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Advances in Neurobiology|March 12, 2024
Fractal Electronics for Stimulating and Sensing Neural Networks: Enhanced Electrical, Optical, and Cell Interaction PropertiesS Moslehi, C Rowland, J H Smith, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 14, 2010
Dense deposit disease associated with monoclonal gammopathy of undetermined significanceSanjeev Sethi, William R Sukov, Yuzhou Zhang, et al.Cell|January 16, 2007
Manipulating the mouse genome to engineer precise functional syntenic replacements with human sequenceHelen A C Wallace, Fatima Marques-Kranc, Melville Richardson, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|August 24, 2004
Predicting outcome in ex-premature infants supported with extracorporeal membrane oxygenation for acute hypoxic respiratory failureK L Brown, G Walker, D J Grant, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 8, 2004
Metalloprotease-disintegrin ADAM8: expression analysis and targeted deletion in miceKristine Kelly, Gillian Hutchinson, Daniela Nebenius-Oosthuizen, et al.European Journal of Pediatrics|September 25, 2008
Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairmentKimia Kahrizi, Marzieh Mohseni, Carla Nishimura, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 22, 2016
C4 Glomerulopathy: A Disease Entity Associated With C4d DepositionSanjeev Sethi, Patrick S Quint, Conall M O'Seaghdha, et al.Prenatal Diagnosis|January 1, 1991
Cytogenetic studies of amniotic fluid taken before the 15th week of pregnancy for earlier prenatal diagnosis: a report of 114 consecutive casesM T Rebello, C T Gray, D E Rooney, et al.International Journal of Pediatric Otorhinolaryngology|December 4, 2003
GJB2 gene mutations causing familial hereditary deafness in TurkeyYildirim A Bayazit, Benjamin B Cable, Osman Cataloluk, et al.Human Mutation|September 15, 2004
GJB2: the spectrum of deafness-causing allele variants and their phenotypeHela Azaiez, G Parker Chamberlin, Stephanie M Fischer, et al.Pageof 71