E-LIB Suche - Ergebnisse für: Wilcox, Edward R.

1

Highly accurate long reads are crucial for realizing the po..:

Hotaling, Scott ; Wilcox, Edward R. ; Heckenhauer, Jacqueline..
BMC Genomics. 24 (2023) 1 - p. , 2023

2

Targeted Amplicon Sequencing (TAS): A Scalable Next-Gen App..:

Bybee, Seth M. ; Bracken-Grissom, Heather ; Haynes, Benjamin D....
Genome Biology and Evolution. 3 (2011) - p. 1312-1323 , 2011

Link: https://doi.org/10.1093/..

3

Mutation spectrum ofMYO7Aand evaluation of a novel nonsyndr..:

Riazuddin, Saima ; Nazli, Sabiha ; Ahmed, Zubair M....
Human Mutation. 29 (2008) 4 - p. 502-511 , 2008

Link: https://doi.org/10.1002/..

4

The Tip-Link Antigen, a Protein Associated with the Transdu..:

Ahmed, Zubair M. ; Goodyear, Richard ; Riazuddin, Saima...
The Journal of Neuroscience. 26 (2006) 26 - p. 7022-7034 , 2006

Link: https://doi.org/10.1523/..

5

DFNB48, a new nonsyndromic recessive deafness locus, maps t..:

Ahmad, Jamil ; Khan, Shaheen N. ; Khan, Shahid Y....
Human Genetics. 116 (2005) 5 - p. 407-412 , 2005

Link: https://doi.org/10.1007/..

6

Characterization of a new full length TMPRSS3 isoform and i..:

Ahmed, Zubair M ; Cindy Li, Xiaoyan ; Powell, Shontell D...
BMC Medical Genetics. 5 (2004) 1 - p. , 2004

Link: https://doi.org/10.1186/..

7

A new locus for nonsyndromic deafness DFNB49 maps to chromo..:

Ramzan, Khushnooda ; Shaikh, Rehan S. ; Ahmad, Jamil...
Human Genetics. 116 (2004) 1-2 - p. 17-22 , 2004

Link: https://doi.org/10.1007/..

8

Nonsyndromic recessive deafness DFNB18 and Usher syndrome t..:

Ahmed, Zubair M. ; Smith, Tenesha N. ; Riazuddin, Saima...
Human Genetics. 110 (2002) 6 - p. 527-531 , 2002

Link: https://doi.org/10.1007/..

9

Beethoven, a mouse model for dominant, progressive hearing ..:

Vreugde, Sarah ; Erven, Alexandra ; Kros, Corné J....
Nature Genetics. 30 (2002) 3 - p. 257-258 , 2002

Link: https://doi.org/10.1038/..

10

Dominant and recessive deafness caused by mutations of a no..:

Kurima, Kiyoto ; Peters, Linda M. ; Yang, Yandan...
Nature Genetics. 30 (2002) 3 - p. 277-284 , 2002

Link: https://doi.org/10.1038/..

11

Mutations in the Gene Encoding Tight Junction Claudin-14 Ca..:

Wilcox, Edward R ; Burton, Quianna L ; Naz, Sadaf...
Cell. 104 (2001) 1 - p. 165-172 , 2001

Link: https://doi.org/10.1016/..

12

Dominant modifier DFNM1 suppresses recessive deafness DFNB2:

Riazuddin, Saima ; Castelein, Caley M. ; Ahmed, Zubair M....
Nature Genetics. 26 (2000) 4 - p. 431-434 , 2000

Link: https://doi.org/10.1038/..

13

A mutation in PDS causes non-syndromic recessive deafness:

Li, Xiaoyan C. ; Everett, Lorraine A. ; Lalwani, Anil K....
Nature Genetics. 18 (1998) 3 - p. 215-217 , 1998

Link: https://doi.org/10.1038/..

14

Association of Unconventional Myosin MYO15 Mutations with H..:

Wang, Aihui ; Liang, Yong ; Fridell, Robert A....
Science. 280 (1998) 5368 - p. 1447-1451 , 1998

Link: https://www.jstor.org/st..

15

A Gene for Recessive Nonsyndromic Sensorineural Deafness (D..:

Jain, Pawan K. ; Lalwani, Anil K. ; Li, Xiaoyan C....
Genomics. 50 (1998) 2 - p. 290-292 , 1998

Link: https://doi.org/10.1006/..