-
1
-
-
17444451586
-
Behavioural phenotype of Bardet-Biedl syndrome
-
Barnett, S., Reilly, S., Carr, L., Ojo, I., Beales, P. L. and Charman, T. (2002). Behavioural phenotype of Bardet-Biedl syndrome. J. Med. Genet. 39, e76.
-
(2002)
J. Med. Genet.
, vol.39
-
-
Barnett, S.1
Reilly, S.2
Carr, L.3
Ojo, I.4
Beales, P.L.5
Charman, T.6
-
2
-
-
44449106038
-
Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors
-
Berbari, N. F., Johnson, A. D., Lewis, J. S., Askwith, C. C. and Mykytyn, K. (2008a). Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors. Mol. Biol. Cell 19, 1540-1547.
-
(2008)
Mol. Biol. Cell
, vol.19
, pp. 1540-1547
-
-
Berbari, N.F.1
Johnson, A.D.2
Lewis, J.S.3
Askwith, C.C.4
Mykytyn, K.5
-
3
-
-
41949116864
-
Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia
-
USA
-
Berbari, N. F., Lewis, J. S., Bishop, G. A., Askwith, C. C. and Mykytyn, K. (2008b). Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia. Proc. Natl. Acad. Sci. USA 105, 4242-4246.
-
(2008)
Proc. Natl. Acad. Sci.
, vol.105
, pp. 4242-4246
-
-
Berbari, N.F.1
Lewis, J.S.2
Bishop, G.A.3
Askwith, C.C.4
Mykytyn, K.5
-
4
-
-
3042738924
-
Loss of C.elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
-
Blacque, O. E., Reardon, M. J., Li, C., McCarthy, J., Mahjoub, M. R., Ansley, S. J., Badano, J. L., Mah, A. K., Beales, P. L., Davidson, W. S. et al. (2004). Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport. Genes Dev. 18, 1630-1642.
-
(2004)
Genes Dev.
, vol.18
, pp. 1630-1642
-
-
Blacque, O.E.1
Reardon, M.J.2
Li, C.3
McCarthy, J.4
Mahjoub, M.R.5
Ansley, S.J.6
Badano, J.L.7
Mah, A.K.8
Beales, P.L.9
Davidson, W.S.10
-
5
-
-
0028841278
-
Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci
-
Carmi, R., Elbedour, K., Stone, E. M. and Sheffield, V. C. (1995). Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci. Am. J. Med. Genet. 59, 199-203.
-
(1995)
Am. J. Med. Genet.
, vol.59
, pp. 199-203
-
-
Carmi, R.1
Elbedour, K.2
Stone, E.M.3
Sheffield, V.C.4
-
6
-
-
84870899794
-
Abnormal development of NG2+PDGFR-a+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model
-
Carter, C. S., Vogel, T. W., Zhang, Q., Seo, S., Swiderski, R. E., Moninger, T. O., Cassell, M. D., Thedens, D. R., Keppler-Noreuil, K. M., Nopoulos, P. et al. (2012). Abnormal development of NG2+PDGFR-a+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model. Nat. Med. 18, 1797-1804.
-
(2012)
Nat. Med.
, vol.18
, pp. 1797-1804
-
-
Carter, C.S.1
Vogel, T.W.2
Zhang, Q.3
Seo, S.4
Swiderski, R.E.5
Moninger, T.O.6
Cassell, M.D.7
Thedens, D.R.8
Keppler-Noreuil, K.M.9
Nopoulos, P.10
-
7
-
-
37649020306
-
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity
-
USA
-
Davis, R. E., Swiderski, R. E., Rahmouni, K., Nishimura, D. Y., Mullins, R. F., Agassandian, K., Philp, A. R., Searby, C. C., Andrews, M. P., Thompson, S. et al. (2007). A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity. Proc. Natl. Acad. Sci. USA 104, 19422-19427.
-
(2007)
Proc. Natl. Acad. Sci.
, vol.104
, pp. 19422-19427
-
-
Davis, R.E.1
Swiderski, R.E.2
Rahmouni, K.3
Nishimura, D.Y.4
Mullins, R.F.5
Agassandian, K.6
Philp, A.R.7
Searby, C.C.8
Andrews, M.P.9
Thompson, S.10
-
8
-
-
80051798889
-
Dopamine receptor 1 localizes to neuronal cilia in a dynamic process that requires the Bardet-Biedl syndrome proteins
-
Domire, J. S., Green, J. A., Lee, K. G., Johnson, A. D., Askwith, C. C. and Mykytyn, K. (2011). Dopamine receptor 1 localizes to neuronal cilia in a dynamic process that requires the Bardet-Biedl syndrome proteins. Cell. Mol. Life Sci. 68, 2951-2960. Eichers, E. R., Abd-El-Barr, M. M., Paylor, R., Lewis, R. A., Bi, W., Lin, X.,
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 2951-2960
-
-
Domire, J.S.1
Green, J.A.2
Lee, K.G.3
Johnson, A.D.4
Askwith, C.C.5
Mykytyn, K.6
-
9
-
-
33746959616
-
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity
-
Eichers, E. R., Abd-El-Barr, M. M., Paylor, R., Lewis, R. A., Bi, W., Lin, X., Meehan, T. P., Stockton, D. W., Wu, S. M., Lindsay, E. et al. (2006). Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity. Hum. Genet. 120, 211-226.
-
(2006)
Hum. Genet.
, vol.120
, pp. 211-226
-
-
Eichers, E.R.1
Abd-El-Barr, M.M.2
Paylor, R.3
Lewis, R.A.4
Bi, W.5
Lin, X.6
Meehan, T.P.7
Stockton, D.W.8
Wu, S.M.9
Lindsay, E.10
-
10
-
-
20944445215
-
Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome
-
Fath, M. A., Mullins, R. F., Searby, C., Nishimura, D. Y., Wei, J., Rahmouni, K., Davis, R. E., Tayeh, M. K., Andrews, M., Yang, B. et al. (2005). Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome. Hum. Mol. Genet. 14, 1109- 1118.
-
(2005)
Hum. Mol. Genet.
, vol.14
-
-
Fath, M.A.1
Mullins, R.F.2
Searby, C.3
Nishimura, D.Y.4
Wei, J.5
Rahmouni, K.6
Davis, R.E.7
Tayeh, M.K.8
Andrews, M.9
Yang, B.10
-
11
-
-
79952297519
-
Patients with Bardet-Biedl syndrome have hyperleptinemia suggestive of leptin resistance
-
Feuillan, P. P., Ng, D., Han, J. C., Sapp, J. C., Wetsch, K., Spaulding, E., Zheng, Y. C., Caruso, R. C., Brooks, B. P., Johnston, J. J. et al. (2011). Patients with Bardet-Biedl syndrome have hyperleptinemia suggestive of leptin resistance. J. Clin. Endocrinol. Metab. 96, E528-E535.
-
(2011)
J. Clin. Endocrinol. Metab.
, vol.96
-
-
Feuillan, P.P.1
Ng, D.2
Han, J.C.3
Sapp, J.C.4
Wetsch, K.5
Spaulding, E.6
Zheng, Y.C.7
Caruso, R.C.8
Brooks, B.P.9
Johnston, J.J.10
-
12
-
-
70349651962
-
The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development
-
Gray, R. S., Abitua, P. B., Wlodarczyk, B. J., Szabo-Rogers, H. L., Blanchard, O., Lee, I., Weiss, G. S., Liu, K. J., Marcotte, E. M., Wallingford, J. B. et al. (2009). The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development. Nat. Cell Biol. 11, 1225-1232.
-
(2009)
Nat. Cell Biol.
, vol.11
, pp. 1225-1232
-
-
Gray, R.S.1
Abitua, P.B.2
Wlodarczyk, B.J.3
Szabo-Rogers, H.L.4
Blanchard, O.5
Lee, I.6
Weiss, G.S.7
Liu, K.J.8
Marcotte, E.M.9
Wallingford, J.B.10
-
13
-
-
0033535628
-
Amygdaloid D1 dopamine receptor involvement in Pavlovian fear conditioning
-
Guarraci, F. A., Frohardt, R. J. and Kapp, B. S. (1999a). Amygdaloid D1 dopamine receptor involvement in Pavlovian fear conditioning. Brain Res. 827, 28-40.
-
(1999)
Brain Res.
, vol.827
, pp. 28-40
-
-
Guarraci, F.A.1
Frohardt, R.J.2
Kapp, B.S.3
-
14
-
-
0032780993
-
A functional role for dopamine transmission in the amygdala during conditioned fear
-
Guarraci, F. A., Frohardt, R. J., Young, S. L. and Kapp, B. S. (1999b). A functional role for dopamine transmission in the amygdala during conditioned fear. Ann. N. Y. Acad. Sci. 877, 732-736.
-
(1999)
Ann. N. Y. Acad. Sci.
, vol.877
, pp. 732-736
-
-
Guarraci, F.A.1
Frohardt, R.J.2
Young, S.L.3
Kapp, B.S.4
-
15
-
-
70349569932
-
Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking
-
Hsiao, Y. C., Tong, Z. J., Westfall, J. E., Ault, J. G., Page-McCaw, P. S. and Ferland, R. J. (2009). Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking. Hum. Mol. Genet. 18, 3926-3941.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3926-3941
-
-
Hsiao, Y.C.1
Tong, Z.J.2
Westfall, J.E.3
Ault, J.G.4
Page-McCaw, P.S.5
Ferland, R.J.6
-
16
-
-
77953879123
-
The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia
-
Jin, H., White, S. R., Shida, T., Schulz, S., Aguiar, M., Gygi, S. P., Bazan, J. F. and Nachury, M. V. (2010). The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia. Cell 141, 1208-1219.
-
(2010)
Cell
, vol.141
, pp. 1208-1219
-
-
Jin, H.1
White, S.R.2
Shida, T.3
Schulz, S.4
Aguiar, M.5
Gygi, S.P.6
Bazan, J.F.7
Nachury, M.V.8
-
17
-
-
4444254983
-
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse
-
Kulaga, H. M., Leitch, C. C., Eichers, E. R., Badano, J. L., Lesemann, A., Hoskins, B. E., Lupski, J. R., Beales, P. L., Reed, R. R. and Katsanis, N. (2004). Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nat. Genet. 36, 994-998.
-
(2004)
Nat. Genet.
, vol.36
, pp. 994-998
-
-
Kulaga, H.M.1
Leitch, C.C.2
Eichers, E.R.3
Badano, J.L.4
Lesemann, A.5
Hoskins, B.E.6
Lupski, J.R.7
Beales, P.L.8
Reed, R.R.9
Katsanis, N.10
-
18
-
-
76149101303
-
The Chlamydomonas reinhardtii BBSome is an IFT cargo required for export of specific signaling proteins from flagella
-
Lechtreck, K. F., Johnson, E. C., Sakai, T., Cochran, D., Ballif, B. A., Rush, J., Pazour, G. J., Ikebe, M. and Witman, G. B. (2009). The Chlamydomonas reinhardtii BBSome is an IFT cargo required for export of specific signaling proteins from flagella. J. Cell Biol. 187, 1117-1132.
-
(2009)
J. Cell Biol.
, vol.187
, pp. 1117-1132
-
-
Lechtreck, K.F.1
Johnson, E.C.2
Sakai, T.3
Cochran, D.4
Ballif, B.A.5
Rush, J.6
Pazour, G.J.7
Ikebe, M.8
Witman, G.B.9
-
19
-
-
84855179325
-
Hyperactive neuroendocrine secretion causes size, feeding, and metabolic defects of C. elegans Bardet-Biedl syndrome mutants
-
Lee, B. H., Liu, J., Wong, D., Srinivasan, S. and Ashrafi, K. (2011). Hyperactive neuroendocrine secretion causes size, feeding, and metabolic defects of C. elegans Bardet-Biedl syndrome mutants. PLoS Biol. 9, e1001219.
-
(2011)
PLoS Biol.
, vol.9
-
-
Lee, B.H.1
Liu, J.2
Wong, D.3
Srinivasan, S.4
Ashrafi, K.5
-
20
-
-
84868610108
-
T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection
-
Lee, R. J., Xiong, G., Kofonow, J. M., Chen, B., Lysenko, A., Jiang, P., Abraham, V., Doghramji, L., Adappa, N. D., Palmer, J. N. et al. (2012). T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection. J. Clin. Invest. 122, 4145-4159.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 4145-4159
-
-
Lee, R.J.1
Xiong, G.2
Kofonow, J.M.3
Chen, B.4
Lysenko, A.5
Jiang, P.6
Abraham, V.7
Doghramji, L.8
Adappa, N.D.9
Palmer, J.N.10
-
21
-
-
2942625562
-
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly
-
USA
-
Mykytyn, K., Mullins, R. F., Andrews, M., Chiang, A. P., Swiderski, R. E., Yang, B., Braun, T., Casavant, T., Stone, E. M. and Sheffield, V. C. (2004). Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly. Proc. Natl. Acad. Sci. USA 101, 8664-8669.
-
(2004)
Proc. Natl. Acad. Sci.
, vol.101
, pp. 8664-8669
-
-
Mykytyn, K.1
Mullins, R.F.2
Andrews, M.3
Chiang, A.P.4
Swiderski, R.E.5
Yang, B.6
Braun, T.7
Casavant, T.8
Stone, E.M.9
Sheffield, V.C.10
-
22
-
-
34250012834
-
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
-
Nachury, M. V., Loktev, A. V., Zhang, Q., Westlake, C. J., Peränen, J., Merdes, A., Slusarski, D. C., Scheller, R. H., Bazan, J. F., Sheffield, V. C. et al. (2007). A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. Cell 129, 1201-1213.
-
(2007)
Cell
, vol.129
, pp. 1201-1213
-
-
Nachury, M.V.1
Loktev, A.V.2
Zhang, Q.3
Westlake, C.J.4
Peränen, J.5
Merdes, A.6
Slusarski, D.C.7
Scheller, R.H.8
Bazan, J.F.9
Sheffield, V.C.10
-
23
-
-
9344261783
-
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin
-
USA
-
Nishimura, D. Y., Fath, M., Mullins, R. F., Searby, C., Andrews, M., Davis, R., Andorf, J. L., Mykytyn, K., Swiderski, R. E., Yang, B. et al. (2004). Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin. Proc. Natl. Acad. Sci. USA 101, 16588- 16593.
-
(2004)
Proc. Natl. Acad. Sci.
, vol.101
, pp. 16588-16593
-
-
Nishimura, D.Y.1
Fath, M.2
Mullins, R.F.3
Searby, C.4
Andrews, M.5
Davis, R.6
Andorf, J.L.7
Mykytyn, K.8
Swiderski, R.E.9
Yang, B.10
-
24
-
-
41849134729
-
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome
-
Rahmouni, K., Fath, M. A., Seo, S., Thedens, D. R., Berry, C. J., Weiss, R., Nishimura, D. Y. and Sheffield, V. C. (2008). Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome. J. Clin. Invest. 118, 1458-1467.
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 1458-1467
-
-
Rahmouni, K.1
Fath, M.A.2
Seo, S.3
Thedens, D.R.4
Berry, C.J.5
Weiss, R.6
Nishimura, D.Y.7
Sheffield, V.C.8
-
25
-
-
79960937678
-
The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disorders
-
Sattar, S. and Gleeson, J. G. (2011). The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disorders. Dev. Med. Child Neurol. 53, 793-798.
-
(2011)
Dev. Med. Child Neurol.
, vol.53
, pp. 793-798
-
-
Sattar, S.1
Gleeson, J.G.2
-
26
-
-
63149175815
-
Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling
-
Seo, S., Guo, D. F., Bugge, K., Morgan, D. A., Rahmouni, K. and Sheffield, V. C. (2009). Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling.Hum. Mol. Genet. 18, 1323-1331.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1323-1331
-
-
Seo, S.1
Guo, D.F.2
Bugge, K.3
Morgan, D.A.4
Rahmouni, K.5
Sheffield, V.C.6
-
27
-
-
76549121983
-
BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly
-
USA
-
Seo, S., Baye, L. M., Schulz, N. P., Beck, J. S., Zhang, Q., Slusarski, D. C. and Sheffield, V. C. (2010). BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly. Proc. Natl. Acad. Sci. USA 107, 1488-1493.
-
(2010)
Proc. Natl. Acad. Sci.
, vol.107
, pp. 1488-1493
-
-
Seo, S.1
Baye, L.M.2
Schulz, N.P.3
Beck, J.S.4
Zhang, Q.5
Slusarski, D.C.6
Sheffield, V.C.7
-
28
-
-
69549084858
-
Motile cilia of human airway epithelia are chemosensory
-
Shah, A. S., Ben-Shahar, Y., Moninger, T. O., Kline, J. N. and Welsh, M. J. (2009). Motile cilia of human airway epithelia are chemosensory. Science 325, 1131-1134.
-
(2009)
Science
, vol.325
, pp. 1131-1134
-
-
Shah, A.S.1
Ben-Shahar, Y.2
Moninger, T.O.3
Kline, J.N.4
Welsh, M.J.5
-
29
-
-
34548059278
-
Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage
-
Swiderski, R. E., Nishimura, D. Y., Mullins, R. F., Olvera, M. A., Ross, J. L., Huang, J., Stone, E. M. and Sheffield, V. C. (2007). Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage. Invest. Ophthalmol. Vis. Sci. 48, 3329-3340.
-
(2007)
Invest. Ophthalmol. Vis. Sci.
, vol.48
, pp. 3329-3340
-
-
Swiderski, R.E.1
Nishimura, D.Y.2
Mullins, R.F.3
Olvera, M.A.4
Ross, J.L.5
Huang, J.6
Stone, E.M.7
Sheffield, V.C.8
-
30
-
-
84865803552
-
The BBSome controls IFT assembly and turnaround in cilia
-
Wei, Q., Zhang, Y., Li, Y., Zhang, Q., Ling, K. and Hu, J. (2012). The BBSome controls IFT assembly and turnaround in cilia. Nat. Cell Biol. 14, 950-957.
-
(2012)
Nat. Cell Biol.
, vol.14
, pp. 950-957
-
-
Wei, Q.1
Zhang, Y.2
Li, Y.3
Zhang, Q.4
Ling, K.5
Hu, J.6
-
31
-
-
84867237029
-
Association of a bitter taste receptor mutation with Balkan Endemic Nephropathy (BEN)
-
Wooding, S. P., Atanasova, S., Gunn, H. C., Staneva, R., Dimova, I. and Toncheva, D. (2012). Association of a bitter taste receptor mutation with Balkan Endemic Nephropathy (BEN). BMC Med. Genet. 13, 96.
-
(2012)
BMC Med. Genet.
, vol.13
, pp. 96
-
-
Wooding, S.P.1
Atanasova, S.2
Gunn, H.C.3
Staneva, R.4
Dimova, I.5
Toncheva, D.6
-
32
-
-
33144456230
-
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function
-
Yen, H. J., Tayeh, M. K., Mullins, R. F., Stone, E. M., Sheffield, V. C. and Slusarski, D. C. (2006). Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function. Hum. Mol. Genet. 15, 667-677.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 667-677
-
-
Yen, H.J.1
Tayeh, M.K.2
Mullins, R.F.3
Stone, E.M.4
Sheffield, V.C.5
Slusarski, D.C.6
-
33
-
-
84862908687
-
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes
-
USA
-
Zhang, Q., Nishimura, D., Seo, S., Vogel, T., Morgan, D. A., Searby, C., Bugge, K., Stone, E. M., Rahmouni, K. and Sheffield, V. C. (2011). Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes. Proc. Natl. Acad. Sci. USA 108, 20678-20683.
-
(2011)
Proc. Natl. Acad. Sci.
, vol.108
, pp. 20678-20683
-
-
Zhang, Q.1
Nishimura, D.2
Seo, S.3
Vogel, T.4
Morgan, D.A.5
Searby, C.6
Bugge, K.7
Stone, E.M.8
Rahmouni, K.9
Sheffield, V.C.10
-
34
-
-
84859219770
-
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes
-
Zhang, Q., Seo, S., Bugge, K., Stone, E. M. and Sheffield, V. C. (2012a). BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes. Hum. Mol. Genet. 21, 1945-1953.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1945-1953
-
-
Zhang, Q.1
Seo, S.2
Bugge, K.3
Stone, E.M.4
Sheffield, V.C.5
-
35
-
-
84862004139
-
Intrinsic proteinprotein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome
-
Zhang, Q., Yu, D., Seo, S., Stone, E. M. and Sheffield, V. C. (2012b). Intrinsic proteinprotein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome. J. Biol. Chem. 287, 20625-20635.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 20625-20635
-
-
Zhang, Q.1
Yu, D.2
Seo, S.3
Stone, E.M.4
Sheffield, V.C.5
|