Genotype and phenotype spectrum of NRAS germline variants.
European Journal Of Human Genetics : Ejhg
Altmüller, Franziska F; Lissewski, Christina C; Bertola, Debora D; Flex, Elisabetta E; Stark, Zornitza Z; Spranger, Stephanie S; Baynam, Gareth G; Buscarilli, Michelle M; Dyack, Sarah S; Gillis, Jane J; Yntema, Helger G HG; Pantaleoni, Francesca F; van Loon, Rosa LE RL; MacKay, Sara S; Mina, Kym K; Schanze, Ina I; Tan, Tiong Yang TY; Walsh, Maie M; White, Susan M SM; Niewisch, Marena R MR; García-Miñaúr, Sixto S; Plaza, Diego D; Ahmadian, Mohammad Reza MR; Cavé, Hélène H; Tartaglia, Marco M; Zenker, Martin M
Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43.
The Journal Of Investigative Dermatology
García, Isaac E IE; Maripillán, Jaime J; Jara, Oscar O; Ceriani, Ricardo R; Palacios-Muñoz, Angelina A; Ramachandran, Jayalakshmi J; Olivero, Pablo P; Perez-Acle, Tomas T; González, Carlos C; Sáez, Juan C JC; Contreras, Jorge E JE; Martínez, Agustín D AD
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Giannoulatou, Eleni E; McVean, Gilean G; Taylor, Indira B IB; McGowan, Simon J SJ; Maher, Geoffrey J GJ; Iqbal, Zamin Z; Pfeifer, Susanne P SP; Turner, Isaac I; Burkitt Wright, Emma M M EM; Shorto, Jennifer J; Itani, Aysha A; Turner, Karen K; Gregory, Lorna L; Buck, David D; Rajpert-De Meyts, Ewa E; Looijenga, Leendert H J LH; Kerr, Bronwyn B; Wilkie, Andrew O M AO; Goriely, Anne A
Retrotransposition and mutation events yield Rap1 GTPases with differential signalling capacity.
Bmc Evolutionary Biology
Zemojtel, Tomasz T; Duchniewicz, Marlena M; Zhang, Zhongchun Z; Paluch, Taisa T; Luz, Hannes H; Penzkofer, Tobias T; Scheele, Jürgen S JS; Zwartkruis, Fried J T FJ