Fex J - Search Results

1

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Lalwani AK, Brister JR, Fex J, Grundfast KM, Pikus AT, Ploplis B, San Agustin T, Skarka H, Wilcox ER. Lalwani AK, et al. Among authors: fex j. Am J Hum Genet. 1994 Oct;55(4):685-94. Am J Hum Genet. 1994. PMID: 7942846 Free PMC article.

2

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.

Wilcox ER, Rivolta MN, Ploplis B, Potterf SB, Fex J. Wilcox ER, et al. Among authors: fex j. Hum Mol Genet. 1992 Jun;1(3):215. doi: 10.1093/hmg/1.3.215-a. Hum Mol Genet. 1992. PMID: 1303187 No abstract available.

3

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families.

Lalwani AK, Brister JR, Fex J, Grundfast KM, Ploplis B, San Agustin TB, Wilcox ER. Lalwani AK, et al. Among authors: fex j. Am J Hum Genet. 1995 Jan;56(1):75-83. Am J Hum Genet. 1995. PMID: 7825605 Free PMC article.

4

Construction of a cDNA library from microdissected guinea pig crista ampullaris.

Wilcox ER, Fex J. Wilcox ER, et al. Among authors: fex j. Hear Res. 1994 Feb;73(1):65-6. doi: 10.1016/0378-5955(94)90283-6. Hear Res. 1994. PMID: 8157507

5

Construction of a cDNA library from microdissected guinea pig organ of Corti.

Wilcox ER, Fex J. Wilcox ER, et al. Among authors: fex j. Hear Res. 1992 Sep;62(1):124-6. doi: 10.1016/0378-5955(92)90208-5. Hear Res. 1992. PMID: 1358871

6

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Farrer LA, Grundfast KM, Amos J, Arnos KS, Asher JH Jr, Beighton P, Diehl SR, Fex J, Foy C, Friedman TB, et al. Farrer LA, et al. Among authors: fex j. Am J Hum Genet. 1992 May;50(5):902-13. Am J Hum Genet. 1992. PMID: 1349198 Free PMC article.

7

Selective amplification and partial sequencing of cDNAs encoding G protein alpha subunits from cochlear tissues.

Tachibana M, Wilcox E, Yokotani N, Schneider M, Fex J. Tachibana M, et al. Among authors: fex j. Hear Res. 1992 Sep;62(1):82-8. doi: 10.1016/0378-5955(92)90204-z. Hear Res. 1992. PMID: 1429253

8

G protein Gi2 alpha in the cochlea: cloning and selective occurrence in receptor cells.

Tachibana M, Asano T, Wilcox E, Yokotani N, Rivolta MN, Fex J. Tachibana M, et al. Among authors: fex j. Brain Res Mol Brain Res. 1994 Feb;21(3-4):355-8. doi: 10.1016/0169-328x(94)90267-4. Brain Res Mol Brain Res. 1994. PMID: 8170357

9

Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation.

Tachibana M, Hara Y, Vyas D, Hodgkinson C, Fex J, Grundfast K, Arnheiter H. Tachibana M, et al. Among authors: fex j. Mol Cell Neurosci. 1992 Oct;3(5):433-45. doi: 10.1016/1044-7431(92)90055-7. Mol Cell Neurosci. 1992. PMID: 19912887

10

Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.

Tachibana M, Perez-Jurado LA, Nakayama A, Hodgkinson CA, Li X, Schneider M, Miki T, Fex J, Francke U, Arnheiter H. Tachibana M, et al. Among authors: fex j. Hum Mol Genet. 1994 Apr;3(4):553-7. doi: 10.1093/hmg/3.4.553. Hum Mol Genet. 1994. PMID: 8069297

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