-
1
-
-
0030962307
-
Gene expression profiles in normal and cancer cells
-
Zhang L., Zhou W., Velculescu V.E., Kern S.E., Hruban R.H., Hamilton S.R., Vogelstein B., and Kinzler K.W. Gene expression profiles in normal and cancer cells. Science 276 (1997) 1268-1272
-
(1997)
Science
, vol.276
, pp. 1268-1272
-
-
Zhang, L.1
Zhou, W.2
Velculescu, V.E.3
Kern, S.E.4
Hruban, R.H.5
Hamilton, S.R.6
Vogelstein, B.7
Kinzler, K.W.8
-
2
-
-
0345051044
-
Normalization and subtraction: two approaches to facilitate gene discovery
-
Bonaldo M.F., Lennon G., and Soares M.B. Normalization and subtraction: two approaches to facilitate gene discovery. Genome Res. 6 (1996) 791-806
-
(1996)
Genome Res.
, vol.6
, pp. 791-806
-
-
Bonaldo, M.F.1
Lennon, G.2
Soares, M.B.3
-
3
-
-
23644460630
-
Tag-based approaches for transcriptome research and genome annotation
-
Harbers M., and Carninci P. Tag-based approaches for transcriptome research and genome annotation. Nat. Methods 2 (2005) 495-502
-
(2005)
Nat. Methods
, vol.2
, pp. 495-502
-
-
Harbers, M.1
Carninci, P.2
-
5
-
-
0034130561
-
Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays
-
Brenner S., Johnson M., Bridgham J., Golda G., Lloyd D.H., Johnson D., Luo S., McCurdy S., Foy M., Ewan M., Roth R., George D., Eletr S., Albrecht G., Vermaas E., Williams S.R., Moon K., Burcham T., Pallas M., DuBridge R.B., Kirchner J., Fearon K., Mao J., and Corcoran K. Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays. Nat. Biotechnol. 18 (2000) 630-634
-
(2000)
Nat. Biotechnol.
, vol.18
, pp. 630-634
-
-
Brenner, S.1
Johnson, M.2
Bridgham, J.3
Golda, G.4
Lloyd, D.H.5
Johnson, D.6
Luo, S.7
McCurdy, S.8
Foy, M.9
Ewan, M.10
Roth, R.11
George, D.12
Eletr, S.13
Albrecht, G.14
Vermaas, E.15
Williams, S.R.16
Moon, K.17
Burcham, T.18
Pallas, M.19
DuBridge, R.B.20
Kirchner, J.21
Fearon, K.22
Mao, J.23
Corcoran, K.24
more..
-
6
-
-
2942553957
-
The use of MPSS for whole-genome transcriptional analysis in Arabidopsis
-
Meyers B.C., Tej S.S., Vu T.H., Haudenschild C.D., Agrawal V., Edberg S.B., Ghazal H., and Decola S. The use of MPSS for whole-genome transcriptional analysis in Arabidopsis. Genome Res. 14 (2004) 1641-1653
-
(2004)
Genome Res.
, vol.14
, pp. 1641-1653
-
-
Meyers, B.C.1
Tej, S.S.2
Vu, T.H.3
Haudenschild, C.D.4
Agrawal, V.5
Edberg, S.B.6
Ghazal, H.7
Decola, S.8
-
7
-
-
4544319518
-
MPSS profiling of human embryonic stem cells
-
Brandenberger R., Khrebtukova I., Thies R.S., Miura T., Jingli C., Puri R., Vasicek T., Lebkowski J., and Rao M. MPSS profiling of human embryonic stem cells. BMC Dev. Biol. 4 (2004) 10
-
(2004)
BMC Dev. Biol.
, vol.4
, pp. 10
-
-
Brandenberger, R.1
Khrebtukova, I.2
Thies, R.S.3
Miura, T.4
Jingli, C.5
Puri, R.6
Vasicek, T.7
Lebkowski, J.8
Rao, M.9
-
8
-
-
13444304325
-
NCBI GEO: mining millions of expression profiles-Database and tools
-
Barrett T., Suzek T.O., Troup D.B., Wilhite S.E., Ngau W.-C., Ledoux P., Rudnev D., Lash A.E., Fujibuchi W., and Edgar R. NCBI GEO: mining millions of expression profiles-Database and tools. Nucleic Acids Res. 33 (2005) D562-D566
-
(2005)
Nucleic Acids Res.
, vol.33
-
-
Barrett, T.1
Suzek, T.O.2
Troup, D.B.3
Wilhite, S.E.4
Ngau, W.-C.5
Ledoux, P.6
Rudnev, D.7
Lash, A.E.8
Fujibuchi, W.9
Edgar, R.10
-
9
-
-
0036081355
-
Gene expression omnibus: NCBI gene expression and hybridization array data repository
-
Edgar R., Domrachev M., and Lash A.E. Gene expression omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 30 (2002) 207-210
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 207-210
-
-
Edgar, R.1
Domrachev, M.2
Lash, A.E.3
-
10
-
-
22244475458
-
An atlas of human gene expression from massively parallel signature sequencing (MPSS)
-
Jongeneel C.V., Delorenzi M., Iseli C., Zhou D., Haudenschild C.D., Khrebtukova I., Kuznetsov D., Stevenson B.J., Strausberg R.L., Simpson A.J.G., and Vasicek T.J. An atlas of human gene expression from massively parallel signature sequencing (MPSS). Genome Res. 15 (2005) 1007-1014
-
(2005)
Genome Res.
, vol.15
, pp. 1007-1014
-
-
Jongeneel, C.V.1
Delorenzi, M.2
Iseli, C.3
Zhou, D.4
Haudenschild, C.D.5
Khrebtukova, I.6
Kuznetsov, D.7
Stevenson, B.J.8
Strausberg, R.L.9
Simpson, A.J.G.10
Vasicek, T.J.11
-
11
-
-
24644472515
-
Antisense transcription in the mammalian transcriptome
-
Katayama S., Tomaru Y., Kasukawa T., Waki K., Nakanishi M., Nakamura M., Nishida H., Yap C.C., Suzuki M., Kawai J., Suzuki H., Carninci P., Hayashizaki Y., Wells C., Frith M., Ravasi T., Pang K.C., Hallinan J., Mattick J., Hume D.A., Lipovich L., Batalov S., Engstrom P.G., Mizuno Y., Faghihi M.A., Sandelin A., Chalk A.M., Mottagui-Tabar S., Liang Z., Lenhard B., and Wahlestedt C. Antisense transcription in the mammalian transcriptome. Science 309 (2005) 1564-1566
-
(2005)
Science
, vol.309
, pp. 1564-1566
-
-
Katayama, S.1
Tomaru, Y.2
Kasukawa, T.3
Waki, K.4
Nakanishi, M.5
Nakamura, M.6
Nishida, H.7
Yap, C.C.8
Suzuki, M.9
Kawai, J.10
Suzuki, H.11
Carninci, P.12
Hayashizaki, Y.13
Wells, C.14
Frith, M.15
Ravasi, T.16
Pang, K.C.17
Hallinan, J.18
Mattick, J.19
Hume, D.A.20
Lipovich, L.21
Batalov, S.22
Engstrom, P.G.23
Mizuno, Y.24
Faghihi, M.A.25
Sandelin, A.26
Chalk, A.M.27
Mottagui-Tabar, S.28
Liang, Z.29
Lenhard, B.30
Wahlestedt, C.31
more..
-
14
-
-
0038581890
-
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
-
Tufarelli C., Stanley J.A., Garrick D., Sharpe J.A., Ayyub H., Wood W.G., and Higgs D.R. Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease. Nat. Genet. 34 (2003) 157-165
-
(2003)
Nat. Genet.
, vol.34
, pp. 157-165
-
-
Tufarelli, C.1
Stanley, J.A.2
Garrick, D.3
Sharpe, J.A.4
Ayyub, H.5
Wood, W.G.6
Higgs, D.R.7
-
15
-
-
12244275645
-
Widespread occurrence of antisense transcription in the human genome
-
Yelin R., Dahary D., Sorek R., Levanon E.Y., Goldstein O., Shoshan A., Diber A., Biton S., Tamir Y., Khosravi R., Nemzer S., Pinner E., Walach S., Bernstein J., Savitsky K., and Rotman G. Widespread occurrence of antisense transcription in the human genome. Nat. Biotechnol. 21 (2003) 379-386
-
(2003)
Nat. Biotechnol.
, vol.21
, pp. 379-386
-
-
Yelin, R.1
Dahary, D.2
Sorek, R.3
Levanon, E.Y.4
Goldstein, O.5
Shoshan, A.6
Diber, A.7
Biton, S.8
Tamir, Y.9
Khosravi, R.10
Nemzer, S.11
Pinner, E.12
Walach, S.13
Bernstein, J.14
Savitsky, K.15
Rotman, G.16
-
16
-
-
2642566736
-
Identification of unique transcripts from a mouse full-length, subtracted inner ear cDNA library
-
Beisel K.W., Shiraki T., Morris K.A., Pompeia C., Kachar B., Arakawa T., Bono H., Kawai J., Hayashizaki Y., and Carninci P. Identification of unique transcripts from a mouse full-length, subtracted inner ear cDNA library. Genomics 83 (2004) 1012-1023
-
(2004)
Genomics
, vol.83
, pp. 1012-1023
-
-
Beisel, K.W.1
Shiraki, T.2
Morris, K.A.3
Pompeia, C.4
Kachar, B.5
Arakawa, T.6
Bono, H.7
Kawai, J.8
Hayashizaki, Y.9
Carninci, P.10
-
17
-
-
0345133276
-
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle
-
Belyantseva I.A., Boger E.T., and Friedman T.B. Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 13958-13963
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 13958-13963
-
-
Belyantseva, I.A.1
Boger, E.T.2
Friedman, T.B.3
-
18
-
-
0036201664
-
Prestin, the motor protein of outer hair cells
-
Zheng J., Madison L.D., Oliver D., Fakler B., and Dallos P. Prestin, the motor protein of outer hair cells. Audiol. Neurootol. 7 (2002) 9-12
-
(2002)
Audiol. Neurootol.
, vol.7
, pp. 9-12
-
-
Zheng, J.1
Madison, L.D.2
Oliver, D.3
Fakler, B.4
Dallos, P.5
-
19
-
-
0032729835
-
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2
-
Liang Y., Wang A., Belyantseva I.A., Anderson D.W., Probst F.J., Barber T.D., Miller W., Touchman J.W., Jin L., Sullivan S.L., Sellers J.R., Camper S.A., Lloyd R.V., Kachar B., Friedman T.B., and Fridell R.A. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics 61 (1999) 243-258
-
(1999)
Genomics
, vol.61
, pp. 243-258
-
-
Liang, Y.1
Wang, A.2
Belyantseva, I.A.3
Anderson, D.W.4
Probst, F.J.5
Barber, T.D.6
Miller, W.7
Touchman, J.W.8
Jin, L.9
Sullivan, S.L.10
Sellers, J.R.11
Camper, S.A.12
Lloyd, R.V.13
Kachar, B.14
Friedman, T.B.15
Fridell, R.A.16
-
20
-
-
0034794785
-
Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumors
-
Lloyd R.V., Vidal S., Jin L., Zhang S., Kovacs K., Horvath E., Scheithauer B.W., Boger E.T.A., Fridell R.A., and Friedman T.B. Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumors. Am. J. Pathol. 159 (2001) 1375-1382
-
(2001)
Am. J. Pathol.
, vol.159
, pp. 1375-1382
-
-
Lloyd, R.V.1
Vidal, S.2
Jin, L.3
Zhang, S.4
Kovacs, K.5
Horvath, E.6
Scheithauer, B.W.7
Boger, E.T.A.8
Fridell, R.A.9
Friedman, T.B.10
-
21
-
-
0034636553
-
Prestin is the motor protein of cochlear outer hair cells
-
Zheng J., Shen W., He D.Z., Long K.B., Madison L.D., and Dallos P. Prestin is the motor protein of cochlear outer hair cells. Nature 405 (2000) 149-155
-
(2000)
Nature
, vol.405
, pp. 149-155
-
-
Zheng, J.1
Shen, W.2
He, D.Z.3
Long, K.B.4
Madison, L.D.5
Dallos, P.6
-
22
-
-
20444390168
-
Otolith matrix proteins OMP-1 and Otolin-1 are necessary for normal otolith growth and their correct anchoring onto the sensory maculae
-
Murayama E., Herbomel P., Kawakami A., Takeda H., and Nagasawa H. Otolith matrix proteins OMP-1 and Otolin-1 are necessary for normal otolith growth and their correct anchoring onto the sensory maculae. Mech. Dev. 122 (2005) 791-803
-
(2005)
Mech. Dev.
, vol.122
, pp. 791-803
-
-
Murayama, E.1
Herbomel, P.2
Kawakami, A.3
Takeda, H.4
Nagasawa, H.5
-
23
-
-
0036164231
-
Fish otolith contains a unique structural protein, otolin-1
-
Murayama E., Takagi Y., Ohira T., Davis J.G., Greene M.I., and Nagasawa H. Fish otolith contains a unique structural protein, otolin-1. Eur. J. Biochem. 269 (2002) 688-696
-
(2002)
Eur. J. Biochem.
, vol.269
, pp. 688-696
-
-
Murayama, E.1
Takagi, Y.2
Ohira, T.3
Davis, J.G.4
Greene, M.I.5
Nagasawa, H.6
-
24
-
-
21844457412
-
UMODL1/Olfactorin is an extracellular membrane-bound molecule with a restricted spatial expression in olfactory and vomeronasal neurons
-
Di Schiavi E., Riano E., Heye B., Bazzicalupo P., and Rugarli E.I. UMODL1/Olfactorin is an extracellular membrane-bound molecule with a restricted spatial expression in olfactory and vomeronasal neurons. Eur. J. Neurosci. 21 (2005) 3291-3300
-
(2005)
Eur. J. Neurosci.
, vol.21
, pp. 3291-3300
-
-
Di Schiavi, E.1
Riano, E.2
Heye, B.3
Bazzicalupo, P.4
Rugarli, E.I.5
-
25
-
-
2942604996
-
Initial characterization of an uromodulin-like 1 gene on human chromosome 21q22.3
-
Shibuya K., Nagamine K., Okui M., Ohsawa Y., Asakawa S., Minoshima S., Hase T., Kudoh J., and Shimizu N. Initial characterization of an uromodulin-like 1 gene on human chromosome 21q22.3. Biochem. Biophys. Res. Commun. 319 (2004) 1181-1189
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.319
, pp. 1181-1189
-
-
Shibuya, K.1
Nagamine, K.2
Okui, M.3
Ohsawa, Y.4
Asakawa, S.5
Minoshima, S.6
Hase, T.7
Kudoh, J.8
Shimizu, N.9
-
26
-
-
0033846745
-
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9
-
Yasunaga S., Grati M., Chardenoux S., Smith T.N., Friedman T.B., Lalwani A.K., Wilcox E.R., and Petit C. OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. Am. J. Hum. Genet. 67 (2000) 591-600
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 591-600
-
-
Yasunaga, S.1
Grati, M.2
Chardenoux, S.3
Smith, T.N.4
Friedman, T.B.5
Lalwani, A.K.6
Wilcox, E.R.7
Petit, C.8
-
27
-
-
0029938771
-
Development of the auditory receptors of the rat: a SEM study
-
Zine A., and Romand R. Development of the auditory receptors of the rat: a SEM study. Brain Res. 721 (1996) 49-58
-
(1996)
Brain Res.
, vol.721
, pp. 49-58
-
-
Zine, A.1
Romand, R.2
-
28
-
-
0141765843
-
Developmental acquisition of sensory transduction in hair cells of the mouse inner ear
-
Geleoc G.S., and Holt J.R. Developmental acquisition of sensory transduction in hair cells of the mouse inner ear. Nat. Neurosci. 6 (2003) 1019-1020
-
(2003)
Nat. Neurosci.
, vol.6
, pp. 1019-1020
-
-
Geleoc, G.S.1
Holt, J.R.2
-
29
-
-
0037447251
-
Comprehensive sampling of gene expression in human cell lines with massively parallel signature sequencing
-
Jongeneel C.V., Iseli C., Stevenson B.J., Riggins G.J., Lal A., Mackay A., Harris R.A., O'Hare M.J., Neville A.M., Simpson A.J.G., and Strausberg R.L. Comprehensive sampling of gene expression in human cell lines with massively parallel signature sequencing. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 4702-4705
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 4702-4705
-
-
Jongeneel, C.V.1
Iseli, C.2
Stevenson, B.J.3
Riggins, G.J.4
Lal, A.5
Mackay, A.6
Harris, R.A.7
O'Hare, M.J.8
Neville, A.M.9
Simpson, A.J.G.10
Strausberg, R.L.11
-
30
-
-
0042968976
-
The power of the 3′ UTR: translational control and development
-
Kuersten S., and Goodwin E.B. The power of the 3′ UTR: translational control and development. Nat. Rev. Genet. 4 (2003) 626-637
-
(2003)
Nat. Rev. Genet.
, vol.4
, pp. 626-637
-
-
Kuersten, S.1
Goodwin, E.B.2
-
31
-
-
18344415808
-
Distinguishing regulatory DNA from neutral sites
-
Elnitski L., Hardison R.C., Li J., Yang S., Kolbe D., Eswara P., O'Connor M.J., Schwartz S., Miller W., and Chiaromonte F. Distinguishing regulatory DNA from neutral sites. Genome Res. 13 (2003) 64-72
-
(2003)
Genome Res.
, vol.13
, pp. 64-72
-
-
Elnitski, L.1
Hardison, R.C.2
Li, J.3
Yang, S.4
Kolbe, D.5
Eswara, P.6
O'Connor, M.J.7
Schwartz, S.8
Miller, W.9
Chiaromonte, F.10
-
32
-
-
34548093996
-
A catalog of stability-associated sequence elements in 3′ UTRs of yeast mRNAs
-
Shalgi R., Lapidot M., Shamir R., and Pilpel Y. A catalog of stability-associated sequence elements in 3′ UTRs of yeast mRNAs. Genome Biol. 6 (2005) R86
-
(2005)
Genome Biol.
, vol.6
-
-
Shalgi, R.1
Lapidot, M.2
Shamir, R.3
Pilpel, Y.4
-
33
-
-
28944439309
-
Animal microRNAs confer robustness to gene expression and have a significant impact on 3′UTR evolution
-
Stark A., Brennecke J., Bushati N., Russell R.B., and Cohen S.M. Animal microRNAs confer robustness to gene expression and have a significant impact on 3′UTR evolution. Cell 123 (2005) 1133-1146
-
(2005)
Cell
, vol.123
, pp. 1133-1146
-
-
Stark, A.1
Brennecke, J.2
Bushati, N.3
Russell, R.B.4
Cohen, S.M.5
-
34
-
-
15244358503
-
Systematic discovery of regulatory motifs in human promoters and 3′ UTRs by comparison of several mammals
-
Xie X., Lu J., Kulbokas E.J., Golub T.R., Mootha V., Lindblad-Toh K., Lander E.S., and Kellis M. Systematic discovery of regulatory motifs in human promoters and 3′ UTRs by comparison of several mammals. Nature 434 (2005) 338-345
-
(2005)
Nature
, vol.434
, pp. 338-345
-
-
Xie, X.1
Lu, J.2
Kulbokas, E.J.3
Golub, T.R.4
Mootha, V.5
Lindblad-Toh, K.6
Lander, E.S.7
Kellis, M.8
-
35
-
-
18444408090
-
Long-range heterogeneity at the 3′ ends of human mRNAs
-
Iseli C., Stevenson B.J., de Souza S.J., Samaia H.B., Camargo A.A., Buetow K.H., Strausberg R.L., Simpson A.J., Bucher P., and Jongeneel C.V. Long-range heterogeneity at the 3′ ends of human mRNAs. Genome Res. 12 (2002) 1068-1074
-
(2002)
Genome Res.
, vol.12
, pp. 1068-1074
-
-
Iseli, C.1
Stevenson, B.J.2
de Souza, S.J.3
Samaia, H.B.4
Camargo, A.A.5
Buetow, K.H.6
Strausberg, R.L.7
Simpson, A.J.8
Bucher, P.9
Jongeneel, C.V.10
-
36
-
-
21244501527
-
-
Toriello H., Reardon W., and Gorlin R. (Eds), Oxford Univ. Press, Oxford
-
In: Toriello H., Reardon W., and Gorlin R. (Eds). Hereditary Hearing Loss and Its Syndromes (2004), Oxford Univ. Press, Oxford
-
(2004)
Hereditary Hearing Loss and Its Syndromes
-
-
-
37
-
-
33845982830
-
Genetic hearing loss associated with eye disorders
-
Toriello H., Reardon W., and Gorlin R. (Eds), Oxford Univ. Press, Oxford
-
Kimberling W. Genetic hearing loss associated with eye disorders. In: Toriello H., Reardon W., and Gorlin R. (Eds). Hereditary Hearing Loss and Its Syndromes (2004), Oxford Univ. Press, Oxford 126-165
-
(2004)
Hereditary Hearing Loss and Its Syndromes
, pp. 126-165
-
-
Kimberling, W.1
-
38
-
-
0033616582
-
Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase
-
Chen C.-K., Burns M.E., Spencer M., Niemi G.A., Chen J., Hurley J.B., Baylor D.A., and Simon M.I. Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 3718-3722
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 3718-3722
-
-
Chen, C.-K.1
Burns, M.E.2
Spencer, M.3
Niemi, G.A.4
Chen, J.5
Hurley, J.B.6
Baylor, D.A.7
Simon, M.I.8
-
39
-
-
0031797078
-
A new allelic series for the underwhite gene on mouse chromosome 15
-
Sweet H.O., Brilliant M.H., Cook S.A., Johnson K.R., and Davisson M.T. A new allelic series for the underwhite gene on mouse chromosome 15. J. Hered. 89 (1998) 546-551
-
(1998)
J. Hered.
, vol.89
, pp. 546-551
-
-
Sweet, H.O.1
Brilliant, M.H.2
Cook, S.A.3
Johnson, K.R.4
Davisson, M.T.5
-
40
-
-
0028657579
-
Information coding in the olfactory system: evidence for a stereotyped and highly organized epitope map in the olfactory bulb
-
Ressler K.J., Sullivan S.L., and Buck L.B. Information coding in the olfactory system: evidence for a stereotyped and highly organized epitope map in the olfactory bulb. Cell 79 (1994) 1245-1255
-
(1994)
Cell
, vol.79
, pp. 1245-1255
-
-
Ressler, K.J.1
Sullivan, S.L.2
Buck, L.B.3
-
41
-
-
11844301284
-
Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin
-
Delprat B., Ruel J., Guitton M.J., Hamard G., Lenoir M., Pujol R., Puel J.-L., Brabet P., and Hamel C.P. Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin. Mol. Cell. Biol. 25 (2005) 847-853
-
(2005)
Mol. Cell. Biol.
, vol.25
, pp. 847-853
-
-
Delprat, B.1
Ruel, J.2
Guitton, M.J.3
Hamard, G.4
Lenoir, M.5
Pujol, R.6
Puel, J.-L.7
Brabet, P.8
Hamel, C.P.9
-
42
-
-
17344364928
-
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
-
Verhoeven K., Van Laer L., Kirschhofer K., Legan P.K., Hughes D.C., Schatteman I., Verstreken M., Van Hauwe P., Coucke P., Chen A., Smith R.J., Somers T., Offeciers F.E., Van de Heyning P., Richardson G.P., Wachtler F., Kimberling W.J., Willems P.J., Govaerts P.J., and Van Camp G. Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nat. Genet. 19 (1998) 60-62
-
(1998)
Nat. Genet.
, vol.19
, pp. 60-62
-
-
Verhoeven, K.1
Van Laer, L.2
Kirschhofer, K.3
Legan, P.K.4
Hughes, D.C.5
Schatteman, I.6
Verstreken, M.7
Van Hauwe, P.8
Coucke, P.9
Chen, A.10
Smith, R.J.11
Somers, T.12
Offeciers, F.E.13
Van de Heyning, P.14
Richardson, G.P.15
Wachtler, F.16
Kimberling, W.J.17
Willems, P.J.18
Govaerts, P.J.19
Van Camp, G.20
more..
-
43
-
-
0032977996
-
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21
-
Mustapha M., Weil D., Chardenoux S., Elias S., El-Zir E., Beckmann J.S., Loiselet J., and Petit C. An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum. Mol. Genet. 8 (1999) 409-412
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 409-412
-
-
Mustapha, M.1
Weil, D.2
Chardenoux, S.3
Elias, S.4
El-Zir, E.5
Beckmann, J.S.6
Loiselet, J.7
Petit, C.8
-
44
-
-
0033951215
-
Targeted disruption of otog results in deafness and severe imbalance
-
Simmler M.C., Cohen-Salmon M., El-Amraoui A., Guillaud L., Benichou J.C., Petit C., and Panthier J.J. Targeted disruption of otog results in deafness and severe imbalance. Nat. Genet. 24 (2000) 139-143
-
(2000)
Nat. Genet.
, vol.24
, pp. 139-143
-
-
Simmler, M.C.1
Cohen-Salmon, M.2
El-Amraoui, A.3
Guillaud, L.4
Benichou, J.C.5
Petit, C.6
Panthier, J.J.7
-
45
-
-
19444375650
-
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients
-
Asamura K., Abe S., Fukuoka H., Nakamura Y., and Usami S. Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients. Auris Nasus Larynx 32 (2005) 113-117
-
(2005)
Auris Nasus Larynx
, vol.32
, pp. 113-117
-
-
Asamura, K.1
Abe, S.2
Fukuoka, H.3
Nakamura, Y.4
Usami, S.5
-
46
-
-
13844269032
-
Type IX collagen knock-out mouse shows progressive hearing loss
-
Suzuki N., Asamura K., Kikuchi Y., Takumi Y., Abe S., Imamura Y., Hayashi T., Aszodi A., Fassler R., and Usami S. Type IX collagen knock-out mouse shows progressive hearing loss. Neurosci. Res. 51 (2005) 293-298
-
(2005)
Neurosci. Res.
, vol.51
, pp. 293-298
-
-
Suzuki, N.1
Asamura, K.2
Kikuchi, Y.3
Takumi, Y.4
Abe, S.5
Imamura, Y.6
Hayashi, T.7
Aszodi, A.8
Fassler, R.9
Usami, S.10
-
47
-
-
0032430262
-
Otoconin-90, the mammalian otoconial matrix protein, contains two domains of homology to secretory phospholipase A2
-
Wang Y., Kowalski P.E., Thalmann I., Ornitz D.M., Mager D.L., and Thalmann R. Otoconin-90, the mammalian otoconial matrix protein, contains two domains of homology to secretory phospholipase A2. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 15345-15350
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 15345-15350
-
-
Wang, Y.1
Kowalski, P.E.2
Thalmann, I.3
Ornitz, D.M.4
Mager, D.L.5
Thalmann, R.6
-
48
-
-
0030889074
-
The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system
-
Legan P.K., Rau A., Keen J.N., and Richardson G.P. The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system. J. Biol. Chem. 272 (1997) 8791-8801
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 8791-8801
-
-
Legan, P.K.1
Rau, A.2
Keen, J.N.3
Richardson, G.P.4
-
49
-
-
4244083959
-
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22
-
Zwaenepoel I., Mustapha M., Leibovici M., Verpy E., Goodyear R., Liu X.Z., Nouaille S., Nance W.E., Kanaan M., Avraham K.B., Tekaia F., Loiselet J., Lathrop M., Richardson G., and Petit C. Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 6240-6245
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 6240-6245
-
-
Zwaenepoel, I.1
Mustapha, M.2
Leibovici, M.3
Verpy, E.4
Goodyear, R.5
Liu, X.Z.6
Nouaille, S.7
Nance, W.E.8
Kanaan, M.9
Avraham, K.B.10
Tekaia, F.11
Loiselet, J.12
Lathrop, M.13
Richardson, G.14
Petit, C.15
|