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1-anilino-8-naphthalenesulfonate and Alopecia

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.

Research Excerpts

ExcerptRelevanceReference
" This natural product was only slightly toxic to Sprague-Dawley rats following a single sc injection: the LD50 was 5."1.27Toxicity and pharmacokinetics of the nonprotein amino acid L-canavanine in the rat. ( Rosenthal, GA; Thomas, DA, 1987)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (85.71)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yoshizawa, M1
Nakamura, M1
Farooq, M1
Inoue, A1
Aoki, J1
Shimomura, Y1
Liu, LH1
Wang, JW1
Chen, G1
Chang, RX1
Zhou, Y1
Tang, HY1
Zhu, J1
Wang, PG1
Yang, S1
Zhang, XJ1
Kalsoom, UE1
Habib, R1
Khan, B1
Ali, G2
Ali, N1
Ansar, M1
Ahmad, W1
Dereure, O1
Suga, H1
Tsunemi, Y1
Sugaya, M1
Shinkuma, S1
Akiyama, M1
Shimizu, H1
Sato, S1
Thomas, DA1
Rosenthal, GA1

Reviews

2 reviews available for 1-anilino-8-naphthalenesulfonate and Alopecia

ArticleYear
[Genodermatosis affecting the hair: new light on well-known entities].
    Annales de dermatologie et de venereologie, 2010, Volume: 137, Issue:1

    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.
    Acta dermato-venereologica, 2011, Volume: 91, Issue:4

    Topics: Alopecia; Child, Preschool; DNA Mutational Analysis; Genetic Predisposition to Disease; Hair Follicl

2011

Other Studies

5 other studies available for 1-anilino-8-naphthalenesulfonate and Alopecia

ArticleYear
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.
    Journal of dermatological science, 2013, Volume: 72, Issue:1

    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.
    The Journal of dermatology, 2014, Volume: 41, Issue:1

    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.
    Acta dermato-venereologica, 2010, Volume: 90, Issue:1

    Topics: Alopecia; Asian People; DNA Mutational Analysis; Genetic Predisposition to Disease; Humans; Lipase;

2010
Hereditary alopecia in Pakistani families.
    JPMA. The Journal of the Pakistan Medical Association, 2010, Volume: 60, Issue:10

    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.
    Toxicology and applied pharmacology, 1987, Volume: 91, Issue:3

    Topics: Alopecia; Amylases; Animals; Animals, Newborn; Biological Availability; Body Weight; Canavanine; Dig

1987