A O Vortmeyer|H J Colmant - JoVE Visualize

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Cancer Research|May 1, 1996

Barrett's esophagus: metaplastic cells with loss of heterozygosity at the APC gene locus are clonal precursors to invasive adenocarcinomaZ Zhuang, A O Vortmeyer, E J Mark, et al.

Human Pathology|March 7, 1998

Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevusW S Park, A O Vortmeyer, S Pack, et al.

Journal of the National Cancer Institute|August 6, 1997

Identical genetic changes in different histologic components of Wilms' tumorsZ Zhuang, M J Merino, A O Vortmeyer, et al.

The American Journal of Pathology|December 24, 1997

Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumorsE P Henske, L L Wessner, J Golden, 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.

Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 1999

VHL gene deletion and enhanced VEGF gene expression detected in the stromal cells of retinal angiomaC C Chan, A O Vortmeyer, E Y Chew, et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 9, 1999

Telomerase activity in microdissected human gliomasR J Weil, Y Y Wu, A O Vortmeyer, et al.

International Journal of Oncology|July 31, 1998

Mutations of the STK11 gene in sporadic gastric carcinomaW S Park, Y W Moon, Y M Yang, et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 25, 1999

Multiple endocrine neoplasia type 1: atypical presentation, clinical course, and genetic analysis of multiple tumorsA O Vortmeyer, I A Lubensky, M Skarulis, et al.

Cancer Research|December 5, 2000

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomasS C Huang, C A Koch, A O Vortmeyer, et al.

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Showing results (61-70 of 81) with videos related to

Sort By:

Pageof 9

Cancer Research|May 1, 1996

Barrett's esophagus: metaplastic cells with loss of heterozygosity at the APC gene locus are clonal precursors to invasive adenocarcinomaZ Zhuang, A O Vortmeyer, E J Mark, et al.

Human Pathology|March 7, 1998

Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevusW S Park, A O Vortmeyer, S Pack, et al.

Journal of the National Cancer Institute|August 6, 1997

Identical genetic changes in different histologic components of Wilms' tumorsZ Zhuang, M J Merino, A O Vortmeyer, et al.

The American Journal of Pathology|December 24, 1997

Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumorsE P Henske, L L Wessner, J Golden, 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.

Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 1999

VHL gene deletion and enhanced VEGF gene expression detected in the stromal cells of retinal angiomaC C Chan, A O Vortmeyer, E Y Chew, et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 9, 1999

Telomerase activity in microdissected human gliomasR J Weil, Y Y Wu, A O Vortmeyer, et al.

International Journal of Oncology|July 31, 1998

Mutations of the STK11 gene in sporadic gastric carcinomaW S Park, Y W Moon, Y M Yang, et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 25, 1999

Multiple endocrine neoplasia type 1: atypical presentation, clinical course, and genetic analysis of multiple tumorsA O Vortmeyer, I A Lubensky, M Skarulis, et al.

Cancer Research|December 5, 2000

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomasS C Huang, C A Koch, A O Vortmeyer, et al.

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