isis 5 software (MetaSystems inc)
90
Structured Review
MetaSystems inc
isis 5 software
Isis 5 Software, supplied by MetaSystems inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/isis+5+software/isis+5+software/pmc11668817-75-0-3
Average 90 stars, based on 1 article reviews
Isis 5 Software, supplied by MetaSystems inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/isis+5+software/isis+5+software/pmc11668817-75-0-3
Average 90 stars, based on 1 article reviews
isis 5 software - by Bioz Stars,
2026-09
90/100 stars
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Software:Article Title: Generation and characterization of two induced pluripotent stem cell lines (ICGi052-A and ICGi052-B) from a patient with frontotemporal dementia with parkinsonism-17 associated with the pathological variant c.2013T>G in the MAPT gene Article Snippet: Chromosome analysis was performed under an Axioplan 2 microscope (Zeiss) equipped with a CV-M 300 CCD camera (JAI Corp.) at the Common Use Center of Microscopy of Biological Objects (https://ckp.icgen.ru/ckpmabo) at the Institute of Cytology and Genetics SB RAS. .. Article Title: Novel MAP4::RAF1 Fusion in a Primary Bone Sarcoma: Expanding the spectrum of RAF1 Fusion Sarcoma. Article Snippet: Soft tissue tumors with RAF1 fusion had been emerging as a group of tumors with peculiar histology and immunoprofile.. While a case series and rare case reports of RAF1 translocated sarcoma had been reported, to our knowledge a primary bone tumor with RAF1 translocation and fusion partner withMAP4 had not been described in the literature.. The patient was a 60-year-old lady, with strong family history of breast cancer, who presented with pathological fracture of right humerus. Article Title: A group of sclerosing epithelioid fibrosarcomas with low-level amplified EWSR1-CREB3L1 fusion gene in children. Article Snippet: Sclerosing epithelioid fibrosarcoma (SEF), typically arising in middle-aged and older adults, is a rare malignant fibroblastic neoplasm characterized by epithelioid fibroblasts embedded in sclerotic hyalinized stroma.. This tumor frequently harbors translocation between EWSR1 and CREB3 subfamily members.. Here, we describe four cases of SEF with unique genetic characteristics in children. Article Title: DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays Article Snippet: .. Image z-stacks were captured using a Zeiss Axioplan 2 motorized microscope controlled by Article Title: RREB1::MRTFB Fusion Positive Extra-glossal Mesenchymal Neoplasms: A Series of Five Cases Expanding Their Anatomic Distribution And Highlighting Significant Morphological and Phenotypic Diversity Article Snippet: .. Two hundred successive nuclei were examined using a Zeiss fluorescence microscope (Zeiss Axioplan, Oberkochen, Germany), controlled by Article Title: Expanding the spectrum of mesenchymal neoplasms with NR1D1-rearrangement. Article Snippet: Department of Anatomic and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA Department of Orthopedics and Traumatology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China Department of Pathology and Laboratory Medicine, Mount Sinai Health System, Toronto, Ontario, Canada Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada Department of Surgery, Mount Sinai Health System, Toronto, Ontario, Canada Division of Orthopaedics, Department of Surgery, University of Toronto, Toronto, Ontario, Canada Article Title: Clinical relevance of BCOR internal tandem duplication and TP53 aberration in clear cell sarcoma of the kidney. Article Snippet: .. A total of 200 intact nuclei were examined using a Zeiss fluorescence microscope (Scope.A1, Zeiss, Oberkochen, Germany) and Article Title: Detection of ER Stress in iPSC-Derived Neurons Carrying the p.N370S Mutation in the GBA1 Gene. Article Snippet: Karyotype analysis was performed using an Axioplan 2 microscope (Zeiss, Oberkochen, Germany) equipped with a CV-M300 CCD camera (JAI Corp., Yokohama, Japan) at the Core Facility of Microscopic Analysis of Biological Objects at the Institute of Cytology and Genetics, SB RAS. .. Fluorescence:Article Title: Novel MAP4::RAF1 Fusion in a Primary Bone Sarcoma: Expanding the spectrum of RAF1 Fusion Sarcoma. Article Snippet: Soft tissue tumors with RAF1 fusion had been emerging as a group of tumors with peculiar histology and immunoprofile.. While a case series and rare case reports of RAF1 translocated sarcoma had been reported, to our knowledge a primary bone tumor with RAF1 translocation and fusion partner withMAP4 had not been described in the literature.. The patient was a 60-year-old lady, with strong family history of breast cancer, who presented with pathological fracture of right humerus. Article Title: A group of sclerosing epithelioid fibrosarcomas with low-level amplified EWSR1-CREB3L1 fusion gene in children. Article Snippet: Sclerosing epithelioid fibrosarcoma (SEF), typically arising in middle-aged and older adults, is a rare malignant fibroblastic neoplasm characterized by epithelioid fibroblasts embedded in sclerotic hyalinized stroma.. This tumor frequently harbors translocation between EWSR1 and CREB3 subfamily members.. Here, we describe four cases of SEF with unique genetic characteristics in children. Article Title: RREB1::MRTFB Fusion Positive Extra-glossal Mesenchymal Neoplasms: A Series of Five Cases Expanding Their Anatomic Distribution And Highlighting Significant Morphological and Phenotypic Diversity Article Snippet: .. Two hundred successive nuclei were examined using a Zeiss fluorescence microscope (Zeiss Axioplan, Oberkochen, Germany), controlled by Article Title: Expanding the spectrum of mesenchymal neoplasms with NR1D1-rearrangement. Article Snippet: Department of Anatomic and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA Department of Orthopedics and Traumatology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China Department of Pathology and Laboratory Medicine, Mount Sinai Health System, Toronto, Ontario, Canada Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada Department of Surgery, Mount Sinai Health System, Toronto, Ontario, Canada Division of Orthopaedics, Department of Surgery, University of Toronto, Toronto, Ontario, Canada Article Title: Clinical relevance of BCOR internal tandem duplication and TP53 aberration in clear cell sarcoma of the kidney. Article Snippet: .. A total of 200 intact nuclei were examined using a Zeiss fluorescence microscope (Scope.A1, Zeiss, Oberkochen, Germany) and Microscopy:Article Title: Novel MAP4::RAF1 Fusion in a Primary Bone Sarcoma: Expanding the spectrum of RAF1 Fusion Sarcoma. Article Snippet: Soft tissue tumors with RAF1 fusion had been emerging as a group of tumors with peculiar histology and immunoprofile.. While a case series and rare case reports of RAF1 translocated sarcoma had been reported, to our knowledge a primary bone tumor with RAF1 translocation and fusion partner withMAP4 had not been described in the literature.. The patient was a 60-year-old lady, with strong family history of breast cancer, who presented with pathological fracture of right humerus. Article Title: A group of sclerosing epithelioid fibrosarcomas with low-level amplified EWSR1-CREB3L1 fusion gene in children. Article Snippet: Sclerosing epithelioid fibrosarcoma (SEF), typically arising in middle-aged and older adults, is a rare malignant fibroblastic neoplasm characterized by epithelioid fibroblasts embedded in sclerotic hyalinized stroma.. This tumor frequently harbors translocation between EWSR1 and CREB3 subfamily members.. Here, we describe four cases of SEF with unique genetic characteristics in children. Article Title: DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays Article Snippet: .. Image z-stacks were captured using a Zeiss Axioplan 2 motorized microscope controlled by Article Title: RREB1::MRTFB Fusion Positive Extra-glossal Mesenchymal Neoplasms: A Series of Five Cases Expanding Their Anatomic Distribution And Highlighting Significant Morphological and Phenotypic Diversity Article Snippet: .. Two hundred successive nuclei were examined using a Zeiss fluorescence microscope (Zeiss Axioplan, Oberkochen, Germany), controlled by Article Title: Expanding the spectrum of mesenchymal neoplasms with NR1D1-rearrangement. Article Snippet: Department of Anatomic and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA Department of Orthopedics and Traumatology, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China Department of Pathology and Laboratory Medicine, Mount Sinai Health System, Toronto, Ontario, Canada Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada Department of Surgery, Mount Sinai Health System, Toronto, Ontario, Canada Division of Orthopaedics, Department of Surgery, University of Toronto, Toronto, Ontario, Canada Article Title: Clinical relevance of BCOR internal tandem duplication and TP53 aberration in clear cell sarcoma of the kidney. Article Snippet: .. A total of 200 intact nuclei were examined using a Zeiss fluorescence microscope (Scope.A1, Zeiss, Oberkochen, Germany) and Incubation:Article Title: A group of sclerosing epithelioid fibrosarcomas with low-level amplified EWSR1-CREB3L1 fusion gene in children. Article Snippet: Sclerosing epithelioid fibrosarcoma (SEF), typically arising in middle-aged and older adults, is a rare malignant fibroblastic neoplasm characterized by epithelioid fibroblasts embedded in sclerotic hyalinized stroma.. This tumor frequently harbors translocation between EWSR1 and CREB3 subfamily members.. Here, we describe four cases of SEF with unique genetic characteristics in children. Staining:Article Title: A group of sclerosing epithelioid fibrosarcomas with low-level amplified EWSR1-CREB3L1 fusion gene in children. Article Snippet: Sclerosing epithelioid fibrosarcoma (SEF), typically arising in middle-aged and older adults, is a rare malignant fibroblastic neoplasm characterized by epithelioid fibroblasts embedded in sclerotic hyalinized stroma.. This tumor frequently harbors translocation between EWSR1 and CREB3 subfamily members.. Here, we describe four cases of SEF with unique genetic characteristics in children. |