-
1
-
-
0031003272
-
SOX9 directly regulates the type-II collagen gene
-
Bell D.M., Leung K.K., Wheatley S.C., Ng L.J., Zhou S., Ling K.W., Sham M.H., Koopman P., Tam P.P., Cheah K.S. SOX9 directly regulates the type-II collagen gene. Nat. Genet. 16:1997;174-178.
-
(1997)
Nat. Genet.
, vol.16
, pp. 174-178
-
-
Bell, D.M.1
Leung, K.K.2
Wheatley, S.C.3
Ng, L.J.4
Zhou, S.5
Ling, K.W.6
Sham, M.H.7
Koopman, P.8
Tam, P.P.9
Cheah, K.S.10
-
2
-
-
0345711458
-
Sox9 is required for cartilage formation
-
Bi W., Deng J.M., Zhang Z., Behringer R.R., de Crombrugghe B. Sox9 is required for cartilage formation. Nat. Genet. 22:1999;85-89.
-
(1999)
Nat. Genet.
, vol.22
, pp. 85-89
-
-
Bi, W.1
Deng, J.M.2
Zhang, Z.3
Behringer, R.R.4
De Crombrugghe, B.5
-
3
-
-
0034669139
-
Phylogeny of the Sox family of developmental transcription factors based on sequence and structural indicators
-
Bowles J., Schepers G., Koopman P. Phylogeny of the Sox family of developmental transcription factors based on sequence and structural indicators. Dev. Biol. 227:2000;239-255.
-
(2000)
Dev. Biol.
, vol.227
, pp. 239-255
-
-
Bowles, J.1
Schepers, G.2
Koopman, P.3
-
4
-
-
0035182190
-
The transcription factor Sox10 is a key regulator of peripheral glial development
-
Britsch S., Goerich D.E., Riethmacher D., Peirano R.I., Rossner M., Nave K.A., Birchmeier C., Wegner M. The transcription factor Sox10 is a key regulator of peripheral glial development. Genes. Dev. 15:2001;66-78.
-
(2001)
Genes. Dev.
, vol.15
, pp. 66-78
-
-
Britsch, S.1
Goerich, D.E.2
Riethmacher, D.3
Peirano, R.I.4
Rossner, M.5
Nave, K.A.6
Birchmeier, C.7
Wegner, M.8
-
5
-
-
0032938895
-
Regulation and role of Sox9 in cartilage formation
-
Healy C., Uwanogho D., Sharpe P.T. Regulation and role of Sox9 in cartilage formation. Dev. Dyn. 215:1999;69-78.
-
(1999)
Dev. Dyn.
, vol.215
, pp. 69-78
-
-
Healy, C.1
Uwanogho, D.2
Sharpe, P.T.3
-
6
-
-
0020615253
-
The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al. 1971
-
Houston C.S., Opitz J.M., Spranger J.W., Macpherson R.I., Reed M.H., Gilbert E.F., Herrmann J., Schinzel A. The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al. 1971. Am. J. Med. Genet. 15:1983;3-28.
-
(1983)
Am. J. Med. Genet.
, vol.15
, pp. 3-28
-
-
Houston, C.S.1
Opitz, J.M.2
Spranger, J.W.3
Macpherson, R.I.4
Reed, M.H.5
Gilbert, E.F.6
Herrmann, J.7
Schinzel, A.8
-
7
-
-
0031903569
-
Involvement of Sox1, 2 and 3 in the early and subsequent molecular events of lens induction
-
Kamachi Y., Uchikawa M., Collignon J., Lovell-Badge R., Kondoh H. Involvement of Sox1, 2 and 3 in the early and subsequent molecular events of lens induction. Development. 125:1998;2521-2532.
-
(1998)
Development
, vol.125
, pp. 2521-2532
-
-
Kamachi, Y.1
Uchikawa, M.2
Collignon, J.3
Lovell-Badge, R.4
Kondoh, H.5
-
8
-
-
0036545995
-
Expression of human SOX7 in normal tissues and tumors
-
Katoh M. Expression of human SOX7 in normal tissues and tumors. Int. J. Mol. Med. 9:2002;363-368.
-
(2002)
Int. J. Mol. Med.
, vol.9
, pp. 363-368
-
-
Katoh, M.1
-
9
-
-
0035167769
-
Impaired autonomic control of the heart by Sox10 mutation
-
Korsch E., Steinkuhle J., Massin M., Lyonnet S., Touraine R.L. Impaired autonomic control of the heart by Sox10 mutation. Eur. J. Pediatr. 160:2001;68-69.
-
(2001)
Eur. J. Pediatr.
, vol.160
, pp. 68-69
-
-
Korsch, E.1
Steinkuhle, J.2
Massin, M.3
Lyonnet, S.4
Touraine, R.L.5
-
10
-
-
0032189223
-
A new long form of Sox 5 (L-Sox5), Sox 6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene
-
Lefebvre V., Li P., de Crombrugghe B. A new long form of Sox 5 (L-Sox5), Sox 6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene. EMBO J. 17:1998;5718-5733.
-
(1998)
EMBO J.
, vol.17
, pp. 5718-5733
-
-
Lefebvre, V.1
Li, P.2
De Crombrugghe, B.3
-
11
-
-
0031104994
-
SOX9 binds DNA,activates transcription, and coexpresses with type II collagen during chondrogenesis of the mouse
-
Ng L.-J., Wheatley S., Muscat G.E.O., Conway-Campbell J., Bowles J., Wright E., Bell D.M., Tam P.P.L., Cheah K.S.E., Koopman P. SOX9 binds DNA,activates transcription, and coexpresses with type II collagen during chondrogenesis of the mouse. Dev. Biol. 183:1997;108-121.
-
(1997)
Dev. Biol.
, vol.183
, pp. 108-121
-
-
Ng, L.-J.1
Wheatley, S.2
Muscat, G.E.O.3
Conway-Campbell, J.4
Bowles, J.5
Wright, E.6
Bell, D.M.7
Tam, P.P.L.8
Cheah, K.S.E.9
Koopman, P.10
-
12
-
-
0034069877
-
Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice
-
Pennisi D., Gardner J., Chambers D., Hosking B., Peters J., Muscat G., Abbott C., Koopman P. Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice. Nat. Genet. 24:2000;434-437.
-
(2000)
Nat. Genet.
, vol.24
, pp. 434-437
-
-
Pennisi, D.1
Gardner, J.2
Chambers, D.3
Hosking, B.4
Peters, J.5
Muscat, G.6
Abbott, C.7
Koopman, P.8
-
13
-
-
0033995606
-
The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome
-
Pfeifer D., Poulat F., Holinski-Feder E., Kooy F., Scherer G. The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome. Genomics. 63:2000;108-116.
-
(2000)
Genomics
, vol.63
, pp. 108-116
-
-
Pfeifer, D.1
Poulat, F.2
Holinski-Feder, E.3
Kooy, F.4
Scherer, G.5
-
14
-
-
17344366171
-
Sox10 mutations in patients with Waardenburg-Hirschsprung disease
-
Pingault V., Bondurand N., Kuhlbrodt K., Goerich D.E., Prehu M.O., Puliti A., Herbarth B., Hermans-Borgmeyer I., Legius E., Matthijs G., Amiel J., Lyonnet S., Ceccherini I., Romeo G., Smith J.C., Read A.P., Wegner M., Goossens M. Sox10 mutations in patients with Waardenburg-Hirschsprung disease. Nat. Genet. 18:1998;171-173.
-
(1998)
Nat. Genet.
, vol.18
, pp. 171-173
-
-
Pingault, V.1
Bondurand, N.2
Kuhlbrodt, K.3
Goerich, D.E.4
Prehu, M.O.5
Puliti, A.6
Herbarth, B.7
Hermans-Borgmeyer, I.8
Legius, E.9
Matthijs, G.10
Amiel, J.11
Lyonnet, S.12
Ceccherini, I.13
Romeo, G.14
Smith, J.C.15
Read, A.P.16
Wegner, M.17
Goossens, M.18
-
15
-
-
0034886920
-
A novel sox gene, 226D7, acts downstream of Nodal signaling to specify endoderm precursors in zebrafish
-
Sakaguchi T., Kuroiwa A., Takeda H. A novel sox gene, 226D7, acts downstream of Nodal signaling to specify endoderm precursors in zebrafish. Mech. Dev. 107:2001;25-38.
-
(2001)
Mech. Dev.
, vol.107
, pp. 25-38
-
-
Sakaguchi, T.1
Kuroiwa, A.2
Takeda, H.3
-
16
-
-
0034654222
-
Cloning and characterisation of the Sry-related transcription factor gene Sox8
-
Schepers G.E., Bullejos M., Hosking B.M., Koopman P. Cloning and characterisation of the Sry-related transcription factor gene Sox8. Nucleic Acids Res. 28:2000;1473-1480.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 1473-1480
-
-
Schepers, G.E.1
Bullejos, M.2
Hosking, B.M.3
Koopman, P.4
-
17
-
-
15844362094
-
Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4
-
Schilham M.W., Oosterwegel M.A., Moerer P., Ya J., de Boer P.A., van de Wetering M., Verbeek S., Lamers W.H., Kruisbeek A.M., Cumano A., Clevers H. Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4. Nature. 380:1996;711-714.
-
(1996)
Nature
, vol.380
, pp. 711-714
-
-
Schilham, M.W.1
Oosterwegel, M.A.2
Moerer, P.3
Ya, J.4
De Boer, P.A.5
Van de Wetering, M.6
Verbeek, S.7
Lamers, W.H.8
Kruisbeek, A.M.9
Cumano, A.10
Clevers, H.11
-
18
-
-
0034646703
-
Sox9 enhances aggrecan gene promoter/enhancer activity and is up-regulated by retinoic acid in a cartilage-derived cell line, TC6
-
Sekiya I., Tsuji K., Koopman P., Watanabe H., Yamada Y., Shinomiya K., Nifuji A., Noda M. Sox9 enhances aggrecan gene promoter/enhancer activity and is up-regulated by retinoic acid in a cartilage-derived cell line, TC6. J. Biol. Chem. 275:2000;10738-10744.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 10738-10744
-
-
Sekiya, I.1
Tsuji, K.2
Koopman, P.3
Watanabe, H.4
Yamada, Y.5
Shinomiya, K.6
Nifuji, A.7
Noda, M.8
-
19
-
-
0034807930
-
Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8
-
Sock E., Schmidt K., Hermanns-Borgmeyer I., Bosl M.R., Wegner M. Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8. Mol. Cell. Biol. 21:2001;6951-6959.
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 6951-6959
-
-
Sock, E.1
Schmidt, K.2
Hermanns-Borgmeyer, I.3
Bosl, M.R.4
Wegner, M.5
-
20
-
-
0027959045
-
Type II collagen is transiently expressed during avian cardiac valve morphogenesis
-
Swiderski R.E., Daniels K.J., Jensen K.L., Solursh M. Type II collagen is transiently expressed during avian cardiac valve morphogenesis. Dev. Dyn. 200:1994;294-304.
-
(1994)
Dev. Dyn.
, vol.200
, pp. 294-304
-
-
Swiderski, R.E.1
Daniels, K.J.2
Jensen, K.L.3
Solursh, M.4
-
21
-
-
0028589588
-
Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene Sox9
-
Wagner T., Wirth J., Meyer J., Zabel B., Held M., Zimmer J., Pasantes J., Bricarelli F.D., Keutel J., Hustert E., Wolf U., Tommerup N., Schempp W., Scherer G. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene Sox9. Cell. 79:1994;1111-1120.
-
(1994)
Cell
, vol.79
, pp. 1111-1120
-
-
Wagner, T.1
Wirth, J.2
Meyer, J.3
Zabel, B.4
Held, M.5
Zimmer, J.6
Pasantes, J.7
Bricarelli, F.D.8
Keutel, J.9
Hustert, E.10
Wolf, U.11
Tommerup, N.12
Schempp, W.13
Scherer, G.14
-
22
-
-
0033485842
-
Distinct spatial and temporal distributions of aggrecan and versican in the embryonic chick heart
-
Zanin M.K., Bundy J., Ernst H., Wessels A., Conway S.J., Hoffman S. Distinct spatial and temporal distributions of aggrecan and versican in the embryonic chick heart. Anat. Rec. 256:1999;366-380.
-
(1999)
Anat. Rec.
, vol.256
, pp. 366-380
-
-
Zanin, M.K.1
Bundy, J.2
Ernst, H.3
Wessels, A.4
Conway, S.J.5
Hoffman, S.6
|