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Oncogene|October 14, 2000
Identification and characterization of JunD missense mutants that lack menin bindingJ I Knapp, C Heppner, A B Hickman, et al.
Oncogene|November 11, 1999
Stable overexpression of MEN1 suppresses tumorigenicity of RASY S Kim, A L Burns, P K Goldsmith, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2000
Genotype/phenotype correlation of multiple endocrine neoplasia type 1 gene mutations in sporadic gastrinomasS U Goebel, C Heppner, A L Burns, et al.
AJR. American Journal of Roentgenology|April 1, 1984
Detection of mediastinal parathyroid glands by nonselective digital arteriographyA G Krudy, J L Doppman, D L Miller, et al.
The American Journal of Pathology|September 11, 2001
Multiple leiomyomas of the esophagus, lung, and uterus in multiple endocrine neoplasia type 1J L McKeeby, X Li, Z Zhuang, et al.
The New England Journal of Medicine|May 15, 1986
Parathyroid mitogenic activity in plasma from patients with familial multiple endocrine neoplasia type 1M L Brandi, G D Aurbach, L A Fitzpatrick, et al.
Radiology|December 1, 1987
Angiographic ablation of parathyroid adenomas: lessons from a 10-year experienceD L Miller, J L Doppman, R Chang, et al.
Genetics and Molecular Research : GMR|June 15, 2017
Genetic diversity of Desmanthus sp accessions using ISSR markers and morphological traitsJ C Costa, G G M Fracetto, F J C Fracetto, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1990
Circulating fibroblast growth factor-like substance in familial multiple endocrine neoplasia type 1M B Zimering, M L Brandi, D A deGrange, et al.
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