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European Journal of Endocrinology|October 17, 2018
Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencingRafael A Carvalho, Betsaida Urtremari, Alexander A L Jorge, et al.
Plos Computational Biology|August 15, 2015
Controlled Measurement and Comparative Analysis of Cellular Components in E. coli Reveals Broad Regulatory Changes in Response to Glucose StarvationJohn R Houser, Craig Barnhart, Daniel R Boutz, et al.
Cancer Discovery|July 11, 2012
CD36 repression activates a multicellular stromal program shared by high mammographic density and tumor tissuesRosa Anna DeFilippis, Hang Chang, Nancy Dumont, et al.
Scientific Reports|April 19, 2017
The E. coli molecular phenotype under different growth conditionsMehmet U Caglar, John R Houser, Craig S Barnhart, et al.
Cancer Research|March 15, 1997
Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) geneL V Debelenko, M R Emmert-Buck, P Manickam, et al.
Cancer Research|November 25, 2003
Parathyroid gland-specific deletion of the mouse Men1 gene results in parathyroid neoplasia and hypercalcemic hyperparathyroidismSteven K Libutti, Judy S Crabtree, Dominique Lorang, et al.
Surgery|December 5, 2009
Reoperation for parathyroid adenoma: a contemporary experienceAnathea C Powell, H Richard Alexander, Richard Chang, et al.
Surgery|December 14, 2001
Reoperation for hyperparathyroidism in multiple endocrine neoplasia type 1M H Kivlen, D L Bartlett, S K Libutti, et al.
Cancer Research|May 15, 1997
Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysisM R Emmert-Buck, I A Lubensky, Q Dong, et al.
Molecular Genetics and Metabolism|May 1, 1998
11q13 allelotype analysis in 27 northern American MEN1 kindreds identifies two distinct founder chromosomesM R Emmert-Buck, L V Debelenko, S Agarwal, et al.
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