المؤلفون: Jens Plaschke, Stefan Krüger, Birgit Jeske, Contact The Aacr

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://cancerres.aacrjournals.org/content/64/3/864.full.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.327.7879Test; http://cancerres.aacrjournals.org/content/64/3/864.full.pdfTest

الإتاحة: http://cancerres.aacrjournals.org/content/64/3/864.full.pdfTest

المؤلفون: Giancarlo Marra, Theissig F, Ingram Iaccarino, Jens Plaschke, Stefan Krüger, Steffen Pistorius, Hans Detlev Saeger, Friedmar Kreuz, Birgit Jeske, Hans K. Schackert

المساهمون: University of Zurich, Plaschke, J

المصدر: Cancer research (Chic. Ill.) 64 (2004): 864–870. doi:10.1158/0008-5472.CAN-03-2807
info:cnr-pdr/source/autori:Plaschke J.; Kruger S.; Jeske B.; Theissig F.; Kreuz F.R.; Pistorius S.; Saeger H.D.; Iaccarino I.; Marra G.; Schackert H.K./titolo:Loss of MSH3 protein expression is frequent in MLH1-deficient colorectal cancer and is associated with disease progression/doi:10.1158%2F0008-5472.CAN-03-2807/rivista:Cancer research (Chic. Ill.)/anno:2004/pagina_da:864/pagina_a:870/intervallo_pagine:864–870/volume:64

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Pathology, medicine.medical_specialty, Colorectal cancer, Loss of Heterozygosity, Biology, MLH1, Frameshift mutation, Loss of heterozygosity, medicine, Humans, 1306 Cancer Research, Frameshift Mutation, Alleles, Adaptor Proteins, Signal Transducing, Neoplasm Staging, 10061 Institute of Molecular Cancer Research, Nuclear Proteins, medicine.disease, Immunohistochemistry, digestive system diseases, Neoplasm Proteins, DNA-Binding Proteins, MSH6, Oncology, MSH3, MSH2, Tumor progression, Lymphatic Metastasis, MutS Homolog 3 Protein, Disease Progression, Cancer research, 570 Life sciences, biology, 2730 Oncology, Carrier Proteins, Colorectal Neoplasms, MutL Protein Homolog 1

وصف الملف: m864.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53baa30304a9b25b792e0507d723f8d2Test
https://doi.org/10.1158/0008-5472.can-03-2807Test

المؤلفون: Stefan, Krüger, Jens, Plaschke, Birgit, Jeske, Heike, Görgens, Steffen R, Pistorius, Andrea, Bier, Friedmar R, Kreuz, Franz, Theissig, Daniela E, Aust, Hans D, Saeger, Hans K, Schackert

المصدر: Human mutation. 21(4)

مصطلحات موضوعية: Male, Nuclear Proteins, Middle Aged, Colorectal Neoplasms, Hereditary Nonpolyposis, Neoplasm Proteins, DNA-Binding Proteins, MutS Homolog 2 Protein, Proto-Oncogene Proteins, Humans, Female, Carrier Proteins, MutL Protein Homolog 1, Germ-Line Mutation, Adaptor Proteins, Signal Transducing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::aeb9a2a26e86b969c6743d1112f9c7a7Test
https://pubmed.ncbi.nlm.nih.gov/12655562Test

المؤلفون: Stefan, Krüger, Jens, Plaschke, Steffen, Pistorius, Birgit, Jeske, Stephan, Haas, Heike, Krämer, Irene, Hinterseher, Andrea, Bier, Friedmar R, Kreuz, Franz, Theissig, Hans D, Saeger, Hans K, Schackert

المصدر: Human mutation. 19(1)

مصطلحات موضوعية: Adult, Male, DNA Mutational Analysis, Nuclear Proteins, DNA, Neoplasm, Middle Aged, Colorectal Neoplasms, Hereditary Nonpolyposis, Neoplasm Proteins, DNA-Binding Proteins, MutS Homolog 2 Protein, Proto-Oncogene Proteins, Humans, Female, Age of Onset, Carrier Proteins, MutL Protein Homolog 1, Omentum, Germ-Line Mutation, Peritoneal Neoplasms, Adaptor Proteins, Signal Transducing, Aged

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::4e39cd14a59af1ab4ad89a79fb7eb18dTest
https://pubmed.ncbi.nlm.nih.gov/11754112Test

المؤلفون: Jens Plaschke, Steffen Pistorius, Theissig F, Friedmar Kreuz, Heike Görgens, Andrea Bier, Stefan Krüger, Birgit Jeske, Hans K. Schackert, Daniela Aust, Hans Detlev Saeger

المصدر: Human Mutation. 21:445-446

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Mutation, Splice site mutation, Nonsense mutation, nutritional and metabolic diseases, Biology, medicine.disease_cause, MLH1, Molecular biology, digestive system diseases, Germline mutation, MSH2, medicine, PMS2, Missense mutation, neoplasms, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a98340e291f89f7ccbdedb47e40fc932Test
https://doi.org/10.1002/humu.9121Test

المؤلفون: Irene Hinterseher, Heike Krämer, Hans K. Schackert, Birgit Jeske, Stephan Haas, Jens Plaschke, Hans Detlev Saeger, Steffen Pistorius, Andrea Bier, Stefan Krüger, Theissig F, Friedmar Kreuz

المصدر: Human Mutation. 19:82-82

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Amsterdam criteria, Nonsense mutation, nutritional and metabolic diseases, Microsatellite instability, Biology, MLH1, medicine.disease, digestive system diseases, Stop codon, Germline mutation, MSH2, medicine, Missense mutation, neoplasms, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c40ff53cb8c46a15d7e1f9a9a3d3da60Test
https://doi.org/10.1002/humu.9004Test