DavidBishopMD

PubMed

• 20 citations
  The Feasibility of a Health Care Application in the Treatment of Patients Undergoing Radical Cystectomy.
  Meredith Metcalf, Vassili Glazyrine, Katie Glavin, Alexandra Dahlgren, Carrie Michael, Misty D. Bechtel, David Bishop, Martin DeRuyter, Moben Mirza, John A. Taylor, Ha...> ;The Journal of Urology. 2019 May 1
• Molecular expression, characterization and mechanism of ALAS2 gain-of-function mutants.
  Tchaikovskii, V.,Desnick, R. J.,Bishop, D. F.> ;Mol. Med.. 2019 Jan 27
• Diagnosis of feline acute intermittent porphyria presenting with erythrodontia requires molecular analyses.
  Clavero S, Ahuja Y, Bishop DF, Kwait B, Haskins ME, Giger U, Desnick RJ> ;Vet. J.. 2013-12-01
• Loss-of-function ferrochelatase and gain-of-function erythroid-specific 5-aminolevulinate synthase mutations causing erythropoietic protoporphyria and x-linked protopo...
  Balwani M, Doheny D, Bishop DF, Nazarenko I, Yasuda M, Dailey HA, Anderson KE, Bissell DM, Bloomer J, Bonkovsky HL, Phillips JD, Liu L, Desnick RJ> ;Mol. Med.. 2013-04-30
• Molecular expression and characterization of erythroid-specific 5-aminolevulinate synthase gain-of-function mutations causing X-linked protoporphyria.
  Bishop DF, Tchaikovskii V, Nazarenko I, Desnick RJ> ;Mol. Med.. 2013-03-05
• A LC-MS/MS method for the specific, sensitive, and simultaneous quantification of 5-aminolevulinic acid and porphobilinogen.
  Zhang J, Yasuda M, Desnick RJ, Balwani M, Bishop D, Yu C> ;J. Chromatogr. B Analyt. Technol. Biomed. Life Sci.. 2011-08-15
• Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.
  Hasanoglu A, Balwani M, Kasapkara CS, Ezgü FS, Okur I, Tümer L, Cakmak A, Nazarenko I, Yu C, Clavero S, Bishop DF, Desnick RJ> ;J. Inherit. Metab. Dis.. 2011-02-01
• Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.
  Clavero S, Bishop DF, Haskins ME, Giger U, Kauppinen R, Desnick RJ> ;Hum. Mol. Genet.. 2010-02-15
• Congenital erythropoietic porphyria: a novel uroporphyrinogen III synthase branchpoint mutation reveals underlying wild-type alternatively spliced transcripts.
  Bishop DF, Schneider-Yin X, Clavero S, Yoo H, Minder EI, Desnick RJ> ;Blood. 2010-02-04
• Feline congenital erythropoietic porphyria: two homozygous UROS missense mutations cause the enzyme deficiency and porphyrin accumulation.
  Clavero S, Bishop DF, Giger U, Haskins ME, Desnick RJ> ;Mol. Med.. 2010-01-01
• Congenital erythropoietic porphyria: characterization of murine models of the severe common (C73R/C73R) and later-onset genotypes.
  Bishop, D. F.,Clavero, S.,Mohandas, N.,Desnick, R. J.> ;Mol. Med.. 2011 Mar 03
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