The Relationship between Annual Airborne Pollen Levels and Occurrence of All Cancers, and Lung, Stomach, Colorectal, Pancreatic and Breast Cancers: A Retrospective Study from the National Registry Database of Cancer Incidence in Japan, 1975-2015
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The Relationship between Annual Airborne Pollen Levels and Occurrence of All Cancers, and Lung, Stomach, Colorectal, Pancreatic and Breast Cancers: A Retrospective Study from the National Registry Database of Cancer Incidence in Japan, 1975-2015
The emphasis of risk factors including smoking, overdrinking and infection by human papillomavirus and hepatitis B and C viruses have been recommended for the prevention of cancer; However, the identification of other environmental risk factors have not been enough. In addition to a 2003 report that Kawasaki disease can be triggered by exposure to pollen, 40 disease-specific hardware that Japan recently reported as “pollen disease,” also potentially triggered by pollen exposure.
Various human organs are affected by exposure to pollen, which leads to systemic vasculitis; autoimmune connective tissue disease, inflammatory bowel disease and bone and hard neuromuscular disease, show the general effects of exposure to pollen at fundamentally important metabolic functions. In this context, cancer and malignant tumors may be another group of intractable diseases triggered by exposure to pollen epigenetic. Thus, this study compared the number of newly registered patients with 24 types of cancer and pollen levels in the air were measured from 1975 to 2015. We are looking for statistical correlations with Bonferroni correction between the annual number of new patients registered for all cancers or for each lung -paru, stomach, colorectal, pancreatic and breast cancer in a patient-registry “x”, and the level of pollen in the air is measured yearly in the same year with “x”, or 1-7 years before the “x”.
The number of new patients registered for lung and pancreatic cancer in a patient-registry “x” was highly correlated with the level of pollen in the air is measured two years before the “x”. It’s breast cancer correlated with pollen levels were measured 2 and 5 years before the “x”. To our knowledge, this is the first rapid communication of the relationship between pollen levels and the incidence of cancer.
The Relationship between Annual Airborne Pollen Levels and Occurrence of All Cancers, and Lung, Stomach, Colorectal, Pancreatic and Breast Cancers: A Retrospective Study from the National Registry Database of Cancer Incidence in Japan, 1975-2015
psychological concerns of Indian women with breast cancer in different national contexts: a systematic review and mixed-methods of synthesis.
Breast cancer is the most common cancer among women of Indian origin. However, little is known about the psychological impact of the disease and treatment among this population. To enhance understanding of psychological symptoms among Indian women with breast cancer. This is a systematic review of the literature and critical interpretive synthesis. Medical Subject Headings (MeSH) terms and keywords for breast cancer, psychological symptoms and treatments that are used to search the database from the beginning till May 7, 2019. reference lists of articles including checked.
Search results filtered with inclusion criteria, data is retrieved, and the quality was assessed by two independent investigators with recourse to third. Narrative (quantitative) and qualitative thematic synthesis is applied, followed by a critical interpretive synthesis. ProQuest, MEDLINE, EMBASE Ovid, EBSCO, Cumulative Index to Nursing and Allied Health Literature, and PsycINFO. 18 of 763 studies from India or Canada included (13 quantitative, qualitative 5). critical interpretive synthesis found that psychological concerns are similar to women ‘West’, but has been used by the general culture of Indian women in both countries.
Description: Recognizes an unidentified antigen in the cytoplasm of mature granulocytes. It shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. SPM250 Ab reacts with early precursor and mature forms of human myeloid cells. This mAb is useful for the detection of myeloid leukemias and granulocytic sarcomas. It can be used as a marker of granulocytes in normal tissues or inflammatory processes.
Description: Recognizes an unidentified antigen in the cytoplasm of mature granulocytes. It shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. SPM250 Ab reacts with early precursor and mature forms of human myeloid cells. This mAb is useful for the detection of myeloid leukemias and granulocytic sarcomas. It can be used as a marker of granulocytes in normal tissues or inflammatory processes.
Description: Recognizes an unidentified antigen in the cytoplasm of mature granulocytes. It shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. SPM250 Ab reacts with early precursor and mature forms of human myeloid cells. This mAb is useful for the detection of myeloid leukemias and granulocytic sarcomas. It can be used as a marker of granulocytes in normal tissues or inflammatory processes.
Description: Recognizes an unidentified antigen in the cytoplasm of mature granulocytes. It shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. SPM250 Ab reacts with early precursor and mature forms of human myeloid cells. This mAb is useful for the detection of myeloid leukemias and granulocytic sarcomas. It can be used as a marker of granulocytes in normal tissues or inflammatory processes.
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Chemotactic Protein 2 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Chemotactic Protein 2 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Chemotactic Protein 2 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Colony Stimulating Factor in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Colony Stimulating Factor ELISA kit
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Colony Stimulating Factor in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Colony Stimulating Factor ELISA kit
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Colony Stimulating Factor in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Colony Stimulating Factor ELISA kit
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2)CLIA Kit
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2)CLIA Kit
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2)CLIA Kit
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2) CLIA Kit
Description: Double-antibody Sandwich chemiluminescent immunoassay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2)Serum, plasma and other biological fluids
Rat Granulocyte Chemotactic Protein 2 (GCP2) CLIA Kit
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2) ELISA Kit
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2) ELISA Kit
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2) ELISA Kit
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in serum, plasma and other biological fluids.
Rat Granulocyte Chemotactic Protein 2 (GCP2) ELISA Kit
Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Rat Granulocyte Chemotactic Protein 2 (GCP2) in samples from Serum, plasma and other biological fluids. with no significant corss-reactivity with analogues from other species.
Rat Granulocyte Chemotactic Protein 2 (GCP2) ELISA Kit
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Specific Antinuclear Antibody in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Specific Antinuclear Antibody ELISA kit
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Specific Antinuclear Antibody in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Specific Antinuclear Antibody ELISA kit
Description: A sandwich ELISA for quantitative measurement of Rat Granulocyte Specific Antinuclear Antibody in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Specific Antinuclear Antibody ELISA Kit
Description: This antibody recognizes an unidentified antigen in the cytoplasm of mature granulocytes and can be used as a granulocyte marker in normal tissues or inflammatory processes. The granulocyte marker antibody shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. Clone BM-2 mAb reacts with early precursor and mature forms of human myeloid cells. It is useful for the detection of myeloid leukemias and granulocytic sarcomas.
Description: This antibody recognizes an unidentified antigen in the cytoplasm of mature granulocytes and can be used as a granulocyte marker in normal tissues or inflammatory processes. The granulocyte marker antibody shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. Clone BM-2 mAb reacts with early precursor and mature forms of human myeloid cells. It is useful for the detection of myeloid leukemias and granulocytic sarcomas.
Description: This antibody recognizes an unidentified antigen in the cytoplasm of mature granulocytes and can be used as a granulocyte marker in normal tissues or inflammatory processes. The granulocyte marker antibody shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. Clone BM-2 mAb reacts with early precursor and mature forms of human myeloid cells. It is useful for the detection of myeloid leukemias and granulocytic sarcomas.
Description: This antibody recognizes an unidentified antigen in the cytoplasm of mature granulocytes and can be used as a granulocyte marker in normal tissues or inflammatory processes. The granulocyte marker antibody shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. Clone BM-2 mAb reacts with early precursor and mature forms of human myeloid cells. It is useful for the detection of myeloid leukemias and granulocytic sarcomas.
Granulocyte-Colony Stimulating Factor Rat Recombinant
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat GCP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat GCP2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat GCP2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat GCP2 in the samples is then determined by comparing the OD of the samples to the standard curve.
Rat GCP2(Granulocyte Chemotactic Protein 2) ELISA Kit
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat GCP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat GCP2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat GCP2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat GCP2 in the samples is then determined by comparing the OD of the samples to the standard curve.
Rat GCP2 (Granulocyte Chemotactic Protein 2) ELISA Kit
Description: A competitive ELISA for quantitative measurement of Rat Granulocyte colony-stimulating factor(CSF3) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte colony-stimulating factor(CSF3) ELISA kit
Description: A competitive ELISA for quantitative measurement of Rat Granulocyte colony-stimulating factor(CSF3) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte colony-stimulating factor(CSF3) ELISA kit
Description: A competitive ELISA for quantitative measurement of Rat Granulocyte colony-stimulating factor(CSF3) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte colony-stimulating factor (CSF3) ELISA Kit
Description: A competitive ELISA for quantitative measurement of Rat Granulocyte Colony Stimulating Factor Receptor in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Colony Stimulating Factor Receptor ELISA kit
Description: A competitive ELISA for quantitative measurement of Rat Granulocyte Colony Stimulating Factor Receptor in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Colony Stimulating Factor Receptor ELISA kit
Description: A competitive ELISA for quantitative measurement of Rat Granulocyte Colony Stimulating Factor Receptor in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Rat Granulocyte Colony Stimulating Factor Receptor ELISA kit
family structure, religion and society appears to protect against and cause distress in relation to the core role is expected to become a wife and mother and male dominance in decision making. Stigma was amplified by poor knowledge about the nature of cancer. Indian women migrants has additional problems because of language barriers. Indian women with breast cancer living in India and Canada psychological morbidity experience that greatly affects their role in the family and society at large.
