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American Journal of Medical Genetics|August 15, 2001
Frequency and ethnic distribution of the common DHCR7 mutation in Smith-Lemli-Opitz syndromeM J Nowaczyk, L M Nakamura, B Eng, et al.
Blood|October 1, 1993
X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phoxC D Porter, M H Parkar, R J Levinsky, et al.
The Journal of Infectious Diseases|July 1, 1988
Prominence of the herpes simplex virus latency-associated transcript in trigeminal ganglia from seropositive humansJ G Stevens, L Haarr, D D Porter, et al.
Analytical Chemistry|November 1, 2003
Femtomolar detection of prostate-specific antigen: an immunoassay based on surface-enhanced Raman scattering and immunogold labelsDesiree S Grubisha, Robert J Lipert, Hye-Young Park, et al.
Physiological Genomics|May 13, 2004
Conserved and muscle-group-specific gene expression patterns shape postnatal development of the novel extraocular muscle phenotypeGeorgiana Cheng, Anita P Merriam, Bendi Gong, et al.
Molecular Genetics and Metabolism|November 6, 2018
Necroptosis inhibition as a therapy for Niemann-Pick disease, type C1: Inhibition of RIP kinases and combination therapy with 2-hydroxypropyl-β-cyclodextrinA Cougnoux, S Clifford, A Salman, et al.
Computers and Biomedical Research, an International Journal|October 1, 1988
Self-service computerized bibliographic retrieval: a comparison of Colleague and PaperChase, programs that search the MEDLINE data baseD Porter, R S Wigton, M A Reidelbach, et al.
Pediatric Transplantation|November 28, 2023
Pediatric donor heart acceptance practices in the United States: What is really being considered?M A McCulloch, L P Alonzi, S C White, et al.
Accident; Analysis and Prevention|December 29, 2015
How the choice of safety performance function affects the identification of important crash prediction variablesKetong Wang, Jenna K Simandl, Michael D Porter, et al.
Developmental Medicine and Child Neurology|November 21, 2015
Cohort study of neurocognitive functioning and adaptive behaviour in children and adolescents with Niemann-Pick Disease type C1Audrey Thurm, Cristan Farmer, Nicole Yanjanin Farhat, et al.
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