Danek, A.1
Uttner, I.2
Vogl, T.3
Tatsch, K.4
Witt, T.N.5
-
6
-
-
0029826394
-
A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cells
-
Daniels GL, Weinauer F, Stone C, Ho M, Green CA, Jahn-Jochem H, Offner R, et al. (1996) A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cells. Blood 88:4045-4050
-
(1996)
Blood
, vol.88
, pp. 4045-4050
-
-
Daniels, G.L.1
Weinauer, F.2
Stone, C.3
Ho, M.4
Green, C.A.5
Jahn-Jochem, H.6
Offner, R.7
-
7
-
-
0026051936
-
Genes required for the engulfment of cell corpses during programmed cell death in Caenorhabditis elegans
-
Ellis RE, Jacobson DM, Horvitz HR (1991) Genes required for the engulfment of cell corpses during programmed cell death in Caenorhabditis elegans. Genetics 129:79-94
-
(1991)
Genetics
, vol.129
, pp. 79-94
-
-
Ellis, R.E.1
Jacobson, D.M.2
Horvitz, H.R.3
-
8
-
-
0035097069
-
Editorial: Gonadal-specific transcription factors-gata (go) 4 it!
-
Hales DB (2001) Editorial: gonadal-specific transcription factors-gata (go) 4 it! Endocrinology 142:974-976
-
(2001)
Endocrinology
, vol.142
, pp. 974-976
-
-
Hales, D.B.1
-
9
-
-
0028263898
-
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein
-
Ho M, Chelly J, Carter N, Danek A, Crocker P, Monaco AP (1994) Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. Cell 77:869-880
-
(1994)
Cell
, vol.77
, pp. 869-880
-
-
Ho, M.1
Chelly, J.2
Carter, N.3
Danek, A.4
Crocker, P.5
Monaco, A.P.6
-
10
-
-
0038307154
-
McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement
-
Jung HH, Hergersberg M, Vogt M, Pahnke J, Treyer V, Rothlisberger B, Kollias SS, et al. (2003) McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement. Transfusion 43:928-938
-
(2003)
Transfusion
, vol.43
, pp. 928-938
-
-
Jung, H.H.1
Hergersberg, M.2
Vogt, M.3
Pahnke, J.4
Treyer, V.5
Rothlisberger, B.6
Kollias, S.S.7
-
12
-
-
0028933250
-
Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients
-
Khamlichi S, Bailly P, Blanchard D, Goossens D, Cartron JP, Bertrand O (1995) Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients. Eur J Biochem 228: 931-934
-
(1995)
Eur J Biochem
, vol.228
, pp. 931-934
-
-
Khamlichi, S.1
Bailly, P.2
Blanchard, D.3
Goossens, D.4
Cartron, J.P.5
Bertrand, O.6
-
13
-
-
0030820550
-
Molecular basis of Kell blood group phenotypes
-
Lee S (1997) Molecular basis of Kell blood group phenotypes. Vox Sang 73:1-11
-
(1997)
Vox Sang
, vol.73
, pp. 1-11
-
-
Lee, S.1
-
14
-
-
33746370373
-
Molecular basis of two novel high-prevalence antigens in the Kell blood group system, KALT and KTIM
-
Lee S, Debnath AK, Wu X, Scofield T, George T, Kakaiya R, Yogore MG III, et al. (2006) Molecular basis of two novel high-prevalence antigens in the Kell blood group system, KALT and KTIM. Transfusion 46:1323-1327
-
(2006)
Transfusion
, vol.46
, pp. 1323-1327
-
-
Lee, S.1
Debnath, A.K.2
Wu, X.3
Scofield, T.4
George, T.5
Kakaiya, R.6
Yogore III, M.G.7
-
15
-
-
0033566651
-
Proteolytic processing of big endothelin-3 by the Kell blood group protein
-
Lee S, Lin M, Mele A, Cao Y, Farmar J, Russo D, Redman C (1999) Proteolytic processing of big endothelin-3 by the Kell blood group protein. Blood 94:1440-1450
-
(1999)
Blood
, vol.94
, pp. 1440-1450
-
-
Lee, S.1
Lin, M.2
Mele, A.3
Cao, Y.4
Farmar, J.5
Russo, D.6
Redman, C.7
-
16
-
-
0034031642
-
Functional and structural aspects of the Kell blood group system
-
Lee S, Russo D, Redman C (2000a) Functional and structural aspects of the Kell blood group system. Transfus Med Rev 14:93-103
-
(2000)
Transfus Med Rev
, vol.14
, pp. 93-103
-
-
Lee, S.1
Russo, D.2
Redman, C.3
-
17
-
-
0034081001
-
The Kell blood group system: Kell and XK membrane proteins
-
Lee S, Russo D, Redman CM (2000b) The Kell blood group system: Kell and XK membrane proteins. Semin Hematol 37:113-121
-
(2000)
Semin Hematol
, vol.37
, pp. 113-121
-
-
Lee, S.1
Russo, D.2
Redman, C.M.3
-
18
-
-
0035920205
-
Molecular defects underlying the Kell null phenotype
-
Lee S, Russo DC, Reiner AP, Lee JH, Sy MY, Telen MJ, Judd WJ, et al. (2001) Molecular defects underlying the Kell null phenotype. J Biol Chem 276:27281-27289
-
(2001)
J Biol Chem
, vol.276
, pp. 27281-27289
-
-
Lee, S.1
Russo, D.C.2
Reiner, A.P.3
Lee, J.H.4
Sy, M.Y.5
Telen, M.J.6
Judd, W.J.7
-
19
-
-
0028946052
-
Organization of the gene encoding the human Kell blood group protein
-
Lee S, Zambas E, Green ED, Redman C (1995) Organization of the gene encoding the human Kell blood group protein. Blood 85: 1364-1370
-
(1995)
Blood
, vol.85
, pp. 1364-1370
-
-
Lee, S.1
Zambas, E.2
Green, E.D.3
Redman, C.4
-
21
-
-
0025608774
-
Developmental regulation of myosin gene expression in mouse cardiac muscle
-
Lyons GE, Schiaffino S, Sassoon D, Barton P, Buckingham M (1990) Developmental regulation of myosin gene expression in mouse cardiac muscle. J Cell Biol 111:2427-2436
-
(1990)
J Cell Biol
, vol.111
, pp. 2427-2436
-
-
Lyons, G.E.1
Schiaffino, S.2
Sassoon, D.3
Barton, P.4
Buckingham, M.5
-
22
-
-
0028227820
-
Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: Report of a family
-
Malandrini A, Fabrizi GM, Truschi F, Di Pietro G, Moschini F, Bartalucci P, Berti G, et al. (1994) Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family. J Neurol Sci 124:89-94
-
(1994)
J Neurol Sci
, vol.124
, pp. 89-94
-
-
Malandrini, A.1
Fabrizi, G.M.2
Truschi, F.3
Di Pietro, G.4
Moschini, F.5
Bartalucci, P.6
Berti, G.7
-
23
-
-
0028987867
-
Possible role of endothelin in endothelial regulation of vascular tone
-
Masaki T (1995) Possible role of endothelin in endothelial regulation of vascular tone. Annu Rev Pharmacol Toxicol 35:235-255
-
(1995)
Annu Rev Pharmacol Toxicol
, vol.35
, pp. 235-255
-
-
Masaki, T.1
-
24
-
-
0034806070
-
EDNRB/EDN3 and Hirschsprung disease type II
-
McCallion AS, Chakravarti A (2001) EDNRB/EDN3 and Hirschsprung disease type II. Pigment Cell Res 14:161-169
-
(2001)
Pigment Cell Res
, vol.14
, pp. 161-169
-
-
McCallion, A.S.1
Chakravarti, A.2
-
25
-
-
33745754627
-
Induction of melanocytes from embryonic stem cells and their therapeutic potential
-
Motohashi T, Aoki H, Yoshimura N, Kunisada T (2006) Induction of melanocytes from embryonic stem cells and their therapeutic potential. Pigment Cell Res 19:284-289
-
(2006)
Pigment Cell Res
, vol.19
, pp. 284-289
-
-
Motohashi, T.1
Aoki, H.2
Yoshimura, N.3
Kunisada, T.4
-
26
-
-
33646028213
-
Endothelin-3 regulates neural crest cell proliferation and differentiation in the hindgut enteric nervous system
-
Nagy N, Goldstein AM (2006) Endothelin-3 regulates neural crest cell proliferation and differentiation in the hindgut enteric nervous system. Dev Biol 293:203-217
-
(2006)
Dev Biol
, vol.293
, pp. 203-217
-
-
Nagy, N.1
Goldstein, A.M.2
-
27
-
-
0027253994
-
Isolated sequences from the linked Myf-5 and MRF4 genes drive distinct patterns of muscle-specific expression in transgenic mice
-
Patapoutian A, Miner JH, Lyons GE, Wold B (1993) Isolated sequences from the linked Myf-5 and MRF4 genes drive distinct patterns of muscle-specific expression in transgenic mice. Development 118:61-69
-
(1993)
Development
, vol.118
, pp. 61-69
-
-
Patapoutian, A.1
Miner, J.H.2
Lyons, G.E.3
Wold, B.4
-
28
-
-
0033387316
-
Intracellular assembly of Kell and XK blood group proteins
-
Russo D, Lee S, Redman C (1999) Intracellular assembly of Kell and XK blood group proteins. Biochim Biophys Acta 1461:10-18
-
(1999)
Biochim Biophys Acta
, vol.1461
, pp. 10-18
-
-
Russo, D.1
Lee, S.2
Redman, C.3
-
29
-
-
0032577460
-
Association of XK and Kell blood group proteins
-
Russo D, Redman C, Lee S (1998) Association of XK and Kell blood group proteins. J Biol Chem 273:13950-13956
-
(1998)
J Biol Chem
, vol.273
, pp. 13950-13956
-
-
Russo, D.1
Redman, C.2
Lee, S.3
-
30
-
-
0034235469
-
Expression of Kell blood group protein in nonerythroid tissues
-
Russo D, Wu X, Redman CM, Lee S (2000) Expression of Kell blood group protein in nonerythroid tissues. Blood 96:340-346
-
(2000)
Blood
, vol.96
, pp. 340-346
-
-
Russo, D.1
Wu, X.2
Redman, C.M.3
Lee, S.4
-
32
-
-
0033680282
-
The ced-8 gene controls the timing of programmed cell deaths in C. elegans
-
Stanfield GM, Horvitz HR (2000) The ced-8 gene controls the timing of programmed cell deaths in C. elegans. Mol Cell 5:423-433
-
(2000)
Mol Cell
, vol.5
, pp. 423-433
-
-
Stanfield, G.M.1
Horvitz, H.R.2
-
33
-
-
33846418770
-
McLeod phenotype without the McLeod syndrome
-
Walker RH, Danek A, Uttner I, Offner R, Reid M, Lee S (2007) McLeod phenotype without the McLeod syndrome. Transfusion 47:299-305
-
(2007)
Transfusion
, vol.47
, pp. 299-305
-
-
Walker, R.H.1
Danek, A.2
Uttner, I.3
Offner, R.4
Reid, M.5
Lee, S.6
-
34
-
-
0010375035
-
Mesencephalic dopamine neurons regulate the expression of neuropeptide mRNAs in the rat forebrain
-
Young WS III, Bonner TI, Brann MR (1986) Mesencephalic dopamine neurons regulate the expression of neuropeptide mRNAs in the rat forebrain. Proc Natl Acad Sci USA 83:9827-9831
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 9827-9831
-
-
Young III, W.S.1
Bonner, T.I.2
Brann, M.R.3
|