-
1
-
-
35348822545
-
Velocardiofacial syndrome, DiGeorge syndrome: The chromosome 22q11.2 deletion syndromes
-
DOI 10.1016/S0140-6736(07)61601-8, PII S0140673607616018
-
LJ Kobrynski KE Sullivan 2007 Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes Lancet 370 1443 1452 17950858 10.1016/S0140-6736(07)61601-8 1:CAS:528:DC%2BD2sXhtF2hu7rM (Pubitemid 47576169)
-
(2007)
Lancet
, vol.370
, Issue.9596
, pp. 1443-1452
-
-
Kobrynski, L.J.1
Sullivan, K.E.2
-
2
-
-
0036889598
-
Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes)
-
DOI 10.1097/00008480-200212000-00005
-
E Perez KE Sullivan 2002 Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes) Curr Opin Pediatr 14 678 683 12436034 10.1097/00008480-200212000-00005 (Pubitemid 35333127)
-
(2002)
Current Opinion in Pediatrics
, vol.14
, Issue.6
, pp. 678-683
-
-
Perez, E.1
Sullivan, K.E.2
-
4
-
-
0141458167
-
Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome
-
DOI 10.1016/S1471-4914(03)00141-2
-
H Yamagashi D Srivastava 2003 Unravelling the genetic and developmental mysteries of 22q11 deletion syndrome Trends Mol Med 9 383 389 10.1016/S1471-4914(03)00141-2 (Pubitemid 37169052)
-
(2003)
Trends in Molecular Medicine
, vol.9
, Issue.9
, pp. 383-389
-
-
Yamagishi, H.1
Srivastava, D.2
-
5
-
-
0035098557
-
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
-
DOI 10.1038/85845
-
LA Jerome VE Papaioannou 2001 DiGeorge syndrome phenotype in mice mutant for the T box gene, Tbx1 Nat Genet 27 286 291 11242110 10.1038/85845 1:CAS:528:DC%2BD3MXhslOjur8%3D (Pubitemid 32201849)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 286-291
-
-
Jerome, L.A.1
Papaioannou, V.E.2
-
6
-
-
0000025287
-
A new concept of the cellular basis of immunity
-
10.1016/S0022-3476(65)81796-6
-
MD Cooper RDA Peterson RA Good 1965 A new concept of the cellular basis of immunity J Pediatr 67 907 908 10.1016/S0022-3476(65)81796-6
-
(1965)
J Pediatr
, vol.67
, pp. 907-908
-
-
Cooper, M.D.1
Peterson, R.D.A.2
Good, R.A.3
-
8
-
-
0020026258
-
The association of the DiGeorge anomalad with partial monosomy of chromosome 22
-
DOI 10.1016/S0022-3476(82)80116-9
-
RI Kelley EH Zackai BS Emanuel M Kistenmacher F Greenberg HH Punnett 1982 The association of the DiGeorge anomalad with partial monosomy of chromosome 22 J Pediatr 101 197 200 7097410 10.1016/S0022-3476(82)80116-9 1:STN:280:DyaL383ktFCjtQ%3D%3D (Pubitemid 12098766)
-
(1982)
Journal of Pediatrics
, vol.101
, Issue.2
, pp. 197-200
-
-
Kelly, R.I.1
Zackai, E.H.2
Emanuel, B.S.3
-
9
-
-
0026662962
-
Deletions and microdeletions of 22q11.2 in velo-cardio-fa-cial syndrome
-
1360769 10.1002/ajmg.1320440237 1:STN:280:DyaK3s%2FovFelsQ%3D%3D
-
DA Driscoll NB Spinner ML Budarf DM McDonald-McGinn EH Zackai RB Goldberg RJ Shprintzen HM Saal J Zonana MC Jones 1992 Deletions and microdeletions of 22q11.2 in velo-cardio-fa-cial syndrome Am J Med Genet 44 261 268 1360769 10.1002/ajmg.1320440237 1:STN:280:DyaK3s%2FovFelsQ%3D%3D
-
(1992)
Am J Med Genet
, vol.44
, pp. 261-268
-
-
Driscoll, D.A.1
Spinner, N.B.2
Budarf, M.L.3
McDonald-Mcginn, D.M.4
Zackai, E.H.5
Goldberg, R.B.6
Shprintzen, R.J.7
Saal, H.M.8
Zonana, J.9
Jones, M.C.10
-
10
-
-
0028019184
-
Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2
-
DOI 10.1002/ajmg.1320530314
-
R Matsuoka A Takao M Kimura S Imamura C Kondo K Joh-o K Ikeda M Nishibatake M Ando K Momma 1994 Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2 Am J Med Genet 53 285 289 7856665 10.1002/ajmg.1320530314 1:STN:280:DyaK2M7mtVSnsg%3D%3D (Pubitemid 24362425)
-
(1994)
American Journal of Medical Genetics
, vol.53
, Issue.3
, pp. 285-289
-
-
Matsuoka, R.1
Takao, A.2
Kimura, M.3
Imamura, S.-I.4
Kondo, C.5
Joh-o, K.6
Ikeda, K.7
Nishibatake, M.8
Ando, M.9
Momma, K.10
-
11
-
-
0029148704
-
Autosomal dominant "opitz" GBBB syndrome due to a 22q11.2 deletion
-
8849001 10.1002/ajmg.1320590122 1:STN:280:DyaK287ht1Cgsg%3D%3D
-
DM McDonald-McGinn DA Driscoll L Bason K Christensen D Lynch K Sullivan D Canning W Zavod N Quinn J Rome 1995 Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion Am J Med Genet 59 103 113 8849001 10.1002/ajmg.1320590122 1:STN:280:DyaK287ht1Cgsg%3D%3D
-
(1995)
Am J Med Genet
, vol.59
, pp. 103-113
-
-
McDonald-Mcginn, D.M.1
Driscoll, D.A.2
Bason, L.3
Christensen, K.4
Lynch, D.5
Sullivan, K.6
Canning, D.7
Zavod, W.8
Quinn, N.9
Rome, J.10
-
12
-
-
0031799613
-
Deletion in chromosome region 22q11 in a child with CHARGE association
-
K Devriendt A Swillen JP Fryns 1998 Deletion in chromosome region 22q11 in a child with CHARGE association Clin Genet 53 408 410 9660062 10.1111/j.1399-0004.1998.tb02755.x 1:STN:280:DyaK1czitFCquw%3D%3D (Pubitemid 28252107)
-
(1998)
Clinical Genetics
, vol.53
, Issue.5
, pp. 408-410
-
-
Devriendt, K.1
Swillen, A.2
Fryns, J.-P.3
-
13
-
-
10744223651
-
Role of TBX1 in human del22q11.2 syndrome
-
DOI 10.1016/S0140-6736(03)14632-6
-
H Yagi Y Furutani H Hamada T Sasaki S Asakawa S Minoshima F Ichida K Joo M Kimura S Imamura N Kamatani K Momma A Takao M Nakazawa N Shimizu R Matsuoka 2003 Role of TBX1 in human del22q11.2 syndrome Lancet 362 1366 1373 14585638 10.1016/S0140-6736(03)14632-6 1:CAS:528:DC%2BD3sXosVKkurs%3D (Pubitemid 37338337)
-
(2003)
Lancet
, vol.362
, Issue.9393
, pp. 1366-1373
-
-
Yagi, H.1
Furutani, Y.2
Hamada, H.3
Sasaki, T.4
Asakawa, S.5
Minoshima, S.6
Ichida, F.7
Joo, K.8
Kimura, M.9
Imamura, S.-I.10
Kamatani, N.11
Momma, K.12
Takao, A.13
Nakazawa, M.14
Shimizu, N.15
Matsuoka, R.16
-
14
-
-
0022504844
-
Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome
-
F Greenberg C Valdes HM Rosenblatt JL Kirkland DH Ledbetter 1986 Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome J Pediatr 109 489 492 3509963 10.1016/S0022-3476(86)80124-X 1:STN:280:DyaL28zgsleiuw%3D%3D (Pubitemid 16014278)
-
(1986)
Journal of Pediatrics
, vol.109
, Issue.3
, pp. 489-492
-
-
Greenberg, F.1
Valdes, C.2
Rosenblatt, H.3
-
15
-
-
0024720431
-
T cell immunodeficiency in a patient with 10p deletion syndrome
-
2754563 1:STN:280:DyaL1MzivVOjuw%3D%3D
-
G Monaco F Ciccimarra C Pignata S Garofalo 1989 T cell immunodeficiency in a patient with 10p deletion syndrome J Pediatr 115 330 2754563 1:STN:280:DyaL1MzivVOjuw%3D%3D
-
(1989)
J Pediatr
, vol.115
, pp. 330
-
-
Monaco, G.1
Ciccimarra, F.2
Pignata, C.3
Garofalo, S.4
-
16
-
-
0025852989
-
DiGeorge anomaly associated with 10p deletion
-
2063928 10.1002/ajmg.1320390220 1:STN:280:DyaK3M3ptVWhtQ%3D%3D
-
G Monaco C Pignata E Rossi O Mascellaro S Cocozza F Ciccimarra 1991 DiGeorge anomaly associated with 10p deletion Am J Med Genet 39 215 216 2063928 10.1002/ajmg.1320390220 1:STN:280:DyaK3M3ptVWhtQ%3D%3D
-
(1991)
Am J Med Genet
, vol.39
, pp. 215-216
-
-
Monaco, G.1
Pignata, C.2
Rossi, E.3
Mascellaro, O.4
Cocozza, S.5
Ciccimarra, F.6
-
17
-
-
0032007010
-
Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes (DiGeorge syndrome/velocardiofacial syndrome)
-
DOI 10.1006/clin.1997.4463
-
KE Sullivan AF Jawad P Randall DA Driscoll BS Emanuel DM McDonald-McGinn EH Zackai 1998 Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes Clin Immunol Immunopathol 86 141 146 9473376 10.1006/clin.1997.4463 1:STN:280:DyaK1c7ktF2qtA%3D%3D (Pubitemid 28081550)
-
(1998)
Clinical Immunology and Immunopathology
, vol.86
, Issue.2
, pp. 141-146
-
-
Sullivan, K.E.1
Jawad, A.F.2
Randall, P.3
Driscoll, D.A.4
Emanuel, B.S.5
McDonald-Mcginn, D.M.6
Zackai, E.H.7
-
18
-
-
33645121876
-
Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins
-
16118347 10.1136/jmg.2005.032946 1:CAS:528:DC%2BD28XjsFams78%3D
-
D Johnson N Morrison L Grant T Turner J Fantes JM Connor V Murday 2006 Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins J Med Genet 43 280 284 16118347 10.1136/jmg.2005.032946 1:CAS:528:DC%2BD28XjsFams78%3D
-
(2006)
J Med Genet
, vol.43
, pp. 280-284
-
-
Johnson, D.1
Morrison, N.2
Grant, L.3
Turner, T.4
Fantes, J.5
Connor, J.M.6
Murday, V.7
-
19
-
-
44949125693
-
Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome
-
DOI 10.1111/j.1365-2249.2008.03681.x
-
AR Gennery MA Slatter J Rice LH Hoefsloot D Barge A McLean-Tooke T Montgomery JA Goodship AD Burt TJ Flood M Abinun AJ Cant D Johnson 2008 Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell+ severe combined immune deficiency and may cause Omenn-like syndrome Clin Exp Immunol 153 75 80 18505430 10.1111/j.1365-2249.2008.03681.x 1:STN:280:DC%2BD1cvgs1ajtg%3D%3D (Pubitemid 351809347)
-
(2008)
Clinical and Experimental Immunology
, vol.153
, Issue.1
, pp. 75-80
-
-
Gennery, A.R.1
Slatter, M.A.2
Rice, J.3
Hoefsloot, L.H.4
Barge, D.5
McLean-Tooke, A.6
Montgomery, T.7
Goodship, J.A.8
Burt, A.D.9
Flood, T.J.10
Abinun, M.11
Cant, A.J.12
Johnson, D.13
-
20
-
-
16944364251
-
Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients
-
C Carlson H Sirotkin R Pandita R Goldberg J McKie R Wadey SR Patanjali SM Weissman K Anyane-Yeboa D Warburton P Scrambler R Shprintzen R Kucherlapati BE Morrow 1997 Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients Am J Hum Genet 61 620 629 9326327 10.1086/515508 1:CAS:528:DyaK2sXmsV2ks7w%3D (Pubitemid 27418403)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.3
, pp. 620-629
-
-
Carlson, C.1
Sirotkin, H.2
Pandita, R.3
Goldberg, R.4
McKie, J.5
Wadey, R.6
Patanjali, S.R.7
Weissman, S.M.8
Anyane-Yeboa, K.9
Warburton, D.10
Scambler, P.11
Shprintzen, R.12
Kucherlapati, R.13
Morrow, B.E.14
-
21
-
-
0033358588
-
Low-copy repeats mediate the common 3-Mb deletion in patients with velo- cardio-facial syndrome
-
DOI 10.1086/302343
-
L Edelmann RK Pandita BE Morrow 1999 Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome Am J Hum Genet 64 1076 1086 10090893 10.1086/302343 1:STN:280:DyaK1M7pt1emtg%3D%3D (Pubitemid 30463039)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.4
, pp. 1076-1086
-
-
Edelmann, L.1
Pandita, R.K.2
Morrow, B.E.3
-
22
-
-
34548094068
-
When half is not enough: Gene expression and dosage in the 22q11 Deletion syndrome
-
DOI 10.3727/000000006781510697
-
DW Meechan TM Maynard D Gopalakrishna Y Wu AS LaMantia 2007 When half is not enough: gene expression and dosage in the 22q11 deletion syndrome Gene Expr 13 299 310 17708416 10.3727/000000006781510697 1:STN:280:DC%2BD2svovFyjsQ%3D%3D (Pubitemid 47289403)
-
(2007)
Gene Expression
, vol.13
, Issue.6
, pp. 299-310
-
-
Meechan, D.W.1
Maynard, T.M.2
Gopalakrishna, D.3
Wu, Y.4
LaMantia, A.-S.5
-
24
-
-
0035096508
-
Deconstructing DiGeorge syndrome
-
DOI 10.1038/85784
-
M Schinke S Izumo 2001 Deconstructing DiGeorge syndrome Nat Genet 27 238 240 11242098 10.1038/85784 1:CAS:528:DC%2BD3MXhslCrtLs%3D (Pubitemid 32201840)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 238-240
-
-
Schinke, M.1
Izumo, S.2
-
25
-
-
0035098557
-
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
-
DOI 10.1038/85845
-
LA Jerome VE Papaioannou 2001 DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 Nat Genet 27 286 291 11242110 10.1038/85845 1:CAS:528:DC%2BD3MXhslOjur8%3D (Pubitemid 32201849)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 286-291
-
-
Jerome, L.A.1
Papaioannou, V.E.2
-
26
-
-
0035098436
-
Mice lacking the homologue of the human 22q11.2 gene CRLK phenocopy neurocristopathies of DiGeorge syndrome
-
DOI 10.1038/85855
-
DL Guris J Fantes D Tara BJ Druker A Imamoto 2001 Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome Nat Genet 27 293 298 11242111 10.1038/85855 1:CAS:528:DC%2BD3MXhslOjurs%3D (Pubitemid 32201850)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 293-298
-
-
Guris, D.L.1
Fantes, J.2
Tara, D.3
Druker, B.J.4
Imamoto, A.5
-
27
-
-
29744455342
-
Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome
-
DOI 10.1016/j.devcel.2005.12.002, PII S1534580705004788
-
DL Guris G Duester VE Papaioannou A Imamoto 2006 Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome Dev Cell 10 81 92 16399080 10.1016/j.devcel.2005.12.002 1:CAS:528:DC%2BD28Xht1Sqt7Y%3D (Pubitemid 43025679)
-
(2006)
Developmental Cell
, vol.10
, Issue.1
, pp. 81-92
-
-
Guris, D.L.1
Duester, G.2
Papaioannou, V.E.3
Imamoto, A.4
-
28
-
-
77951203831
-
Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome
-
20122914 10.1016/j.ydbio.2010.01.020
-
KL van Bueren I Papangeli F Rochais K Pearce C Roberts A Calmont D Szumska RG Kelly S Bhattacharya PJ Scambler 2010 Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome Dev Biol 340 369 380 20122914 10.1016/j.ydbio.2010.01. 020
-
(2010)
Dev Biol
, vol.340
, pp. 369-380
-
-
Van Bueren, K.L.1
Papangeli, I.2
Rochais, F.3
Pearce, K.4
Roberts, C.5
Calmont, A.6
Szumska, D.7
Kelly, R.G.8
Bhattacharya, S.9
Scambler, P.J.10
-
30
-
-
34548474527
-
Chromatin remodeling proteins interact with pericentrin to regulate centrosome integrity
-
DOI 10.1091/mbc.E06-07-0604
-
JE Sillibourne B Delaval S Redick M Sinah SJ Doxsey 2007 Chromatin remodeling proteins interact with pericentrin to regulate centrosome integrity Mol Biol Cell 18 3667 3680 17626165 10.1091/mbc.E06-07-0604 1:CAS:528: DC%2BD2sXhtVWntL7M (Pubitemid 47378703)
-
(2007)
Molecular Biology of the Cell
, vol.18
, Issue.9
, pp. 3667-3680
-
-
Sillibourne, J.E.1
Delaval, B.2
Redick, S.3
Sinha, M.4
Doxsey, S.J.5
-
31
-
-
33846030508
-
Embryonic expression profile of chicken Chd7, the ortholog of the causative gene for CHARGE syndrome
-
DOI 10.1002/bdra.20330
-
M Aramaki T Kimura T Udaka R Kosaki T Mitsuhashi Y Okada T Takahashi K Kosaki 2007 Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome Birth Defects Res A Clin Mol Teratol 79 50 57 17149726 10.1002/bdra.20330 1:CAS:528:DC%2BD2sXmsleiuw%3D%3D (Pubitemid 46053411)
-
(2007)
Birth Defects Research Part A - Clinical and Molecular Teratology
, vol.79
, Issue.1
, pp. 50-57
-
-
Aramaki, M.1
Kimura, T.2
Udaka, T.3
Kosaki, R.4
Mitsuhashi, T.5
Okada, Y.6
Takahashi, T.7
Kosaki, K.8
-
32
-
-
33645128921
-
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
-
16169932 10.1136/jmg.2005.036160 1:CAS:528:DC%2BD28XjsFanurY%3D
-
D Sanlaville HC Etchevers M Gonzales J Martinovic M Clément-Ziza AL Delezoide MC Aubry A Pelet S Chemouny C Cruaud S Audollent C Esculpavit G Goudefroye C Ozilou C Fredouille N Joye N Morichon-Delvallez Y Dumez J Weissenbach A Munnich J Amiel F Encha-Razavi S Lyonnet M Vekemans T Attié-Bitach 2006 Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development J Med Genet 43 211 217 16169932 10.1136/jmg.2005.036160 1:CAS:528: DC%2BD28XjsFanurY%3D
-
(2006)
J Med Genet
, vol.43
, pp. 211-217
-
-
Sanlaville, D.1
Etchevers, H.C.2
Gonzales, M.3
Martinovic, J.4
Clément-Ziza, M.5
Delezoide, A.L.6
Aubry, M.C.7
Pelet, A.8
Chemouny, S.9
Cruaud, C.10
Audollent, S.11
Esculpavit, C.12
Goudefroye, G.13
Ozilou, C.14
Fredouille, C.15
Joye, N.16
Morichon-Delvallez, N.17
Dumez, Y.18
Weissenbach, J.19
Munnich, A.20
Amiel, J.21
Encha-Razavi, F.22
Lyonnet, S.23
Vekemans, M.24
Attié-Bitach, T.25
more..
-
33
-
-
16944363108
-
Features of DiGeorge syndrome and CHARGE association in five patients
-
P de Lonlay-Debeney V Cormier-Daire J Amiel V Abadie S Odent A Paupe S Couderc AL Tellier D Bonnet M Prieur M Vekemans A Munnich S Lyonnet 1997 Features of DiGeorge syndrome and CHARGE association in five patients J Med Genet 34 986 989 9429139 10.1136/jmg.34.12.986 (Pubitemid 27522102)
-
(1997)
Journal of Medical Genetics
, vol.34
, Issue.12
, pp. 986-989
-
-
De Lonlay-Debeney, P.1
Cormier-Daire, V.2
Amiel, J.3
Abadie, V.4
Odent, S.5
Paupe, A.6
Couderc, S.7
Tellier, A.-L.8
Bonnet, D.9
Prieur, M.10
Vekemans, M.11
Munnich, A.12
Lyonnet, S.13
-
34
-
-
34248381768
-
Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: Outcome of 44 consecutive transplants
-
DOI 10.1182/blood-2006-10-048652
-
ML Markert BH Devlin MJ Alexieff J Li EA McCarthy SE Gupton IK Chinn LP Hale TB Kepler M He M Sarzotti MA Skinner HE Rice JC Hoehner 2007 Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants Blood 109 4539 4547 17284531 10.1182/blood-2006-10-048652 1:CAS:528:DC%2BD2sXls1amtr8%3D (Pubitemid 46743425)
-
(2007)
Blood
, vol.109
, Issue.10
, pp. 4539-4547
-
-
Markert, M.L.1
Devlin, B.H.2
Alexieff, M.J.3
Li, J.4
McCarthy, E.A.5
Gupton, S.E.6
Chinn, I.K.7
Hale, L.P.8
Kepler, T.B.9
He, M.10
Sarzotti, M.11
Skinner, M.A.12
Rice, H.E.13
Hoehner, J.C.14
-
35
-
-
33645091616
-
Cellular and molecular events during early thymus development
-
16448532 10.1111/j.0105-2896.2006.00357.x
-
G Holländer J Gill S Zuklys N Iwanami C Liu Y Takahama 2006 Cellular and molecular events during early thymus development Immunol Rev 209 28 46 16448532 10.1111/j.0105-2896.2006.00357.x
-
(2006)
Immunol Rev
, vol.209
, pp. 28-46
-
-
Holländer, G.1
Gill, J.2
Zuklys, S.3
Iwanami, N.4
Liu, C.5
Takahama, Y.6
-
36
-
-
0016746976
-
Mesenchymal derivatives of the neural crest: Analysis of chimeric quail and chick embryos
-
1185098 1:STN:280:DyaE28%2FkslartQ%3D%3D
-
CS Le Lievre NM Le Douarin 1975 Mesenchymal derivatives of the neural crest: analysis of chimeric quail and chick embryos J Embryol Exp Morphol 34 125 154 1185098 1:STN:280:DyaE28%2FkslartQ%3D%3D
-
(1975)
J Embryol Exp Morphol
, vol.34
, pp. 125-154
-
-
Le Lievre, C.S.1
Le Douarin, N.M.2
-
37
-
-
0028899135
-
Early human T cell development: Analysis of the human thymus at the time of initial entry of hematopoietic stem cells into the fetal thymic microenvironment
-
7699329 10.1084/jem.181.4.1445 1:CAS:528:DyaK2MXkslWnt7k%3D
-
BF Haynes CS Heinly 1995 Early human T cell development: analysis of the human thymus at the time of initial entry of hematopoietic stem cells into the fetal thymic microenvironment J Exp Med 181 1445 1458 7699329 10.1084/jem.181.4.1445 1:CAS:528:DyaK2MXkslWnt7k%3D
-
(1995)
J Exp Med
, vol.181
, pp. 1445-1458
-
-
Haynes, B.F.1
Heinly, C.S.2
-
38
-
-
67651071559
-
Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: Possible implications for the pathophysiology of Omenn syndrome
-
19414857 10.1182/blood-2009-03-211029 1:CAS:528:DC%2BD1MXhtVOkurrE
-
PL Poliani F Facchetti M Ravanini AR Gennery A Villa CM Roifman LD Notarangelo 2009 Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndrome Blood 114 105 108 19414857 10.1182/blood-2009-03-211029 1:CAS:528:DC%2BD1MXhtVOkurrE
-
(2009)
Blood
, vol.114
, pp. 105-108
-
-
Poliani, P.L.1
Facchetti, F.2
Ravanini, M.3
Gennery, A.R.4
Villa, A.5
Roifman, C.M.6
Notarangelo, L.D.7
-
40
-
-
51349111243
-
The tumor necrosis factor family receptors RANK and CD40 cooperatively establish the thymic medullary microenvironment and self-tolerance
-
18799149 10.1016/j.immuni.2008.06.015 1:CAS:528:DC%2BD1cXhtF2jtLjK
-
T Akiyama Y Shimo H Yanai J Qin D Ohshima Y Maruyama Y Asaumi J Kitazawa H Takayanagi JM Penninger M Matsumoto T Nitta Y Takahama J Inoue 2008 The tumor necrosis factor family receptors RANK and CD40 cooperatively establish the thymic medullary microenvironment and self-tolerance Immunity 29 423 437 18799149 10.1016/j.immuni.2008.06.015 1:CAS:528:DC%2BD1cXhtF2jtLjK
-
(2008)
Immunity
, vol.29
, pp. 423-437
-
-
Akiyama, T.1
Shimo, Y.2
Yanai, H.3
Qin, J.4
Ohshima, D.5
Maruyama, Y.6
Asaumi, Y.7
Kitazawa, J.8
Takayanagi, H.9
Penninger, J.M.10
Matsumoto, M.11
Nitta, T.12
Takahama, Y.13
Inoue, J.14
-
41
-
-
0034662906
-
Normal thymic architecture and negative selection are associated with Aire expression, the gene defective in the autoimmune-polyendocrinopathy- candidiasis-ectodermal dystrophy (APECED)
-
S Zuklys G Balciunaite A Agarwal E Fasler-Kan E Palmer GA Holländer 2000 Normal thymic architecture and negative selection are associated with Aire expression, the gene defective in the autoimmune-polyendocrinopathy-candidiasis- ectodermal dystrophy (APECED) J Immunol 165 1976 1983 10925280 1:CAS:528:DC%2BD3cXls1KmsL8%3D (Pubitemid 30648747)
-
(2000)
Journal of Immunology
, vol.165
, Issue.4
, pp. 1976-1983
-
-
Zuklys, S.1
Balciunaite, G.2
Agarwal, A.3
Fasler-Kan, E.4
Palmer, E.5
Hollander, G.A.6
-
42
-
-
24144480562
-
+ regulatory T cells in human thymus
-
DOI 10.1038/nature03886
-
N Watanabe YH Wang HK Lee T Ito YH Wang W Cao YJ Liu 2005 Hassall's corpuscles instruct dendritic cells to induce CD4+ CD25+ regulatory T cells in human thymus Nature 436 1181 1185 16121185 10.1038/nature03886 1:CAS:528:DC%2BD2MXovVOgtrw%3D (Pubitemid 41232298)
-
(2005)
Nature
, vol.436
, Issue.7054
, pp. 1181-1185
-
-
Watanabe, N.1
Wang, Y.-H.2
Lee, H.K.3
Ito, T.4
Wang, Y.-H.5
Cao, W.6
Liu, Y.-J.7
-
43
-
-
0034672163
-
Similar pattern of thymic-dependent T-cell reconstitution in infants with severe combined immunodeficiency after human leukocyte antigen (HLA)-identical and HLA-nonidentical stem cell transplantation
-
11110711
-
SM Müller T Kohn AS Schulz KM Debatin W Friedrich 2000 Similar pattern of thymic-dependent T-cell reconstitution in infants with severe combined immunodeficiency after human leukocyte antigen (HLA)-identical and HLA-nonidentical stem cell transplantation Blood 96 4344 4349 11110711
-
(2000)
Blood
, vol.96
, pp. 4344-4349
-
-
Müller, S.M.1
Kohn, T.2
Schulz, A.S.3
Debatin, K.M.4
Friedrich, W.5
-
44
-
-
0346599403
-
An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
-
Finnish-German APECED Consortium 10.1038/ng1297-399
-
Finnish-German APECED Consortium 1997 An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains Nat Genet 17 399 403 10.1038/ng1297-399
-
(1997)
Nat Genet
, vol.17
, pp. 399-403
-
-
-
45
-
-
0035167967
-
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
-
DOI 10.1038/83713
-
CL Bennett J Christie F Ramsdell ME Brunkow PJ Ferguson L Whitesell TE Kelly FT Saulsbury PF Chance HD Ochs 2001 The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 Nat Genet 27 20 21 11137993 10.1038/83713 1:CAS:528: DC%2BD3MXis1yluw%3D%3D (Pubitemid 32044513)
-
(2001)
Nature Genetics
, vol.27
, Issue.1
, pp. 20-21
-
-
Bennett, C.L.1
Christie, J.2
Ramsdell, F.3
Brunkow, M.E.4
Ferguson, P.J.5
Whitesell, L.6
Kelly, T.E.7
Saulsbury, F.T.8
Chance, P.F.9
Ochs, H.D.10
-
46
-
-
70449484924
-
Thymus microenvironment in human primary immunodeficiency diseases
-
19841578 10.1097/ACI.0b013e3283327e5c
-
PL Poliani W Vermi F Facchetti 2009 Thymus microenvironment in human primary immunodeficiency diseases Curr Opin Allergy Clin Immunol 9 489 495 19841578 10.1097/ACI.0b013e3283327e5c
-
(2009)
Curr Opin Allergy Clin Immunol
, vol.9
, pp. 489-495
-
-
Poliani, P.L.1
Vermi, W.2
Facchetti, F.3
-
48
-
-
16944364802
-
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
-
AK Ryan JA Goodship DI Wilson N Philip A Levy H Seidel S Schuffenhauer H Oechsler B Belohradsky M Prieur A Aurias FL Raymond J Clayton-Smith E Hatchwell C McKeown FA Beemer B Dallapiccola G Novelli JA Hurst J Ignatius AJ Green RM Winter L Brueton K Brøndum-Nielsen PJ Scambler 1997 Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study J Med Genet 34 798 804 9350810 10.1136/jmg.34.10.798 1:STN:280:DyaK1c%2FhtVaqsQ%3D%3D (Pubitemid 27417432)
-
(1997)
Journal of Medical Genetics
, vol.34
, Issue.10
, pp. 798-804
-
-
Ryan, A.K.1
Goodship, J.A.2
Wilson, D.I.3
Philip, N.4
Levy, A.5
Seidel, H.6
Schuffenhauer, S.7
Oechsler, H.8
Belohradsky, B.9
Prieur, M.10
Aurias, A.11
Raymond, F.L.12
Clayton-Smith, J.13
Hatchwell, E.14
McKeown, C.15
Beemer, F.A.16
Dallapiccola, B.17
Novelli, G.18
Hurst, J.A.19
Ignatius, J.20
Green, A.J.21
Winter, R.M.22
Brueton, L.23
Brondum-Nielsen, K.24
Stewart, F.25
Van Essen, T.26
Patton, M.27
Paterson, J.28
Scambler, P.J.29
more..
-
49
-
-
0029838263
-
Repeated cytogenetic culture failure as an indicator of immunodeficiency [13]
-
JCK Barber JM Walker MR Barker AW McNinch RJ Hallett 1996 Repeated cytogenetic culture failure as an indicator of immunodeficiency Lancet 348 1518 8942803 10.1016/S0140-6736(05)65936-3 1:STN:280:DyaK2s%2FpvValsA%3D%3D (Pubitemid 26400263)
-
(1996)
Lancet
, vol.348
, Issue.9040
, pp. 1518
-
-
Barber, J.C.K.1
Walker, J.M.2
Barker, M.R.3
McNinch, A.W.4
Hallett, R.J.5
-
51
-
-
0035885937
-
Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: A study of 121 patients
-
11535520 10.1182/blood.V98.6.1847
-
SM Müller M Ege A Pottharst AS Schulz K Schwarz W Friedrich 2001 Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients Blood 98 1847 1851 11535520 10.1182/blood.V98.6.1847
-
(2001)
Blood
, vol.98
, pp. 1847-1851
-
-
Müller, S.M.1
Ege, M.2
Pottharst, A.3
Schulz, A.S.4
Schwarz, K.5
Friedrich, W.6
-
52
-
-
11144356685
-
Complete DiGeorge syndrome: Development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases
-
DOI 10.1016/j.jaci.2004.01.766
-
ML Markert MJ Alexieff J Li M Sarzotti DA Ozaki BH Devlin GD Sempowski ME Rhein P Szabolcs LP Hale RH Buckley KE Coyne HE Rice SM Mahaffey MA Skinner 2004 Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases J Allergy Clin Immunol 113 734 741 15100681 10.1016/j.jaci.2004.01.766 1:CAS:528:DC%2BD2cXjt1alt74%3D (Pubitemid 38530431)
-
(2004)
Journal of Allergy and Clinical Immunology
, vol.113
, Issue.4
, pp. 734-741
-
-
Markert, M.L.1
Alexieff, M.J.2
Li, J.3
Sarzotti, M.4
Ozaki, D.A.5
Devlin, B.H.6
Sempowski, G.D.7
Rhein, M.E.8
Szabolcs, P.9
Hale, L.P.10
Buckley, R.H.11
Coyne, K.E.12
Rice, H.E.13
Mahaffey, S.M.14
Skinner, M.A.15
-
53
-
-
77957714384
-
Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly
-
20530285 10.1182/blood-2010-03-275966 1:CAS:528:DC%2BC3cXhtlWrtLrJ
-
A Janda P Sedlacek M Hönig W Friedrich M Champagne T Matsumoto A Fischer B Neven A Contet D Bensoussan P Bordigoni D Loeb W Savage N Jabado FA Bonilla MA Slatter EG Davies AR Gennery 2010 Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly Blood 116 2229 2236 20530285 10.1182/blood-2010-03-275966 1:CAS:528:DC%2BC3cXhtlWrtLrJ
-
(2010)
Blood
, vol.116
, pp. 2229-2236
-
-
Janda, A.1
Sedlacek, P.2
Hönig, M.3
Friedrich, W.4
Champagne, M.5
Matsumoto, T.6
Fischer, A.7
Neven, B.8
Contet, A.9
Bensoussan, D.10
Bordigoni, P.11
Loeb, D.12
Savage, W.13
Jabado, N.14
Bonilla, F.A.15
Slatter, M.A.16
Davies, E.G.17
Gennery, A.R.18
-
54
-
-
70349606489
-
Immunologic reconstitution in 22q deletion (DiGeorge) syndrome
-
19238335 10.1007/s12026-009-8108-7
-
SA McGhee MG Lloret ER Stiehm 2009 Immunologic reconstitution in 22q deletion (DiGeorge) syndrome Immunol Res 45 37 45 19238335 10.1007/s12026-009- 8108-7
-
(2009)
Immunol Res
, vol.45
, pp. 37-45
-
-
McGhee, S.A.1
Lloret, M.G.2
Stiehm, E.R.3
-
55
-
-
77956395504
-
Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: Entering a new century, do we do better?
-
Inborn Errors Working Party of the European Group for Blood and Marrow Transplantation, European Society for Immunodeficiency
-
Gennery AR, Slatter MA, Grandin L, Taupin P, Cant AJ, Veys P, Amrolia PJ, Gaspar HB, Davies EG, Friedrich W, Hoenig M, Notarangelo LD, Mazzolari E, Porta F, Bredius RG, Lankester AC, Wulffraat NM, Seger R, Güngör T, Fasth A, Sedlacek P, Neven B, Blanche S, Fischer A, Cavazzana-Calvo M, Landais P, Inborn Errors Working Party of the European Group for Blood and Marrow Transplantation, European Society for Immunodeficiency (2010) Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: entering a new century, do we do better? J Allergy Clin Immunol 126, 602-10.e1-11
-
(2010)
J Allergy Clin Immunol
, vol.126
-
-
Gennery, A.R.1
Slatter, M.A.2
Grandin, L.3
Taupin, P.4
Cant, A.J.5
Veys, P.6
Amrolia, P.J.7
Gaspar, H.B.8
Davies, E.G.9
Friedrich, W.10
Hoenig, M.11
Notarangelo, L.D.12
Mazzolari, E.13
Porta, F.14
Bredius, R.G.15
Lankester, A.C.16
Wulffraat, N.M.17
Seger, R.18
Güngör, T.19
Fasth, A.20
Sedlacek, P.21
Neven, B.22
Blanche, S.23
Fischer, A.24
Cavazzana-Calvo, M.25
Landais, P.26
more..
-
56
-
-
65449161797
-
Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency
-
19168787 10.1182/blood-2008-09-177923 1:CAS:528:DC%2BD1MXlsVWrtrY%3D
-
B Neven S Leroy H Decaluwe F Le Deist C Picard D Moshous N Mahlaoui M Debré JL Casanova L Dal Cortivo Y Madec S Hacein-Bey-Abina G de Saint Basile JP de Villartay S Blanche M Cavazzana-Calvo A Fischer 2009 Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency Blood 113 4114 4124 19168787 10.1182/blood-2008-09-177923 1:CAS:528:DC%2BD1MXlsVWrtrY%3D
-
(2009)
Blood
, vol.113
, pp. 4114-4124
-
-
Neven, B.1
Leroy, S.2
Decaluwe, H.3
Le Deist, F.4
Picard, C.5
Moshous, D.6
Mahlaoui, N.7
Debré, M.8
Casanova, J.L.9
Dal Cortivo, L.10
Madec, Y.11
Hacein-Bey-Abina, S.12
De Saint Basile, G.13
De Villartay, J.P.14
Blanche, S.15
Cavazzana-Calvo, M.16
Fischer, A.17
-
57
-
-
0014406001
-
Foetal thymic transplant in a case of DiGeorge's syndrome
-
Cleveland WW, Fogel BJ, Brown WT, Kay HE (1968) Foetal thymic transplant in a case of DiGeorge's syndrome. Lancet (7580), 1211-1214
-
(1968)
Lancet
, Issue.7580
, pp. 1211-1214
-
-
Cleveland, W.W.1
Fogel, B.J.2
Brown, W.T.3
Kay, H.E.4
-
58
-
-
0014959576
-
Establishment of immunological competence in a child with congenital thymic aplasia by a graft of fetal thymus
-
August CS, Berkel AI, Levey RH, Rosen FS, Kay HE (1970). Establishment of immunological competence in a child with congenital thymic aplasia by a graft of fetal thymus. Lancet (7656):1080-1083
-
(1970)
Lancet
, Issue.7656
, pp. 1080-1083
-
-
August, C.S.1
Berkel, A.I.2
Levey, R.H.3
Rosen, F.S.4
Kay, H.E.5
-
59
-
-
0033554731
-
Transplantation of thymus tissue in complete DiGeorge syndrome
-
DOI 10.1056/NEJM199910143411603
-
ML Markert A Boeck LP Hale AL Kloster TM McLaughlin MN Batchvarova DC Douek RA Koup DD Kostyu FE Ward HE Rice SM Mahaffey SE Schiff RH Buckley BF Haynes 1999 Transplantation of thymus tissue in complete DiGeorge syndrome N Engl J Med 341 1180 1189 10523153 10.1056/NEJM199910143411603 1:STN:280:DyaK1MvjsFGnsA%3D%3D (Pubitemid 29480656)
-
(1999)
New England Journal of Medicine
, vol.341
, Issue.16
, pp. 1180-1189
-
-
Markert, M.L.1
Boeck, A.2
Hale, L.P.3
Kloster, A.L.4
McLaughlin, T.M.5
Batchvarova, M.N.6
Douek, D.C.7
Koup, R.A.8
Kostyu, D.D.9
Ward, F.E.10
Rice, H.E.11
Mahaffey, S.M.12
Schiff, S.E.13
Buckley, R.H.14
Haynes, B.F.15
-
60
-
-
77950627077
-
Thymus transplantation
-
20236866 10.1016/j.clim.2010.02.007 1:CAS:528:DC%2BC3cXkvFenu74%3D
-
ML Markert BH Devlin EA McCarthy 2010 Thymus transplantation Clin Immunol 135 236 246 20236866 10.1016/j.clim.2010.02.007 1:CAS:528:DC%2BC3cXkvFenu74%3D
-
(2010)
Clin Immunol
, vol.135
, pp. 236-246
-
-
Markert, M.L.1
Devlin, B.H.2
McCarthy, E.A.3
-
61
-
-
0041743085
-
Thymus transplantation in complete DiGeorge syndrome: Immunologic and safety evaluations in 12 patients
-
DOI 10.1182/blood-2002-08-2545
-
ML Markert M Sarzotti DA Ozaki GD Sempowski ME Rhein LP Hale F Le Deist MJ Alexieff J Li ER Hauser BF Haynes HE Rice MA Skinner SM Mahaffey J Jaggers LD Stein MR Mill 2003 Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients Blood 102 1121 1130 12702512 10.1182/blood-2002-08-2545 1:CAS:528:DC%2BD3sXlvFCmtLY%3D (Pubitemid 36917815)
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 1121-1130
-
-
Markert, M.L.1
Sarzotti, M.2
Ozaki, D.A.3
Sempowski, G.D.4
Rhein, M.E.5
Hale, L.P.6
Le Deist, F.7
Alexieff, M.J.8
Li, J.9
Hauser, E.R.10
Haynes, B.F.11
Rice, H.E.12
Skinner, M.A.13
Mahaffey, S.M.14
Jaggers, J.15
Stein, L.D.16
Mill, M.R.17
-
62
-
-
1942538141
-
Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome
-
DOI 10.1182/blood-2003-08-2984
-
ML Markert MJ Alexieff J Li M Sarzotti DA Ozaki BH Devlin DA Sedlak GD Sempowski LP Hale HE Rice SM Mahaffey MA Skinner 2004 Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome Blood 104 2574 2581 15100156 10.1182/blood-2003-08-2984 1:CAS:528:DC%2BD2cXovVegur8%3D (Pubitemid 39331863)
-
(2004)
Blood
, vol.104
, Issue.8
, pp. 2574-2581
-
-
Markert, M.L.1
Alexieff, M.J.2
Li, J.3
Sarzotti, M.4
Ozaki, D.A.5
Devlin, B.H.6
Sedlak, D.A.7
Sempowski, G.D.8
Hale, L.P.9
Rice, H.E.10
Mahaffey, S.M.11
Skinner, M.A.12
-
63
-
-
39149115649
-
Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly
-
18155964 10.1016/j.clim.2007.11.009 1:CAS:528:DC%2BD1cXitVWlu7k%3D
-
IK Chinn BH Devlin YJ Li ML Markert 2008 Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly Clin Immunol 126 277 281 18155964 10.1016/j.clim.2007.11.009 1:CAS:528:DC%2BD1cXitVWlu7k%3D
-
(2008)
Clin Immunol
, vol.126
, pp. 277-281
-
-
Chinn, I.K.1
Devlin, B.H.2
Li, Y.J.3
Markert, M.L.4
-
64
-
-
48349132851
-
Factors affecting success of thymus transplantation for complete DiGeorge anomaly
-
18557726 10.1111/j.1600-6143.2008.02301.x 1:STN:280: DC%2BD1crhtVGlsw%3D%3D
-
ML Markert BH Devlin IK Chinn EA McCarthy YJ Li 2008 Factors affecting success of thymus transplantation for complete DiGeorge anomaly Am J Transplant 8 1729 1736 18557726 10.1111/j.1600-6143.2008.02301.x 1:STN:280: DC%2BD1crhtVGlsw%3D%3D
-
(2008)
Am J Transplant
, vol.8
, pp. 1729-1736
-
-
Markert, M.L.1
Devlin, B.H.2
Chinn, I.K.3
McCarthy, E.A.4
Li, Y.J.5
-
65
-
-
0037383758
-
Aire regulates negative selection of organ-specific T cells
-
DOI 10.1038/ni906
-
A Liston S Lesage J Wilson L Peltonen CC Goodnow 2003 Aire regulates negative selection of organ-specific T cells Nat Immunol 4 350 354 12612579 10.1038/ni906 1:CAS:528:DC%2BD3sXitlyqs7w%3D (Pubitemid 36432317)
-
(2003)
Nature Immunology
, vol.4
, Issue.4
, pp. 350-354
-
-
Liston, A.1
Lesage, S.2
Wilson, J.3
Peltonen, L.4
Goodnow, C.C.5
-
66
-
-
23844558032
-
The cellular mechanism of Aire control of T cell tolerance
-
DOI 10.1016/j.immuni.2005.07.005, PII S1074761305002372
-
MS Anderson ES Venanzi Z Chen SP Berzins C Benoist D Mathis 2005 The cellular mechanism of Aire control of T cell tolerance Immunity 23 227 239 16111640 10.1016/j.immuni.2005.07.005 1:CAS:528:DC%2BD2MXpvVCnu7s%3D (Pubitemid 41169291)
-
(2005)
Immunity
, vol.23
, Issue.2
, pp. 227-239
-
-
Anderson, M.S.1
Venanzi, E.S.2
Chen, Z.3
Berzins, S.P.4
Benoist, C.5
Mathis, D.6
-
67
-
-
26644471257
-
An alternate pathway for CD4 T cell development: Thymocyte-expressed MHC class II selects a distinct T cell population
-
DOI 10.1016/j.immuni.2005.09.002, PII S107476130500275X
-
W Li MG Kim TS Gourley BP McCarthy DB Sant'Angelo CH Chang 2005 An alternate pathway for CD4 T cell development: thymocyte-expressed MHC class II selects a distinct T cell population Immunity 23 375 386 16226503 10.1016/j.immuni.2005.09.002 1:CAS:528:DC%2BD2MXht1Shs77K (Pubitemid 41443439)
-
(2005)
Immunity
, vol.23
, Issue.4
, pp. 375-386
-
-
Li, W.1
Kim, M.-G.2
Gourley, T.S.3
McCarthy, B.P.4
Sant'Angelo, D.B.5
Chang, C.-H.6
-
68
-
-
26644473419
-
Thymocyte-thymocyte interaction for efficient positive selection and maturation of CD4 T cells
-
DOI 10.1016/j.immuni.2005.09.005, PII S1074761305003006
-
EY Choi KC Jung HJ Park DH Chung JS Song SD Yang E Simpson SH Park 2005 Thymocyte-thymocyte interaction for efficient positive selection and maturation of CD4 T cells Immunity 23 387 396 16226504 10.1016/j.immuni.2005.09.005 1:CAS:528:DC%2BD2MXht1Shs77L (Pubitemid 41443440)
-
(2005)
Immunity
, vol.23
, Issue.4
, pp. 387-396
-
-
Eun, Y.C.1
Kyeong, C.J.2
Hyo, J.P.3
Doo, H.C.4
Jin, S.S.5
Seung, D.Y.6
Simpson, E.7
Seong, H.P.8
-
69
-
-
0029151334
-
Humoral immunity in DiGeorge syndrome
-
7636647 10.1016/S0022-3476(95)70300-4 1:STN:280:DyaK2MzmtlGqtw%3D%3D
-
AK Junker DA Driscoll 1995 Humoral immunity in DiGeorge syndrome J Pediatr 127 231 237 7636647 10.1016/S0022-3476(95)70300-4 1:STN:280: DyaK2MzmtlGqtw%3D%3D
-
(1995)
J Pediatr
, vol.127
, pp. 231-237
-
-
Junker, A.K.1
Driscoll, D.A.2
-
70
-
-
0032749270
-
Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
-
KE Sullivan D McDonald-McGinn DA Driscoll BS Emanuel EH Zackai AF Jawad 1999 Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/ velocardiofacial syndrome) Clin Diagn Lab Immunol 6 906 911 10548584 1:CAS:528:DyaK1MXnvVymsbw%3D (Pubitemid 29529986)
-
(1999)
Clinical and Diagnostic Laboratory Immunology
, vol.6
, Issue.6
, pp. 906-911
-
-
Sullivan, K.E.1
McDonald-McGinn, D.2
Driscoll, D.A.3
Emanuel, B.S.4
Zackai, E.H.5
Jawad, A.F.6
-
71
-
-
0035196580
-
Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
-
DOI 10.1067/mpd.2001.118534
-
AF Jawad DM McDonald-Mcginn E Zackai KE Sullivan 2001 Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/ velocardiofacial syndrome) J Pediatr 139 715 723 11713452 10.1067/mpd.2001. 118534 1:STN:280:DC%2BD3MnmslOhtw%3D%3D (Pubitemid 33097439)
-
(2001)
Journal of Pediatrics
, vol.139
, Issue.5
, pp. 715-723
-
-
Jawad, A.F.1
McDonald-McGinn, D.M.2
Zackai, E.3
Sullivan, K.E.4
-
72
-
-
21244439896
-
Post-natal ontogenesis of the T-cell receptor CD4 and CD8 Vβ repertoire and immune function in children with DiGeorge syndrome
-
DOI 10.1007/s10875-005-4085-3
-
C Cancrini ML Romiti A Finocchi S Di Cesare P Ciaffi C Capponi S Pahwa P Rossi 2005 Post-natal ontogenesis of the T-cell receptor CD4 and CD8 Vbeta repertoire and immune function in children with DiGeorge syndrome J Clin Immunol 25 265 274 15981092 10.1007/s10875-005-4085-3 1:CAS:528:DC%2BD2MXnsVehtb0%3D (Pubitemid 40884053)
-
(2005)
Journal of Clinical Immunology
, vol.25
, Issue.3
, pp. 265-274
-
-
Cancrini, C.1
Romiti, M.L.2
Finocchi, A.3
Di Cesare, S.4
Ciaffi, P.5
Capponi, C.6
Pahwa, S.7
Rossi, P.8
-
73
-
-
48349130692
-
Immunological defects in 22q11.2 deletion syndrome
-
18485468 10.1016/j.jaci.2008.03.033 1:CAS:528:DC%2BD1cXpsVGgsLw%3D
-
A McLean-Tooke D Barge GP Spickett AR Gennery 2008 Immunological defects in 22q11.2 deletion syndrome J Allergy Clin Immunol 122 362 367 18485468 10.1016/j.jaci.2008.03.033 1:CAS:528:DC%2BD1cXpsVGgsLw%3D
-
(2008)
J Allergy Clin Immunol
, vol.122
, pp. 362-367
-
-
McLean-Tooke, A.1
Barge, D.2
Spickett, G.P.3
Gennery, A.R.4
-
74
-
-
77953279171
-
Low thymic output in the 22q11.2 deletion syndrome measured by CCR9+ CD45RA+ T cell counts and T cell receptor rearrangement excision circles
-
20491792 1:CAS:528:DC%2BC3cXps1enurs%3D
-
K Lima TG Abrahamsen I Foelling S Natvig LP Ryder RW Olaussen 2010 Low thymic output in the 22q11.2 deletion syndrome measured by CCR9+ CD45RA+ T cell counts and T cell receptor rearrangement excision circles Clin Exp Immunol 161 98 107 20491792 1:CAS:528:DC%2BC3cXps1enurs%3D
-
(2010)
Clin Exp Immunol
, vol.161
, pp. 98-107
-
-
Lima, K.1
Abrahamsen, T.G.2
Foelling, I.3
Natvig, S.4
Ryder, L.P.5
Olaussen, R.W.6
-
75
-
-
1642581677
-
T-cell homeostasis in humans with thymic hypoplasia due to chromosome 22q11.2 deletion syndrome
-
DOI 10.1182/blood-2003-08-2824
-
LM Piliero AN Sanford DM McDonald-McGinn EH Zackai KE Sullivan 2004 T-cell homeostasis in humans with thymic hypoplasia due to chromosome 22q11.2 deletion syndrome Blood 103 1020 1025 14525774 10.1182/blood-2003-08-2824 1:CAS:528:DC%2BD2cXhtVaks78%3D (Pubitemid 38129565)
-
(2004)
Blood
, vol.103
, Issue.3
, pp. 1020-1025
-
-
Piliero, L.M.1
Sanford, A.N.2
McDonald-McGinn, D.M.3
Zackai, E.H.4
Sullivan, K.E.5
-
76
-
-
0038216872
-
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
-
DOI 10.1046/j.1365-2249.2003.02134.x
-
IM Pierdominic F Mazzetta E Caprini M Marziali MC Digilio B Marino A Aiuti F Amati G Russo G Novelli F Pandolfi G Luzi A Giovannetti 2003 Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Clin Exp Immunol 132 323 331 10.1046/j.1365-2249.2003.02134.x (Pubitemid 36560631)
-
(2003)
Clinical and Experimental Immunology
, vol.132
, Issue.2
, pp. 323-331
-
-
Pierdominici, M.1
Mazzetta, F.2
Caprini, E.3
Marziali, M.4
Digilio, M.C.5
Marino, B.6
Aiuti, A.7
Amati, F.8
Russo, G.9
Novelli, G.10
Pandolfi, F.11
Luzi, G.12
Giovannetti, A.13
-
77
-
-
20244377074
-
Early development of immunity in DiGeorge syndrome
-
Sedivá A, Bartůnková J, Zachová R, Poloucková A, Hrusák O, Janda A, Kocárek E, Novotná D, Novotná K, Klein T (2005) Early development of immunity in DiGeorge syndrome. Med Sci Monit 11: CR182-187
-
(2005)
Med Sci Monit
, vol.11
-
-
Sedivá, A.1
Bartůnková, J.2
Zachová, R.3
Poloucková, A.4
Hrusák, O.5
Janda, A.6
Kocárek, E.7
Novotná, D.8
Novotná, K.9
Klein, T.10
-
78
-
-
58149289799
-
Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome
-
19040613 10.1111/j.1365-2249.2008.03809.x 1:STN:280: DC%2BD1M%2Fls1ymsg%3D%3D
-
P Eberle C Berger S Junge S Dougoud EV Büchel M Riegel A Schinzel R Seger T Güngör 2009 Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome Clin Exp Immunol 155 189 198 19040613 10.1111/j.1365-2249.2008.03809.x 1:STN:280:DC%2BD1M%2Fls1ymsg%3D%3D
-
(2009)
Clin Exp Immunol
, vol.155
, pp. 189-198
-
-
Eberle, P.1
Berger, C.2
Junge, S.3
Dougoud, S.4
Büchel, E.V.5
Riegel, M.6
Schinzel, A.7
Seger, R.8
Güngör, T.9
-
79
-
-
77349097822
-
Association between hypoparathyroidism and defective T cell immunity in 22q11.2 deletion syndrome
-
20154038 10.1136/jcp.2009.072074 1:STN:280:DC%2BC3c7gsFChsg%3D%3D
-
A Herwadkar AR Gennery AS Moran MR Haeney PD Arkwright 2010 Association between hypoparathyroidism and defective T cell immunity in 22q11.2 deletion syndrome J Clin Pathol 63 151 155 20154038 10.1136/jcp.2009.072074 1:STN:280:DC%2BC3c7gsFChsg%3D%3D
-
(2010)
J Clin Pathol
, vol.63
, pp. 151-155
-
-
Herwadkar, A.1
Gennery, A.R.2
Moran, A.S.3
Haeney, M.R.4
Arkwright, P.D.5
-
81
-
-
33745611372
-
Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome)
-
DOI 10.1111/j.1399-3038.2006.00409.x
-
A Finocchi S Di Cesare ML Romiti C Capponi P Rossi R Carsetti C Cancrini 2006 Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome) Pediatr Allergy Immunol 17 382 388 16846458 10.1111/j.1399-3038.2006.00409.x 1:STN:280:DC%2BD28visFGntg%3D%3D (Pubitemid 43989962)
-
(2006)
Pediatric Allergy and Immunology
, vol.17
, Issue.5
, pp. 382-388
-
-
Finocchi, A.1
Di Cesare, S.2
Romiti, M.L.3
Capponi, C.4
Rossi, P.5
Carsetti, R.6
Cancrini, C.7
-
82
-
-
0026782016
-
Selective polysaccharide antibody deficiency in familial DiGeorge syndrome
-
1524280 1:STN:280:DyaK38zpvVWgtQ%3D%3D
-
MS Schubert RB Moss 1992 Selective polysaccharide antibody deficiency in familial DiGeorge syndrome Ann Allergy 69 231 238 1524280 1:STN:280: DyaK38zpvVWgtQ%3D%3D
-
(1992)
Ann Allergy
, vol.69
, pp. 231-238
-
-
Schubert, M.S.1
Moss, R.B.2
-
84
-
-
8644287589
-
Graves' disease in DiGeorge syndrome: Patient report with a review of endocrine autoimmunity associated with 22q11.2 deletion
-
Brown JJ, Datta V, Browning MJ, Swift PJF (2004) Graves' disease in Di George Syndrome: Patient report with a review of endocrine autoimmunity associated with 22q11.2 deletion. J Pediatr Endocrinol Metab 17: 1575-1579 (Pubitemid 39497012)
-
(2004)
Journal of Pediatric Endocrinology and Metabolism
, vol.17
, Issue.11
, pp. 1575-1579
-
-
Brown, J.J.1
Datta, V.2
Browning, M.J.3
Swift, P.G.F.4
-
86
-
-
0034790618
-
Juvenile idiopathic polyarticular arthritis and IgA deficiency in the 22q11 deletion syndrome
-
K Davies RE Stiehm P Woo KJ Murray 2001 Juvenile idiopathic polyarticular arthritis and IGA deficiency in the 22q11 deletion syndrome J Rheumatol 28 2326 2334 11669177 1:CAS:528:DC%2BD3MXnvVCisL4%3D (Pubitemid 32947884)
-
(2001)
Journal of Rheumatology
, vol.28
, Issue.10
, pp. 2326-2334
-
-
Davies, K.1
Stiehm, E.R.2
Woo, P.3
Murray, K.J.4
-
87
-
-
0027337952
-
Diversification, not use, of the immunoglobulin V(H) gene repertoire is restricted in DiGeorge syndrome
-
RN Haire RD Buell RT Litman Y Ohta SM Fu T Honjo F Matsuda M de la Morena J Carro RA Good GW Litman 1993 Diversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome J Exp Med 178 825 834 8350056 10.1084/jem.178.3.825 1:CAS:528:DyaK3sXlsFOqtrw%3D (Pubitemid 23260420)
-
(1993)
Journal of Experimental Medicine
, vol.178
, Issue.3
, pp. 825-834
-
-
Haire, R.N.1
Buell, R.D.2
Litman, R.T.3
Ohta, Y.4
Fu, S.M.5
Honjo, T.6
Matsuda, F.7
De La Morena, M.8
Carro, J.9
Good, R.A.10
Litman, G.W.11
-
88
-
-
0141940745
-
Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
-
14523220 10.1542/peds.112.4.e325
-
EE Perez A Bokszczanin D McDonald-McGinn EH Zackai KE Sullivan 2003 Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Pediatrics 112 e325 14523220 10.1542/peds.112.4.e325
-
(2003)
Pediatrics
, vol.112
, pp. 325
-
-
Perez, E.E.1
Bokszczanin, A.2
McDonald-Mcginn, D.3
Zackai, E.H.4
Sullivan, K.E.5
-
89
-
-
2942639783
-
Live viral vaccines in patients with partial DiGeorge syndrome: Clinical experience and cellular immunity
-
DOI 10.1016/j.clim.2004.02.008, PII S1521661604000567
-
EH Moylett AN Wasan LM Noroski WT Shearer 2004 Live viral vaccines in patients with partial DiGeorge syndrome: clinical experience and cellular immunity Clin Immunol 112 106 112 15207787 10.1016/j.clim.2004.02.008 1:CAS:528:DC%2BD2cXltVOisrk%3D (Pubitemid 38781063)
-
(2004)
Clinical Immunology
, vol.112
, Issue.1
, pp. 106-112
-
-
Moylett, E.H.1
Wasan, A.N.2
Noroski, L.M.3
Shearer, W.T.4
-
90
-
-
13444310815
-
Safety and immunogenicity of measles-mumps-rubella vaccine in children with congenital immunodeficiency (DiGeorge syndrome)
-
DOI 10.1016/j.vaccine.2004.10.005
-
C Azzari E Gambineri M Resti M Moriondo L Betti LRG Saldias AM Gelli A Vierucci 2005 Safety and immunogenicity of measles-mumps-rubella vaccine in children with congenital immunodeficiency (DiGeorge syndrome) Vaccine 23 1668 1671 15705470 10.1016/j.vaccine.2004.10.005 1:CAS:528:DC%2BD2MXhtlajs7c%3D (Pubitemid 40215699)
-
(2005)
Vaccine
, vol.23
, Issue.14
, pp. 1668-1671
-
-
Azzari, C.1
Gambineri, E.2
Resti, M.3
Moriondo, M.4
Betti, L.5
Saldias, L.R.6
Gelli, A.M.G.7
Vierucci, A.8
-
91
-
-
34249885380
-
Live viral vaccines in a DiGeorge syndrome patient
-
DOI 10.1136/adc.2006.097493
-
V Waters KS Peterson P LaRussa 2007 Live viral vaccines in a DiGeorge syndrome patient Arch Dis Child 92 519 520 16798784 10.1136/adc.2006.097493 1:STN:280:DC%2BD2szgt1Ohsw%3D%3D (Pubitemid 46867273)
-
(2007)
Archives of Disease in Childhood
, vol.92
, Issue.6
, pp. 519-520
-
-
Waters, V.1
Peterson, K.S.2
LaRussa, P.3
-
92
-
-
57149131812
-
Development of specific T-cell responses to Candida and tetanus antigens in partial DiGeorge syndrome
-
18789819 10.1016/j.jaci.2008.06.039 1:CAS:528:DC%2BD1cXhsV2ltr%2FE
-
CM Davis VS Kancherla A Reddy W Chan HW Yeh LM Noroski H Rosenblatt WT Shearer J Chinen 2008 Development of specific T-cell responses to Candida and tetanus antigens in partial DiGeorge syndrome J Allergy Clin Immunol 122 1194 1199 18789819 10.1016/j.jaci.2008.06.039 1:CAS:528:DC%2BD1cXhsV2ltr%2FE
-
(2008)
J Allergy Clin Immunol
, vol.122
, pp. 1194-1199
-
-
Davis, C.M.1
Kancherla, V.S.2
Reddy, A.3
Chan, W.4
Yeh, H.W.5
Noroski, L.M.6
Rosenblatt, H.7
Shearer, W.T.8
Chinen, J.9
-
93
-
-
77957783161
-
Safety and efficacy of measles, mumps, and rubella vaccine in patients with DiGeorge syndrome
-
20810153 10.1016/j.jaci.2010.07.018
-
N Al-Sukaiti B Reid S Lavi D Al-Zaharani A Atkinson CM Roifman E Grunebaum 2010 Safety and efficacy of measles, mumps, and rubella vaccine in patients with DiGeorge syndrome J Allergy Clin Immunol 126 868 869 20810153 10.1016/j.jaci.2010.07.018
-
(2010)
J Allergy Clin Immunol
, vol.126
, pp. 868-869
-
-
Al-Sukaiti, N.1
Reid, B.2
Lavi, S.3
Al-Zaharani, D.4
Atkinson, A.5
Roifman, C.M.6
Grunebaum, E.7
-
94
-
-
0037366965
-
Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: A case report
-
DOI 10.1080/0880010390158685
-
CP Kratz T Niehues S Lyding A Heusch G Janssen U Gobel 2003 Evans Syndrome in a patient with Chromosome 22q11.2 deletion syndrome: a case report Pediatr Hematol Oncol 20 167 172 12554529 10.1080/0880010390158685 1:CAS:528:DC%2BD3sXksVSkuw%3D%3D (Pubitemid 36222479)
-
(2003)
Pediatric Hematology and Oncology
, vol.20
, Issue.2
, pp. 167-172
-
-
Kratz, C.P.1
Niehues, T.2
Lyding, S.3
Heusch, A.4
Janssen, G.5
Gojbel, U.6
-
95
-
-
0029795561
-
Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: Coincidence or unusual complication?
-
DOI 10.1002/(SICI)1096-8628(19960906)64:4<546::AID-AJMG4>3.0.CO;2-N
-
SA Rasmussen CA Williams M Ayoube JW Sleasman BA Gray A Bent-Williams HJ Stalker T Zorir 1996 Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication Am J Med Genet 64 546 550 8870920 10.1002/(SICI)1096-8628(19960906)64:4<546::AID-AJMG4>3.0.CO;2-N 1:STN:280:DyaK2s%2FisVKqsQ%3D%3D (Pubitemid 26296100)
-
(1996)
American Journal of Medical Genetics
, vol.64
, Issue.4
, pp. 546-550
-
-
Rasmussen, S.A.1
Williams, C.A.2
Ayoub, E.M.3
Sleasman, J.W.4
Gray, B.A.5
Bent- Williams, A.6
Stalker, H.J.7
Zori, R.T.8
-
97
-
-
0031788096
-
Juvenile rheumatoid arthritis and del(22q11) syndrome: A non-random association
-
A Verloes C Curry M Jamar C Herens P O'Lague J Marks P Sarda P Blanchet 1998 Juvenile rheumatoid arthritis and del (22q11) syndrome: a non-random association J Med Genet 35 943 947 9832043 10.1136/jmg.35.11.943 1:STN:280:DyaK1M%2FkvVyrsQ%3D%3D (Pubitemid 28486624)
-
(1998)
Journal of Medical Genetics
, vol.35
, Issue.11
, pp. 943-947
-
-
Verloes, A.1
Curry, C.2
Jamar, M.3
Herens, C.4
O'Lague, P.5
Marks, J.6
Sarda, P.7
Blanchet, P.8
-
98
-
-
28444494764
-
Infections and autoimmune diseases
-
DOI 10.1016/j.jaut.2005.09.024, PII S0896841105001320
-
JF Bach 2005 Infections and autoimmune diseases J Autoimmun 25 Suppl 74 80 16278064 10.1016/j.jaut.2005.09.024 1:CAS:528:DC%2BD2MXht1Ghs7vM (Pubitemid 41728049)
-
(2005)
Journal of Autoimmunity
, vol.25
, Issue.SUPPL.
, pp. 74-80
-
-
Bach, J.-F.1
-
99
-
-
0038772004
-
Autoimmunity in Wiskott-Aldrich syndrome
-
DOI 10.1097/00002281-200307000-00012
-
SH Schurman F Candotti 2003 Autoimmunity in Wiskott-Aldrich syndrome Curr Opin Rheumatol 15 446 453 12819473 10.1097/00002281-200307000-00012 1:CAS:528:DC%2BD3sXltFKjsbw%3D (Pubitemid 36774257)
-
(2003)
Current Opinion in Rheumatology
, vol.15
, Issue.4
, pp. 446-453
-
-
Schurman, S.H.1
Candotti, F.2
-
100
-
-
77955272462
-
Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
-
20472505 10.1016/j.clim.2010.04.011 1:CAS:528:DC%2BC3cXpvFSru7k%3D
-
R Zemble E Luning Prak K McDonald D McDonald-McGinn E Zackai K Sullivan 2010 Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Clin Immunol 136 409 418 20472505 10.1016/j.clim.2010.04.011 1:CAS:528:DC%2BC3cXpvFSru7k%3D
-
(2010)
Clin Immunol
, vol.136
, pp. 409-418
-
-
Zemble, R.1
Luning Prak, E.2
McDonald, K.3
McDonald-Mcginn, D.4
Zackai, E.5
Sullivan, K.6
|