lysophosphatidic acid has been researched along with Hypotrichosis in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (66.67) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ahmad, W; Ali, RH; Hassan, M; Jan, A; Muhammad, D; Rashid, S; Raza, SI | 1 |
| Shimomura, Y | 1 |
| Christiano, AM; Garzon, MC; Kristal, L; Shapiro, L; Shimomura, Y | 1 |
| Dereure, O | 1 |
| Betz, RC; Janecke, AR; Müller, M; Nöthen, MM; Oji, V; Pasternack, SM; Sprecher, E; Traupe, H; von Kügelgen, I | 1 |
| Al Aboud, K; Betz, RC; Franz, T; Hillmer, AM; Lee, YA; Molderings, GJ; Nöthen, MM; Nürnberg, P; Pasternack, SM; Ramirez, A; Rüschendorf, F; von Kügelgen, I; Voss, K | 1 |
1 review(s) available for lysophosphatidic acid and Hypotrichosis
| Article | Year |
|---|---|
Journey toward unraveling the molecular basis of hereditary hair disorders.
Topics: Amino Acid Motifs; Ectodermal Dysplasia; Hair; Hair Diseases; Hair Follicle; Humans; Hypotrichosis; Japan; Lysophospholipids; Macular Degeneration; Monilethrix; Mutation, Missense; Signal Transduction | 2016 |
5 other study(ies) available for lysophosphatidic acid and Hypotrichosis
| Article | Year |
|---|---|
In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis.
Topics: Base Sequence; Computer Simulation; Genes, Recessive; Genetic Predisposition to Disease; Humans; Hypotrichosis; Lysophospholipids; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Pedigree; Phospholipids; Protein Binding; Protein Conformation; Receptors, Lysophosphatidic Acid; Sequence Analysis, DNA; Signal Transduction | 2014 |
Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.
Topics: Amino Acid Sequence; Case-Control Studies; Child; Female; Hair; Homozygote; Humans; Hypotrichosis; Iran; Lipase; Lysophospholipids; Molecular Sequence Data; Mutation; Pedigree; Receptors, Purinergic P2; Signal Transduction | 2009 |
[Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome].
Topics: Genes, Recessive; Hair Diseases; Hypotrichosis; Lysophospholipids; Mutation; Receptors, Purinergic P2; Syndrome | 2008 |
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth.
Topics: Animals; Base Sequence; CHO Cells; Codon, Terminator; Cricetinae; Cricetulus; Frameshift Mutation; Gene Duplication; Genes, Reporter; Hair; Humans; Hypotrichosis; In Vitro Techniques; Lipase; Lysophospholipids; Molecular Sequence Data; Substrate Specificity; Transfection | 2009 |
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.
Topics: Adult; Animals; Base Sequence; Chlorocebus aethiops; Chromosome Mapping; Chromosomes, Human, Pair 13; Consanguinity; COS Cells; DNA Mutational Analysis; Family; Hair; Humans; Hypotrichosis; Lysophospholipids; Models, Biological; Pedigree; Phylogeny; Receptors, G-Protein-Coupled; Receptors, Purinergic P2; Transfection | 2008 |