1-anilino-8-naphthalenesulfonate has been researched along with Alopecia in 7 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Alopecia: Absence of hair from areas where it is normally present.
Excerpt | Relevance | Reference |
---|---|---|
" This natural product was only slightly toxic to Sprague-Dawley rats following a single sc injection: the LD50 was 5." | 1.27 | Toxicity and pharmacokinetics of the nonprotein amino acid L-canavanine in the rat. ( Rosenthal, GA; Thomas, DA, 1987) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (14.29) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 6 (85.71) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Yoshizawa, M | 1 |
Nakamura, M | 1 |
Farooq, M | 1 |
Inoue, A | 1 |
Aoki, J | 1 |
Shimomura, Y | 1 |
Liu, LH | 1 |
Wang, JW | 1 |
Chen, G | 1 |
Chang, RX | 1 |
Zhou, Y | 1 |
Tang, HY | 1 |
Zhu, J | 1 |
Wang, PG | 1 |
Yang, S | 1 |
Zhang, XJ | 1 |
Kalsoom, UE | 1 |
Habib, R | 1 |
Khan, B | 1 |
Ali, G | 2 |
Ali, N | 1 |
Ansar, M | 1 |
Ahmad, W | 1 |
Dereure, O | 1 |
Suga, H | 1 |
Tsunemi, Y | 1 |
Sugaya, M | 1 |
Shinkuma, S | 1 |
Akiyama, M | 1 |
Shimizu, H | 1 |
Sato, S | 1 |
Thomas, DA | 1 |
Rosenthal, GA | 1 |
2 reviews available for 1-anilino-8-naphthalenesulfonate and Alopecia
Article | Year |
---|---|
[Genodermatosis affecting the hair: new light on well-known entities].
Topics: Alopecia; Animals; Hair Diseases; Humans; Hypertrichosis; Lipase; Mice; Mice, Hairless; Receptors, P | 2010 |
Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.
Topics: Alopecia; Child, Preschool; DNA Mutational Analysis; Genetic Predisposition to Disease; Hair Follicl | 2011 |
5 other studies available for 1-anilino-8-naphthalenesulfonate and Alopecia
Article | Year |
---|---|
A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis.
Topics: Adult; Alopecia; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; DNA; Female; Genes, Re | 2013 |
Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient.
Topics: Alopecia; Asian People; Child; China; Homozygote; Humans; Hypotrichosis; Lipase; Male; Mutation, Mis | 2014 |
Mutations in lipase H gene underlie autosomal recessive hypotrichosis in five Pakistani families.
Topics: Alopecia; Asian People; DNA Mutational Analysis; Genetic Predisposition to Disease; Humans; Lipase; | 2010 |
Hereditary alopecia in Pakistani families.
Topics: Alopecia; Asian People; Genes, Recessive; Humans; Lipase; Mutation; Pakistan; Pedigree | 2010 |
Toxicity and pharmacokinetics of the nonprotein amino acid L-canavanine in the rat.
Topics: Alopecia; Amylases; Animals; Animals, Newborn; Biological Availability; Body Weight; Canavanine; Dig | 1987 |