salicylic acid has been researched along with Dwarfism in 4 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).
Dwarfism: A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height.
Excerpt | Relevance | Reference |
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" Previously, we demonstrated that the siz1 mutant, which is impaired in SUMO E3 ligase, showed a dwarf-like shoot phenotype with accumulation of salicylic acid (SA), and the expression of nahG, a bacterial salicylate hydroxylase that catabolizes SA, in siz1 reduced the SA level and suppressed dwarfism." | 3.76 | SIZ1 controls cell growth and plant development in Arabidopsis through salicylic acid. ( Hasegawa, PM; Lee, J; Miura, K; Miura, T, 2010) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Miura, K | 1 |
Lee, J | 1 |
Miura, T | 1 |
Hasegawa, PM | 1 |
Schnabel, F | 1 |
Kamphausen, SB | 1 |
Funke, R | 1 |
Kaulfuß, S | 1 |
Wollnik, B | 1 |
Zenker, M | 1 |
LaDine, BJ | 1 |
Simmons, JA | 1 |
Shrimpton, AE | 1 |
Hoo, JJ | 1 |
Boothby, CB | 1 |
Bower, BD | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
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Genetic Disease Gene Identification[NCT00916903] | 200 participants (Anticipated) | Observational | 2005-10-31 | Enrolling by invitation | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
4 other studies available for salicylic acid and Dwarfism
Article | Year |
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SIZ1 controls cell growth and plant development in Arabidopsis through salicylic acid.
Topics: Arabidopsis; Arabidopsis Proteins; Cell Differentiation; Cell Enlargement; Cell Growth Processes; Ce | 2010 |
Aplasia cutis congenita in a CDC42-related developmental phenotype.
Topics: Abnormalities, Multiple; Adult; Amino Acid Substitution; cdc42 GTP-Binding Protein; Craniofacial Abn | 2021 |
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.
Topics: Adult; Blepharoptosis; Child, Preschool; Dwarfism; Ear; Female; Guanine Nucleotide Exchange Factors; | 2001 |
Cartilage hair hypoplasia.
Topics: Bone Diseases, Developmental; Cartilage Diseases; Child, Preschool; Chromosome Aberrations; Chromoso | 1973 |