The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

By Reed Danielle R.   Zhu Gu   Breslin Paul A.S.   Duke Fujiko F.   Henders Anjali K.   Campbell Megan J.   Montgomery Grant W.   Medland Sarah E.   Martin Nicholas G.   Wright Margaret J.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4278-4285

Oxford University Press

Access to resources Recommend Favorite

Non-Coding Loss-of-Function Variation in Human Genomes

By  

Human Heredity, Vol. 81, Iss. 2, 2017-01 ,pp. : 78-87

Karger

Access to resources Recommend Favorite

Maternal expression increases the rate of bicoid evolution by relaxing selective constraint

By Demuth Jeffery   Wade Michael  

Genetica, Vol. 129, Iss. 1, 2007-01 ,pp. : 37-43

Springer Publishing Company

Access to resources Recommend Favorite

PTHR1 mutations associated with Ollier disease result in receptor loss of function

By Couvineau Alain   Wouters Vinciane   Bertrand Guylne   Rouyer Christiane   Grard Bndicte   Boon Laurence M.   Grandchamp Bernard   Vikkula Miikka   Silve Caroline  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2766-2775

Oxford University Press

Access to resources Recommend Favorite

Mutations in the human SIX3 gene in holoprosencephaly are loss of function

By Domen Sabina   Roessler Erich   El-Jaick Kenia B.   Snir Mirit   Brown Jamie L.   Vlez Jorge I.   Bale Sherri   Lacbawan Felicitas   Muenke Maximilian   Feldman Benjamin  

Human Molecular Genetics, Vol. 17, Iss. 24, 2008-12 ,pp. : 3919-3928

Oxford University Press

Access to resources Recommend Favorite