Concepedia

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay, Inna A. Belyantseva, Mohamed Ali Mosrati, Rob W.J. Collin, Saima Riazuddin, Mounira Hmani‐Aifa, Hanka Venselaar, Mayya N Kawar,

Nature Genetics · 2008 · 87 citations · 24 references

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24

Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest

Dawn E. Ouelle, Frédérique Zindy, Richard A. Ashmun et al. · Cell · 1995 · 1.5K citations · Full text

, , +17

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

M. Charles Liberman, Jiangang Gao, David Z. Z. He et al. · Nature · 2002 · 936 citations

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Catechol- <i>O</i> -methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

Joseph A. Gogos, Maria A. Morgan, Victoria N. Luine et al. · Proceedings of the National Academy of Sciences · 1998 · 855 citations · Full text

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Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

Zubair M. Ahmed, Saima Riazuddin, Steven L. Bernstein et al. · The American Journal of Human Genetics · 2001 · 414 citations · Full text

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Suggestions for “safe” residue substitutions in site-directed mutagenesis

Domenico Bordo, Patrick Argos · Journal of Molecular Biology · 1991 · 384 citations

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