-
1
-
-
0028897860
-
Isolation of cDNAs that are differentially expressed between androgen-dependent and androgen-independent prostate carcinoma cells using differential display PCR
-
Blok, L.J., Kumar, M.V., Tindall, D.J., 1995. Isolation of cDNAs that are differentially expressed between androgen-dependent and androgen-independent prostate carcinoma cells using differential display PCR. Prostate 26, 213-224.
-
(1995)
Prostate
, vol.26
, pp. 213-224
-
-
Blok, L.J.1
Kumar, M.V.2
Tindall, D.J.3
-
2
-
-
0018639079
-
Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
-
Chirgwin, J.M., Przybyla, A.E., MacDonald, R.J., Rutter, W.J., 1979. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18, 5294-5299.
-
(1979)
Biochemistry
, vol.18
, pp. 5294-5299
-
-
Chirgwin, J.M.1
Przybyla, A.E.2
MacDonald, R.J.3
Rutter, W.J.4
-
3
-
-
0030839583
-
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21
-
Greinwald Jr., J.H., Scott, D.A., Marietta, J.R., Carmi, R., Manaligod, J., Ramesh, A., Zbar, R.I.S., Kraft, M.L., Elbedour, K., Yairi, Y., Musy, M., Skvorak, A.B., Van Camp, G., Srikumari Srisailapathy, C.R., Lovett, M., Morton, C.C., Sheffield, V.C., Smith, R.J.H., 1997. Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21. Genome Res. 7, 879-886.
-
(1997)
Genome Res.
, vol.7
, pp. 879-886
-
-
Greinwald J.H., Jr.1
Scott, D.A.2
Marietta, J.R.3
Carmi, R.4
Manaligod, J.5
Ramesh, A.6
Zbar, R.I.S.7
Kraft, M.L.8
Elbedour, K.9
Yairi, Y.10
Musy, M.11
Skvorak, A.B.12
Van Camp, G.13
Srikumari Srisailapathy, C.R.14
Lovett, M.15
Morton, C.C.16
Sheffield, V.C.17
Smith, R.J.H.18
-
4
-
-
0028837681
-
A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus
-
Jain, P.K., Fukushima, K., Deshmukh, D., Ramesh, A., Thomas, E., Lalwani, A.K., Kumar, S., Ploplis, B., Skarka, H., Srisailapathy, C.R.S., Wayne, S., Zbar, R.I.S., Verma, I.C., Smith, R.J.H., Wilcox, E.R., 1995. A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus. Hum. Mol. Genet. 4, 2391-2394.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2391-2394
-
-
Jain, P.K.1
Fukushima, K.2
Deshmukh, D.3
Ramesh, A.4
Thomas, E.5
Lalwani, A.K.6
Kumar, S.7
Ploplis, B.8
Skarka, H.9
Srisailapathy, C.R.S.10
Wayne, S.11
Zbar, R.I.S.12
Verma, I.C.13
Smith, R.J.H.14
Wilcox, E.R.15
-
5
-
-
0029159390
-
The deafness locus (dn) maps to mouse Chromosome 19
-
Keats, B.J.B., Nouri, N., Huang, J.-M., Webster, D.B., Berlin, C.I., 1995. The deafness locus (dn) maps to mouse Chromosome 19. Mamm. Genome 6, 8-10.
-
(1995)
Mamm. Genome
, vol.6
, pp. 8-10
-
-
Keats, B.J.B.1
Nouri, N.2
Huang, J.-M.3
Webster, D.B.4
Berlin, C.I.5
-
6
-
-
0344700299
-
-
Kelsell et al., 1997
-
Kelsell et al., 1997
-
-
-
-
7
-
-
0023665902
-
An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs
-
Kozak, M., 1987. An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15, 8125-8148.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 8125-8148
-
-
Kozak, M.1
-
8
-
-
0030960855
-
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
-
Liu, X.-Z., Walsh, J., Mburu, P., Kendrick-Jones, J., Cope, M.J.T.V., Steel, K.P., Brown, S.D.M., 1997. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nat. Genet. 16, 188-190.
-
(1997)
Nat. Genet.
, vol.16
, pp. 188-190
-
-
Liu, X.-Z.1
Walsh, J.2
Mburu, P.3
Kendrick-Jones, J.4
Cope, M.J.T.V.5
Steel, K.P.6
Brown, S.D.M.7
-
9
-
-
0026410464
-
Genetic epidemiology of hearing impairment
-
Morton, N.E., 1991. Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630, 16-31.
-
(1991)
Ann. NY Acad. Sci.
, vol.630
, pp. 16-31
-
-
Morton, N.E.1
-
10
-
-
0029807805
-
Genes responsible for human hereditary deafness: Symphony of a thousand
-
Petit, C., 1996. Genes responsible for human hereditary deafness: symphony of a thousand. Nat. Genet. 14, 385-391.
-
(1996)
Nat. Genet.
, vol.14
, pp. 385-391
-
-
Petit, C.1
-
11
-
-
0028169393
-
Isolation of novel and known genes from a human fetal cochlear cDNa library using subtractive hybridization and differential screening
-
Robertson, N.G., Khetarpal, U., Gutierrez-Espeleta, G.A., Bieber, F.R., Morton, C.C., 1994. Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening. Genomics 23, 42-50.
-
(1994)
Genomics
, vol.23
, pp. 42-50
-
-
Robertson, N.G.1
Khetarpal, U.2
Gutierrez-Espeleta, G.A.3
Bieber, F.R.4
Morton, C.C.5
-
12
-
-
0029811339
-
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds
-
Scott, D.A., Rivka, C., Elbedour, K., Yosefsberg, S., Stone, E.M., Sheffield, V.C., 1996. An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds. Am. J. Hum. Genet. 59, 385-391.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 385-391
-
-
Scott, D.A.1
Rivka, C.2
Elbedour, K.3
Yosefsberg, S.4
Stone, E.M.5
Sheffield, V.C.6
-
13
-
-
0028936930
-
Alterations in gene expression associated with changes in the state of endothelial differentiation
-
Shima, D.T., Saunders, K.B., Gougos, A., D'Amore, P.A., 1995. Alterations in gene expression associated with changes in the state of endothelial differentiation. Differentiation 58, 217-226.
-
(1995)
Differentiation
, vol.58
, pp. 217-226
-
-
Shima, D.T.1
Saunders, K.B.2
Gougos, A.3
D'Amore, P.A.4
-
15
-
-
26744466706
-
The mouse deafness locus (dn) is associated with an inversion on Chromosome 19
-
submitted
-
Viñas, A.M., Drury, S.S., De Angelis, M.M., Den, Z., Huang, J.M., Berlin, C.I., Hunt, J.D., Batzer, M.A., Deininger, P.L., Keats, B.J.B., 1998. The mouse deafness locus (dn) is associated with an inversion on Chromosome 19. Mamm. Genome, submitted.
-
(1998)
Mamm. Genome
-
-
Viñas, A.M.1
Drury, S.S.2
De Angelis, M.M.3
Den, Z.4
Huang, J.M.5
Berlin, C.I.6
Hunt, J.D.7
Batzer, M.A.8
Deininger, P.L.9
Keats, B.J.B.10
-
16
-
-
0030951102
-
The autosomal recessive isolated deafness, DFNB2, and the Usher IB syndrome are allelic defects of the myosin-VIIA gene
-
Weil, D., Kussel, P., Blanchard, S., Levy, G., Levi-Acobas, F., Drira, M., Ayadi, H., Petit, C., 1997. The autosomal recessive isolated deafness, DFNB2, and the Usher IB syndrome are allelic defects of the myosin-VIIA gene. Nat. Genet. 16, 191-193.
-
(1997)
Nat. Genet.
, vol.16
, pp. 191-193
-
-
Weil, D.1
Kussel, P.2
Blanchard, S.3
Levy, G.4
Levi-Acobas, F.5
Drira, M.6
Ayadi, H.7
Petit, C.8
-
17
-
-
0031923638
-
Passage to India: The search for genes causes autosomal recessive nonsyndromic hearing loss
-
Zbar, R.I.S., Ramesh, A., Srikumari Srisailapathy, C.R., Fukushima, K., Wayne, S., Smith, R.J.H., 1998. Passage to India: The search for genes causes autosomal recessive nonsyndromic hearing loss. Otolaryngol. Head Neck Surg. 118, 333-337.
-
(1998)
Otolaryngol. Head Neck Surg.
, vol.118
, pp. 333-337
-
-
Zbar, R.I.S.1
Ramesh, A.2
Srikumari Srisailapathy, C.R.3
Fukushima, K.4
Wayne, S.5
Smith, R.J.H.6
|