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Surgery|December 1, 1995
Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinomaA Frilling, H Dralle, C Eng, et al.Nature|January 15, 1998
A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.American Journal of Physiology. Heart and Circulatory Physiology|June 19, 2001
Changes in collagenase and collagen gene expression after induction of aortocaval fistula in ratsS M Dolgilevich, F M Siri, S A Atlas, et al.Oncogene|November 16, 1995
Characterization of RET proto-oncogene 3' splicing variants and polyadenylation sites: a novel C-terminus for RETS M Myers, C Eng, B A Ponder, et al.Cancer Research|January 13, 2001
Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytomaO Gimm, M Armanios, H Dziema, et al.The Plant Cell|March 11, 2026
CESA7 and microtubules pattern complex secondary cell walls in explosive fruit of Cardamine hirsutaRyan C Eng, Aurélia Emonet, Ulla Neumann, et al.Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.International Journal of Cancer|April 3, 1999
Cancer risk in mutation carriers of DNA-mismatch-repair genesM Aarnio, R Sankila, E Pukkala, et al.The American Journal of Pathology|September 11, 2001
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathologyM Kiuru, V Launonen, M Hietala, et al.Cancer Research|December 15, 1993
Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndromeP Peltomäki, R A Lothe, L A Aaltonen, et al.Pageof 145