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antibodybased immunohistochemistry ihc data across normal tissues  (Human Protein Atlas)

 
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    Human Protein Atlas antibodybased immunohistochemistry ihc data across normal tissues
    Antibodybased Immunohistochemistry Ihc Data Across Normal Tissues, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+tissue+data/ihc+immunohistochemistry/pm42118406-88-15-3
    Average 86 stars, based on 1 article reviews
    antibodybased immunohistochemistry ihc data across normal tissues - by Bioz Stars, 2026-09
    86/100 stars

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    other:

    Article Title: A paradigm shift in cancer research based on integrative multi-omics approaches: glutaminase serves as a pioneering cuproptosis-related gene in pan-cancer
    Article Snippet: Normal tissue data were downloaded from the Human Protein Atlas (HPA) database (integration of proteomic data across various tissues and cell types) ( https://www.proteinatlas.org/ ) [ ], and the data from cancer cell lines were acquired from the Cancer Cell Line Encyclopedia (CCLE) database (Encompassing the most comprehensive gene data from human cancer cell lines) ( https://sites.broadinstitute.org/ccle/ ) [ ].

    Article Title: Effects of different kinds of essentiality on sequence evolution of human testis proteins
    Article Snippet: Proteins expressed in the seminiferous ducts of human testis under physiological conditions were extracted from “normal tissue” data of the Human Protein Atlas ( http://www.proteinatlas.org/ ) version 12.

    Article Title: A short C-terminal peptide in Gγ regulates Gβγ signaling efficacy
    Article Snippet: Data are extracted from the Normal tissue data available in The Human Protein Atlas database.

    Expressing:

    Article Title:
    Article Snippet: .. For RAB32 protein expression we downloaded normal tissue data from Human Protein Atlas https://www.proteinatlas.org/, accessed on 02/08/2023). ..

    Article Title: Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning
    Article Snippet: Human Protein Atlas data are publicly available at: https://www.proteinatlas.org/about/download (version 18.1, last accessed on 06/03/2019). .. We integrate two types of data from Human Protein Atlas: Normal tissue data (normal_tissue.tsv), which contain levels of expression for each gene in different tissues and cell types (categorical variable: ‘Not detected’, ‘Low’, ‘Medium’, ‘High’) and RNA gene data (rna_tissue.tsv), which contain TPM expression values for each gene by Sample (where ‘Sample’ in this case is similar with the ‘Tissue’ field from Normal tissue data). ..

    Article Title: Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum
    Article Snippet: .. Finally, we correlated the somatic instability indices with the expression of FGF14 in normal tissue data from the Human Protein Atlas (HPA v.23.0; proteinatlas.org accessed 27 March 2024). ..

    Cell Differentiation:

    Article Title: Targeted development of specific biomarkers of endometrial stromal cell differentiation using bioinformatics: the IFITM1 model.
    Article Snippet: .. The bioinformatic search for new biomarkers for endometrial stromal cell differentiation began by downloading the ‘normal tissue data’ file from the Human Protein Atlas project (available at http:// proteinatlas.org/about/download). ..



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    The <t>expression</t> of GDF6 in various human <t>normal</t> <t>tissues</t> and tumor tissues. ( A ) The mRNA expression of GDF6 in normal human tissues. ( B ) GDF6 expression in tumors and healthy tissues (TCGA database). Tumor types with significantly downregulated GDF6 expression ( C ) and those with significantly upregulated expression ( D ) in the TCGA + GTEx databases. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.
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    (A &B) Contingency tables used to determine the likelihood of detecting a clinical (A) ADC and (B) CAR T target in the PDX human tumor N -glycoproteome against all other surface proteins in the human proteome. P-values were calculated using a Fisher’s exact test. (C) Normal tissue toxicity scoring system. (D) Distribution of full body normal tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Jiang et al., (left), Human Protein Atlas (middle) and GTEx RNA-seq data (right). (E) Distribution of normal brain tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Tushaus et al., (left), Human Protein Atlas brain <t>IHC</t> <t>data</t> (middle) and Human Protein Atlas brain RNA-seq data (right). (F) Distribution of normal heart tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Berg Luecke et al., (left) and Doll et al., (middle & right). (D-F) P-values from unpaired Mann-Whitney U tests.
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    Human Protein Atlas immunohistochemistry data of args in normal lung tissue and lusc tumor tissue
    Results of differentially expressed analysis on <t>ARGs</t> and enrichment analysis of DE‐ARGs. (A) A heatmap of 48 differentially expressed ARGs between <t>326</t> <t>LUSC</t> samples and 32 normal controls. Each line represents a DE‐ARG and each row means a sample. The expression levels of genes are displayed with colors in each cell (red for high and blue for low). (B) The volcano plot of differentially expressed ARGs between LUSC samples and normal controls. (C) The enriched significant KEGG signal pathways of DE‐ARGs. The color represents the statistical significance of the term. The length indicates the counts of enriched genes.
    Immunohistochemistry Data Of Args In Normal Lung Tissue And Lusc Tumor Tissue, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    The expression of GDF6 in various human normal tissues and tumor tissues. ( A ) The mRNA expression of GDF6 in normal human tissues. ( B ) GDF6 expression in tumors and healthy tissues (TCGA database). Tumor types with significantly downregulated GDF6 expression ( C ) and those with significantly upregulated expression ( D ) in the TCGA + GTEx databases. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Journal: Current Issues in Molecular Biology

    Article Title: Dual-Faced Role of GDF6 in Cancer: Mechanistic Insights into Its Context-Dependent Regulation of Metastasis and Immune Evasion Across Human Malignancies

    doi: 10.3390/cimb47040249

    Figure Lengend Snippet: The expression of GDF6 in various human normal tissues and tumor tissues. ( A ) The mRNA expression of GDF6 in normal human tissues. ( B ) GDF6 expression in tumors and healthy tissues (TCGA database). Tumor types with significantly downregulated GDF6 expression ( C ) and those with significantly upregulated expression ( D ) in the TCGA + GTEx databases. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

    Article Snippet: Normal tissue expression data were sourced from the Human Protein Atlas (HPA; https://www.proteinatlas.org , accessed on 15 February 2025).

    Techniques: Expressing

    (A &B) Contingency tables used to determine the likelihood of detecting a clinical (A) ADC and (B) CAR T target in the PDX human tumor N -glycoproteome against all other surface proteins in the human proteome. P-values were calculated using a Fisher’s exact test. (C) Normal tissue toxicity scoring system. (D) Distribution of full body normal tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Jiang et al., (left), Human Protein Atlas (middle) and GTEx RNA-seq data (right). (E) Distribution of normal brain tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Tushaus et al., (left), Human Protein Atlas brain IHC data (middle) and Human Protein Atlas brain RNA-seq data (right). (F) Distribution of normal heart tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Berg Luecke et al., (left) and Doll et al., (middle & right). (D-F) P-values from unpaired Mann-Whitney U tests.

    Journal: bioRxiv

    Article Title: Pan-cancer N -glycoproteomic atlas of patient-derived xenografts uncovers FAT2 as a therapeutic target for head and neck cancers

    doi: 10.1101/2024.12.11.627962

    Figure Lengend Snippet: (A &B) Contingency tables used to determine the likelihood of detecting a clinical (A) ADC and (B) CAR T target in the PDX human tumor N -glycoproteome against all other surface proteins in the human proteome. P-values were calculated using a Fisher’s exact test. (C) Normal tissue toxicity scoring system. (D) Distribution of full body normal tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Jiang et al., (left), Human Protein Atlas (middle) and GTEx RNA-seq data (right). (E) Distribution of normal brain tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Tushaus et al., (left), Human Protein Atlas brain IHC data (middle) and Human Protein Atlas brain RNA-seq data (right). (F) Distribution of normal heart tissue abundance or detection frequency of PDX target candidates (purple) vs solid tumor clinical immunotherapy targets (grey) in Berg Luecke et al., (left) and Doll et al., (middle & right). (D-F) P-values from unpaired Mann-Whitney U tests.

    Article Snippet: Normal tissue IHC data were downloaded from Human Protein Atlas (v.23.0) .

    Techniques: Glycoproteomics, RNA Sequencing, MANN-WHITNEY

    Results of differentially expressed analysis on ARGs and enrichment analysis of DE‐ARGs. (A) A heatmap of 48 differentially expressed ARGs between 326 LUSC samples and 32 normal controls. Each line represents a DE‐ARG and each row means a sample. The expression levels of genes are displayed with colors in each cell (red for high and blue for low). (B) The volcano plot of differentially expressed ARGs between LUSC samples and normal controls. (C) The enriched significant KEGG signal pathways of DE‐ARGs. The color represents the statistical significance of the term. The length indicates the counts of enriched genes.

    Journal: Cancer Reports

    Article Title: A Four‐Gene Autophagy‐Related Prognostic Model Signature and Its Association With Immune Phenotype in Lung Squamous Cell Carcinoma

    doi: 10.1002/cnr2.70000

    Figure Lengend Snippet: Results of differentially expressed analysis on ARGs and enrichment analysis of DE‐ARGs. (A) A heatmap of 48 differentially expressed ARGs between 326 LUSC samples and 32 normal controls. Each line represents a DE‐ARG and each row means a sample. The expression levels of genes are displayed with colors in each cell (red for high and blue for low). (B) The volcano plot of differentially expressed ARGs between LUSC samples and normal controls. (C) The enriched significant KEGG signal pathways of DE‐ARGs. The color represents the statistical significance of the term. The length indicates the counts of enriched genes.

    Article Snippet: Immunohistochemistry data of ARGs in normal lung tissue and LUSC tumor tissue from The Human Protein Atlas project are also included (Figure ).

    Techniques: Expressing