-
1
-
-
0030680207
-
Strike three for GLI3
-
Biesecker LG. Strike three for GLI3. Nat Genet. 1997 ; 17: 259-60
-
(1997)
Nat Genet
, vol.17
, pp. 259-260
-
-
Biesecker, L.G.1
-
2
-
-
70449627625
-
Ciliary biology: Understanding the cellular and genetic basis of human ciliopathies
-
Cardenas-Rodriguez M, Badano JL. Ciliary biology: understanding the cellular and genetic basis of human ciliopathies. Am J Med Genet (Part C). 2009 ; 151: 263-80
-
(2009)
Am J Med Genet (Part C)
, vol.151
, pp. 263-280
-
-
Cardenas-Rodriguez, M.1
Badano, J.L.2
-
3
-
-
3042756178
-
Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh
-
Chen Y, Knezeric V, Ervin V, Huston R, Ward Y, Macken S. Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh. Development. 2004 ; 131: 2339-47
-
(2004)
Development
, vol.131
, pp. 2339-2347
-
-
Chen, Y.1
Knezeric, V.2
Ervin, V.3
Huston, R.4
Ward, Y.5
Macken, S.6
-
4
-
-
77951101203
-
The primary cilium: A signaling center during vertebrate development
-
Goetz SC, Anderson KV. The primary cilium: a signaling center during vertebrate development. Nature Rev. 2010 ; 11: 331-44
-
(2010)
Nature Rev
, vol.11
, pp. 331-344
-
-
Goetz, S.C.1
Anderson, K.V.2
-
5
-
-
20144387269
-
Molecular and clinical analysis of Greig cephalopolysyndactyly and Pallister-Hall syndromes: Robust phenotype prediction from the type and position of GLI3 mutations
-
Johnston JJ, Olivos-Glander I, Killoran C, et al. Molecular and clinical analysis of Greig cephalopolysyndactyly and Pallister-Hall syndromes: Robust phenotype prediction from the type and position of GLI3 mutations. Am J Human Genet. 2005 ; 76: 609-22
-
(2005)
Am J Human Genet
, vol.76
, pp. 609-622
-
-
Johnston, J.J.1
Olivos-Glander, I.2
Killoran, C.3
-
6
-
-
79251474031
-
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations
-
Johnston JJ, Snapp JC, Turner JC, et al. Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations. Human Mutat. 2010 ; 31: 1142-54
-
(2010)
Human Mutat
, vol.31
, pp. 1142-1154
-
-
Johnston, J.J.1
Snapp, J.C.2
Turner, J.C.3
-
7
-
-
0032833002
-
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome
-
Kalff-Suske M, Wild A, Topp J, et al. Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome. Hum Mol Genet. 1999 ; 8: 1769-77
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1769-1777
-
-
Kalff-Suske, M.1
Wild, A.2
Topp, J.3
-
8
-
-
21344455343
-
Early development arrest of mammalian limbs lacking Hox A/Hox D gene function
-
Kmita M, Tarchini B, Zakany J, Logan M, Tabin CJ, Duboule D. Early development arrest of mammalian limbs lacking Hox A/Hox D gene function. Nature. 2005 ; 453: 1113-6
-
(2005)
Nature
, vol.453
, pp. 1113-1116
-
-
Kmita, M.1
Tarchini, B.2
Zakany, J.3
Logan, M.4
Tabin, C.J.5
Duboule, D.6
-
9
-
-
84862776586
-
Evolutionarily assembled cis-regulator module at a human ciliopathy locus
-
Lee JH, Silhavy JL, Lee JE, Al-Gazali L, Thomas S, Davis EE, et al. Evolutionarily assembled cis-regulator module at a human ciliopathy locus. Science. 2012 ; 335: 966-9
-
(2012)
Science
, vol.335
, pp. 966-969
-
-
Lee, J.H.1
Silhavy, J.L.2
Lee, J.E.3
Al-Gazali, L.4
Thomas, S.5
Davis, E.E.6
-
10
-
-
78649976507
-
Developmental biology and classification of congenital anomalies of the hand and upper extremity
-
Oberg KC, Feenstra JM, Manske PR, Tonkin MA. Developmental biology and classification of congenital anomalies of the hand and upper extremity. J Hand Surg Am. 2010 ; 35: 2066-76
-
(2010)
J Hand Surg Am
, vol.35
, pp. 2066-2076
-
-
Oberg, K.C.1
Feenstra, J.M.2
Manske, P.R.3
Tonkin, M.A.4
-
12
-
-
0033812186
-
Mutations in MKKS cause Bradet-Biedl syndrome
-
Slavotinek AM, Stone EM, Mykytyn K, et al. Mutations in MKKS cause Bradet-Biedl syndrome. Nat Genet. 2000 ; 26: 15-6
-
(2000)
Nat Genet
, vol.26
, pp. 15-16
-
-
Slavotinek, A.M.1
Stone, E.M.2
Mykytyn, K.3
|