salicylic acid has been researched along with Genetic Predisposition in 30 studies
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).
| Excerpt | Relevance | Reference |
|---|---|---|
| "ACC is associated with chromosomal abnormalities and 35-50 percent of the time with trisomy 13 (Patau syndrome)." | 1.56 | Multiple Aplasia Cutis Congenita Lesions of the Scalp: A Case Study. ( Whalen, M, 2020) |
| "Melanomas associated with blue nevi (MABN) or mimicking cellular blue nevi (MMCBN) represent exceptional variants of malignant cutaneous melanocytic tumors." | 1.43 | Melanomas Associated With Blue Nevi or Mimicking Cellular Blue Nevi: Clinical, Pathologic, and Molecular Study of 11 Cases Displaying a High Frequency of GNA11 Mutations, BAP1 Expression Loss, and a Predilection for the Scalp. ( Aubin, F; Balme, B; Bonniaud, B; Byrne, M; Costa, S; de la Fouchardiere, A; Dreno, B; Grange, F; Haddad, V; Lesimple, T; Mateus, C; Mortier, L; Paindavoine, S; Pissaloux, D; Thomas, L; Vergier, B, 2016) |
| "Congenital melanoma is extraordinarily rare, and 3 types have been described: transplacental metastases from the mother, de novo congenital melanoma, and melanoma occurring in association with a congenital melanocytic nevus." | 1.40 | De novo congenital melanoma: analysis of 2 cases with array comparative genomic hybridization. ( Barnhill, RL; Li, X; Low, L; Mascarenhas, L; Su, A; Zhou, S, 2014) |
| "A diagnosis of keratosis follicularis was made, which has been treated with isotretinoin." | 1.34 | Keratosis follicularis (Darier-White disease), with an unusual palmoplantar keratoderma. ( Fangman, W; Kim, C, 2007) |
| "Trichilemmal cysts (also named pilar cyst) derived from the outer root sheath of the deeper parts of the hair follicle can segregate dominantly, and are caused by a yet unknown gene." | 1.33 | Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24-p21.2 and exclusion of beta-CATENIN and MLH1. ( Eiberg, H; Hansen, C; Hansen, L; Kjaer, KW; Mohr, J; Teglbjaerg, PS, 2005) |
| "Clinical examination showed hair loss with thinning and widening of the central parting of the scalp, both in boys and girls." | 1.33 | Androgenetic alopecia in children: report of 20 cases. ( Iorizzo, M; Piraccini, BM; Tosti, A, 2005) |
| "The cutaneous pathology of Cowden's syndrome is characterized by multiple trichilemmomas." | 1.32 | Multiple inverted follicular keratoses as a presenting sign of Cowden's syndrome: case report with human papillomavirus studies. ( Nuovo, GJ; Ruhoy, SM; Thomas, D, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 14 (46.67) | 29.6817 |
| 2010's | 15 (50.00) | 24.3611 |
| 2020's | 1 (3.33) | 2.80 |
| Authors | Studies |
|---|---|
| Daroach, M | 1 |
| Dogra, S | 1 |
| Bhattacharjee, R | 1 |
| Tp, A | 1 |
| Smith, F | 1 |
| Mahajan, R | 1 |
| Mangwanda, R | 1 |
| Myburg, AA | 1 |
| Naidoo, S | 1 |
| Liu, Q | 1 |
| Yang, J | 1 |
| Zhang, S | 1 |
| Zhao, J | 1 |
| Feng, A | 1 |
| Yang, T | 1 |
| Wang, X | 2 |
| Mao, X | 1 |
| Dong, J | 1 |
| Zhu, X | 1 |
| Leung, H | 1 |
| Leach, JE | 1 |
| Liu, B | 1 |
| Sugano, S | 1 |
| Hayashi, N | 1 |
| Kawagoe, Y | 1 |
| Mochizuki, S | 1 |
| Inoue, H | 1 |
| Mori, M | 1 |
| Nishizawa, Y | 1 |
| Jiang, CJ | 1 |
| Matsui, M | 1 |
| Takatsuji, H | 1 |
| García-Neria, MA | 1 |
| Rivera-Bustamante, RF | 1 |
| Diener, AC | 1 |
| Ausubel, FM | 2 |
| Oh, IS | 1 |
| Park, AR | 1 |
| Bae, MS | 1 |
| Kwon, SJ | 1 |
| Kim, YS | 1 |
| Lee, JE | 1 |
| Kang, NY | 1 |
| Lee, S | 1 |
| Cheong, H | 1 |
| Park, OK | 1 |
| Kim, C | 1 |
| Fangman, W | 1 |
| Jagadeeswaran, G | 1 |
| Raina, S | 1 |
| Acharya, BR | 1 |
| Maqbool, SB | 1 |
| Mosher, SL | 1 |
| Appel, HM | 1 |
| Schultz, JC | 1 |
| Klessig, DF | 1 |
| Raina, R | 1 |
| Guo, X | 1 |
| Stotz, HU | 1 |
| Song, JT | 1 |
| Koo, YJ | 1 |
| Seo, HS | 1 |
| Kim, MC | 1 |
| Choi, YD | 1 |
| Kim, JH | 1 |
| Dewdney, J | 1 |
| Reuber, TL | 1 |
| Wildermuth, MC | 1 |
| Devoto, A | 1 |
| Cui, J | 1 |
| Stutius, LM | 1 |
| Drummond, EP | 1 |
| Andreassen, OA | 1 |
| Ferrante, RJ | 1 |
| Dedeoglu, A | 1 |
| Albers, DW | 1 |
| Klivenyi, P | 1 |
| Carlson, EJ | 1 |
| Epstein, CJ | 1 |
| Beal, MF | 1 |
| Whalen, M | 1 |
| Saraggi, D | 1 |
| Salmaso, R | 1 |
| Valentini, E | 1 |
| Munari, G | 1 |
| Vindigni, V | 1 |
| Rugge, M | 1 |
| Fassan, M | 1 |
| Cerroni, L | 1 |
| Malki, L | 1 |
| Sarig, O | 1 |
| Romano, MT | 1 |
| Méchin, MC | 1 |
| Peled, A | 1 |
| Pavlovsky, M | 1 |
| Warshauer, E | 1 |
| Samuelov, L | 1 |
| Uwakwe, L | 1 |
| Briskin, V | 1 |
| Mohamad, J | 1 |
| Gat, A | 1 |
| Isakov, O | 1 |
| Rabinowitz, T | 1 |
| Shomron, N | 1 |
| Adir, N | 1 |
| Simon, M | 1 |
| McMichael, A | 1 |
| Dlova, NC | 1 |
| Betz, RC | 1 |
| Sprecher, E | 1 |
| Hörer, S | 1 |
| Marrakchi, S | 1 |
| Radner, FPW | 1 |
| Zolles, G | 1 |
| Heinz, L | 1 |
| Eichmann, TO | 1 |
| Has, C | 1 |
| Salavei, P | 1 |
| Mahfoudh, N | 1 |
| Turki, H | 1 |
| Zimmer, AD | 1 |
| Fischer, J | 1 |
| Zhang, Y | 1 |
| Mijiti, J | 1 |
| Huang, C | 1 |
| Song, Y | 1 |
| Wan, Z | 1 |
| Li, R | 1 |
| Kang, X | 1 |
| Rassman, WR | 1 |
| Pak, JP | 1 |
| Kim, J | 1 |
| Cheng, YP | 1 |
| Chiu, HY | 1 |
| Hsiao, TL | 1 |
| Hsiao, CH | 1 |
| Lin, CC | 1 |
| Liao, YH | 1 |
| Su, A | 1 |
| Low, L | 1 |
| Li, X | 1 |
| Zhou, S | 1 |
| Mascarenhas, L | 1 |
| Barnhill, RL | 1 |
| Costa, S | 1 |
| Byrne, M | 1 |
| Pissaloux, D | 1 |
| Haddad, V | 1 |
| Paindavoine, S | 1 |
| Thomas, L | 1 |
| Aubin, F | 1 |
| Lesimple, T | 1 |
| Grange, F | 1 |
| Bonniaud, B | 1 |
| Mortier, L | 1 |
| Mateus, C | 1 |
| Dreno, B | 1 |
| Balme, B | 1 |
| Vergier, B | 1 |
| de la Fouchardiere, A | 1 |
| Hadravsky, L | 1 |
| Kazakov, DV | 1 |
| Stehlik, J | 1 |
| Michal, M | 1 |
| Curik, R | 1 |
| Krupa, P | 1 |
| Skalova, A | 1 |
| Kacerovska, D | 1 |
| Rajan, N | 2 |
| Trainer, AH | 2 |
| Burn, J | 2 |
| Langtry, JA | 2 |
| Ashworth, A | 1 |
| Roberts, C | 1 |
| Chapman, P | 1 |
| Schlegel, C | 1 |
| Metzler, G | 1 |
| Burgdorf, W | 1 |
| Schaller, M | 1 |
| Federici, S | 1 |
| Griffiths, D | 1 |
| Siberchicot, F | 1 |
| Chateil, JF | 1 |
| Gilbert, B | 1 |
| Lacombe, D | 1 |
| Ruhoy, SM | 1 |
| Thomas, D | 1 |
| Nuovo, GJ | 1 |
| Eiberg, H | 1 |
| Hansen, L | 1 |
| Hansen, C | 1 |
| Mohr, J | 1 |
| Teglbjaerg, PS | 1 |
| Kjaer, KW | 1 |
| Tosti, A | 1 |
| Iorizzo, M | 1 |
| Piraccini, BM | 1 |
2 reviews available for salicylic acid and Genetic Predisposition
| Article | Year |
|---|---|
Pachyonychia congenita responding favorably to a combination of surgical and medical therapies.
Topics: Administration, Topical; Combined Modality Therapy; Female; Genetic Predisposition to Disease; Human | 2019 |
Phenotype of normal hairline maturation.
Topics: Adolescent; Adult; Aging; Alopecia; Child; Female; Genetic Predisposition to Disease; Hair; Human De | 2013 |
28 other studies available for salicylic acid and Genetic Predisposition
| Article | Year |
|---|---|
Transcriptome and hormone profiling reveals Eucalyptus grandis defence responses against Chrysoporthe austroafricana.
Topics: Ascomycota; Disease Resistance; Down-Regulation; Eucalyptus; Gene Expression Profiling; Genetic Pred | 2015 |
OsGF14b Positively Regulates Panicle Blast Resistance but Negatively Regulates Leaf Blast Resistance in Rice.
Topics: Cyclopentanes; Gene Expression Regulation, Plant; Gene Silencing; Genetic Predisposition to Disease; | 2016 |
Rice OsVAMP714, a membrane-trafficking protein localized to the chloroplast and vacuolar membrane, is involved in resistance to rice blast disease.
Topics: Cell Membrane; Chloroplasts; Gene Expression Regulation, Plant; Genetic Predisposition to Disease; O | 2016 |
Characterization of Geminivirus resistance in an accession of Capsicum chinense Jacq.
Topics: Capsicum; Geminiviridae; Genetic Predisposition to Disease; Hyaluronic Acid; Plant Diseases; Plant L | 2011 |
RESISTANCE TO FUSARIUM OXYSPORUM 1, a dominant Arabidopsis disease-resistance gene, is not race specific.
Topics: Arabidopsis; Arabidopsis Proteins; Chromosome Mapping; Chromosomes, Plant; DNA, Bacterial; Fusarium; | 2005 |
Secretome analysis reveals an Arabidopsis lipase involved in defense against Alternaria brassicicola.
Topics: Alternaria; Amino Acid Motifs; Arabidopsis; Arabidopsis Proteins; Carboxylic Ester Hydrolases; Cells | 2005 |
Keratosis follicularis (Darier-White disease), with an unusual palmoplantar keratoderma.
Topics: Administration, Oral; Adult; Biopsy; Darier Disease; Diagnosis, Differential; Dose-Response Relation | 2007 |
Arabidopsis GH3-LIKE DEFENSE GENE 1 is required for accumulation of salicylic acid, activation of defense responses and resistance to Pseudomonas syringae.
Topics: Arabidopsis; Arabidopsis Proteins; Epistasis, Genetic; Genes, Plant; Genetic Predisposition to Disea | 2007 |
Defense against Sclerotinia sclerotiorum in Arabidopsis is dependent on jasmonic acid, salicylic acid, and ethylene signaling.
Topics: Alleles; Arabidopsis; Arabidopsis Proteins; Ascomycota; Cyclopentanes; Ethylenes; Gene Expression Re | 2007 |
Overexpression of AtSGT1, an Arabidopsis salicylic acid glucosyltransferase, leads to increased susceptibility to Pseudomonas syringae.
Topics: Arabidopsis; Arabidopsis Proteins; Blotting, Northern; Enzyme Activation; Gene Expression Regulation | 2008 |
Three unique mutants of Arabidopsis identify eds loci required for limiting growth of a biotrophic fungal pathogen.
Topics: Alleles; Arabidopsis; Ascomycota; Chromosome Mapping; Chromosome Segregation; Cyclopentanes; Ethylen | 2000 |
Mice with a partial deficiency of manganese superoxide dismutase show increased vulnerability to the mitochondrial toxins malonate, 3-nitropropionic acid, and MPTP.
Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; 3,4-Dihydroxyphenylacetic Acid; Animals; Carrier Prote | 2001 |
Multiple Aplasia Cutis Congenita Lesions of the Scalp: A Case Study.
Topics: Chromosome Aberrations; Ectodermal Dysplasia; Female; Genetic Predisposition to Disease; Humans; Inf | 2020 |
Pigmented trichoblastoma developed in a sebaceous nevus: HRAS mutation as a common molecular driver.
Topics: Adult; Biomarkers, Tumor; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; GTP Ph | 2017 |
Variant
Topics: Adolescent; Adult; Age of Onset; Alopecia; Black or African American; Chi-Square Distribution; Cicat | 2019 |
A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation.
Topics: Alleles; Biopsy, Needle; Epidermal Cyst; Exome Sequencing; Female; Genetic Predisposition to Disease | 2019 |
Deep dermatophytosis caused by Microsporum ferrugineum in a patient with CARD9 mutations.
Topics: Adaptive Immunity; Adult; Antifungal Agents; CARD Signaling Adaptor Proteins; Dermatomycoses; DNA Mu | 2019 |
Scalp melanoma in a woman with LEOPARD syndrome: possible implication of PTPN11 signaling in melanoma pathogenesis.
Topics: Biopsy, Needle; Female; Follow-Up Studies; Genetic Predisposition to Disease; Germ-Line Mutation; Hu | 2013 |
De novo congenital melanoma: analysis of 2 cases with array comparative genomic hybridization.
Topics: Antineoplastic Combined Chemotherapy Protocols; Biomarkers, Tumor; Biopsy; Cell Proliferation; Chemo | 2014 |
Melanomas Associated With Blue Nevi or Mimicking Cellular Blue Nevi: Clinical, Pathologic, and Molecular Study of 11 Cases Displaying a High Frequency of GNA11 Mutations, BAP1 Expression Loss, and a Predilection for the Scalp.
Topics: Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Biopsy; Comparative Genomic Hybridization; DNA Mu | 2016 |
Aggressive Extraocular Sebaceous Carcinoma of the Scalp Involving the Brain in a Patient With Muir-Torre Syndrome.
Topics: Adult; Biopsy; Brain; Carcinoma; Disease Progression; DNA Mutational Analysis; Fatal Outcome; Geneti | 2016 |
Familial cylindromatosis and brooke-spiegler syndrome: a review of current therapeutic approaches and the surgical challenges posed by two affected families.
Topics: Carcinoma, Adenoid Cystic; Carcinoma, Skin Appendage; Family; Female; Genetic Predisposition to Dise | 2009 |
Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.
Topics: Adolescent; Adult; Age Distribution; Age of Onset; Biopsy, Needle; Carcinoma, Adenoid Cystic; Child; | 2009 |
Hereditary progressive mucinous histiocytosis: first report in a male patient.
Topics: Adult; Aged; Biomarkers; Biopsy; Disease Progression; Female; Forearm; Genetic Predisposition to Dis | 2010 |
Oculo-ectodermal syndrome: a new tumour predisposition syndrome.
Topics: Alopecia; Child, Preschool; Female; Follow-Up Studies; Genetic Predisposition to Disease; Granuloma, | 2004 |
Multiple inverted follicular keratoses as a presenting sign of Cowden's syndrome: case report with human papillomavirus studies.
Topics: Breast Neoplasms; Carcinoma, Basal Cell; Carcinoma, Intraductal, Noninfiltrating; Darier Disease; DN | 2004 |
Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24-p21.2 and exclusion of beta-CATENIN and MLH1.
Topics: Adaptor Proteins, Signal Transducing; beta Catenin; Carrier Proteins; Chromosome Mapping; Chromosome | 2005 |
Androgenetic alopecia in children: report of 20 cases.
Topics: Age of Onset; Alopecia; Biopsy; Child; Dermoscopy; Female; Genetic Predisposition to Disease; Humans | 2005 |