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The American Journal of Pathology
|
September 1, 1993
Pancreatic acinar cell carcinoma. An analysis of cell lineage markers, p53 expression, and Ki-ras mutation
A Hoorens, N R Lemoine, E McLellan, et al.
Analytical and Quantitative Cytology and Histology
|
May 1, 1987
Morphometry and immunocytochemistry
M Oberholzer, R A Ettlin, G Klöppel, et al.
The Journal of Pathology
|
August 28, 2001
Deletion at 3p25.3-p23 is frequently encountered in endocrine pancreatic tumours and is associated with metastatic progression
A Barghorn, P Komminoth, D Bachmann, et al.
The American Journal of Pathology
|
November 7, 1999
Mixed medullary-follicular thyroid carcinoma. Molecular evidence for a dual origin of tumor components
M Volante, M Papotti, J Roth, et al.
Der Pathologe
|
January 1, 1991
[Definition and clinical significance of dysplasia in the digestive tract. Results of a meeting of the Society of Gastroenterologic Pathology of the German Society of Pathology 25 November 1989 in Kronberg]
F Borchard, K L Heilmann, P Hermanek, et al.
The American Journal of Pathology
|
December 14, 1999
Genetic differences in endocrine pancreatic tumor subtypes detected by comparative genomic hybridization
E J Speel, J Richter, H Moch, et al.
The American Journal of Pathology
|
November 14, 2000
Genomic alterations in well-differentiated gastrointestinal and bronchial neuroendocrine tumors (carcinoids): marked differences indicating diversity in molecular pathogenesis
J Zhao, R R de Krijger, D Meier, et al.
The New England Journal of Medicine
|
March 15, 1990
Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome
M Pipeleers-Marichal, G Somers, G Willems, et al.
The American Journal of Pathology
|
February 23, 1999
Mutations and allelic deletions of the MEN1 gene are associated with a subset of sporadic endocrine pancreatic and neuroendocrine tumors and not restricted to foregut neoplasms
B Görtz, J Roth, A Krähenmann, et al.
Schweizerische Medizinische Wochenschrift
|
August 6, 1996
[Detection of RET-proto-oncogene mutations in the diagnosis of Type 2 endocrine neoplasia (MEN 2)]
P Komminoth, S Muletta-Feurer, A Soltermann, et al.
Page
of 24
Search research articles
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Showing results (221-230 of 236) with videos related to
Sort By:
Page
of 24
The American Journal of Pathology
|
September 1, 1993
Pancreatic acinar cell carcinoma. An analysis of cell lineage markers, p53 expression, and Ki-ras mutation
A Hoorens, N R Lemoine, E McLellan, et al.
Analytical and Quantitative Cytology and Histology
|
May 1, 1987
Morphometry and immunocytochemistry
M Oberholzer, R A Ettlin, G Klöppel, et al.
The Journal of Pathology
|
August 28, 2001
Deletion at 3p25.3-p23 is frequently encountered in endocrine pancreatic tumours and is associated with metastatic progression
A Barghorn, P Komminoth, D Bachmann, et al.
The American Journal of Pathology
|
November 7, 1999
Mixed medullary-follicular thyroid carcinoma. Molecular evidence for a dual origin of tumor components
M Volante, M Papotti, J Roth, et al.
Der Pathologe
|
January 1, 1991
[Definition and clinical significance of dysplasia in the digestive tract. Results of a meeting of the Society of Gastroenterologic Pathology of the German Society of Pathology 25 November 1989 in Kronberg]
F Borchard, K L Heilmann, P Hermanek, et al.
The American Journal of Pathology
|
December 14, 1999
Genetic differences in endocrine pancreatic tumor subtypes detected by comparative genomic hybridization
E J Speel, J Richter, H Moch, et al.
The American Journal of Pathology
|
November 14, 2000
Genomic alterations in well-differentiated gastrointestinal and bronchial neuroendocrine tumors (carcinoids): marked differences indicating diversity in molecular pathogenesis
J Zhao, R R de Krijger, D Meier, et al.
The New England Journal of Medicine
|
March 15, 1990
Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome
M Pipeleers-Marichal, G Somers, G Willems, et al.
The American Journal of Pathology
|
February 23, 1999
Mutations and allelic deletions of the MEN1 gene are associated with a subset of sporadic endocrine pancreatic and neuroendocrine tumors and not restricted to foregut neoplasms
B Görtz, J Roth, A Krähenmann, et al.
Schweizerische Medizinische Wochenschrift
|
August 6, 1996
[Detection of RET-proto-oncogene mutations in the diagnosis of Type 2 endocrine neoplasia (MEN 2)]
P Komminoth, S Muletta-Feurer, A Soltermann, et al.
Page
of 24