Lmx1a maintains proper neurogenic, sensory, and non-sensory domains in the mammalian inner ear

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Fiona E. Karet, Karin E. Finberg, Raoul D. Nelson et al. · Nature Genetics · 1999 · 681 citations

Renal Function, Molecular Physiology, Biochemistry +8

Essential role of <i>BETA2/NeuroD1</i> in development of the vestibular and auditory systems

Min Liu, Fred A. Pereira, Steven D. Price et al. · Genes & Development · 2000 · 626 citations · Full text

Neurotology, Synaptic Signaling, Sensory Systems +25

Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome

Haixu Chen, Yi Lun, Dmitry A. Ovchinnikov et al. · Nature Genetics · 1998 · 570 citations

Developmental Biology, Genetic Disorder, Genetics +5

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

Sandra D. Dreyer, Guang Zhou, Antonio Baldini et al. · Nature Genetics · 1998 · 526 citations

Renal Dysplasia, Mendelian Disorder, Genetic Disorder +6

Development of the Mouse Inner Ear and Origin of Its Sensory Organs

Hakim Morsli, Daniel Choo, Allen F. Ryan et al. · Journal of Neuroscience · 1998 · 509 citations · Full text

Sensory Cell Development, Molecular Markers, Mouse Inner Ear +23