1-anilino-8-naphthalenesulfonate has been researched along with Hair Diseases in 26 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.
Hair Diseases: Diseases affecting the orderly growth and persistence of hair.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The severity of hypotrichosis is known to be able to change in the clinical course, and the mutation patterns of LIPH do not always correlate with the severity of hypotrichosis in ARWH caused by other mutation sites of LIPH." | 1.39 | Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood. ( Akiyama, M; Shimizu, H; Shinkuma, S; Sugiura, K; Takama, H; Takeichi, T; Tanahashi, K, 2013) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 22 (84.62) | 24.3611 |
| 2020's | 4 (15.38) | 2.80 |
| Authors | Studies |
|---|---|
| Hayashi, R | 5 |
| Shimomura, Y | 10 |
| Taki, T | 2 |
| Tanahashi, K | 4 |
| Takeichi, T | 3 |
| Yoshikawa, T | 1 |
| Murase, Y | 1 |
| Sugiura, K | 4 |
| Akiyama, M | 6 |
| Lv, H | 1 |
| Li, M | 1 |
| Cheng, R | 1 |
| Ahmad, F | 1 |
| Sharif, S | 1 |
| Furqan Ubaid, M | 1 |
| Shah, K | 1 |
| Khan, MN | 1 |
| Umair, M | 1 |
| Azeem, Z | 1 |
| Ahmad, W | 2 |
| Chang, XD | 1 |
| Gu, YJ | 1 |
| Dai, S | 1 |
| Chen, XR | 1 |
| Zhang, CL | 1 |
| Zhao, HS | 1 |
| Song, QH | 1 |
| Mizukami, Y | 1 |
| Tsuruta, D | 1 |
| Sugawara, K | 1 |
| Asano, N | 1 |
| Okita, T | 1 |
| Yasuno, S | 1 |
| Yamaguchi, M | 1 |
| Kashiwagi, K | 1 |
| Kanekura, T | 1 |
| Harada, K | 1 |
| Inozume, T | 1 |
| Kawamura, T | 1 |
| Shibagaki, N | 1 |
| Kinoshita, T | 1 |
| Deguchi, N | 1 |
| Shimada, S | 1 |
| Yoshizawa, M | 1 |
| Nakamura, M | 2 |
| Farooq, M | 2 |
| Inoue, A | 2 |
| Aoki, J | 2 |
| Kono, M | 2 |
| Takama, H | 2 |
| Hamajima, N | 1 |
| Akasaka, T | 1 |
| Ito, M | 2 |
| Inui, S | 1 |
| Ito, T | 1 |
| Tokura, Y | 1 |
| Sleiman, MB | 2 |
| Abbas, O | 1 |
| Btadini, W | 1 |
| Najjar, T | 1 |
| Tofaili, M | 1 |
| Chedraoui, A | 1 |
| Khalil, S | 1 |
| Kibbi, AG | 1 |
| Kurban, M | 2 |
| Matsuo, Y | 1 |
| Tanaka, A | 1 |
| Hide, M | 1 |
| Kinoshita-Ise, M | 1 |
| Kubo, A | 1 |
| Sasaki, T | 1 |
| Umegaki-Arao, N | 1 |
| Amagai, M | 1 |
| Ohyama, M | 1 |
| Itoh, E | 1 |
| Nakahara, T | 1 |
| Furumura, M | 1 |
| Furue, M | 1 |
| Dereure, O | 1 |
| Yoshimasu, T | 1 |
| Kanazawa, N | 1 |
| Kambe, N | 1 |
| Furukawa, F | 1 |
| Khan, S | 1 |
| Habib, R | 1 |
| Mir, H | 1 |
| Naz, G | 1 |
| Ayub, M | 1 |
| Shafique, S | 1 |
| Yamin, T | 1 |
| Ali, N | 1 |
| Basit, S | 1 |
| Wasif, N | 1 |
| Kamran-Ul-Hassan Naqvi, S | 1 |
| Ali, G | 1 |
| Wali, A | 1 |
| Ansar, M | 1 |
| Shah, SH | 1 |
| Abid, A | 1 |
| Shahid, S | 1 |
| Khaliq, S | 1 |
| Wajid, M | 1 |
| Christiano, AM | 1 |
| Shinkuma, S | 2 |
| Shimizu, H | 2 |
| Nishie, W | 1 |
| Natsuga, K | 1 |
| Ujiie, H | 1 |
| Nomura, T | 1 |
| Abe, R | 1 |
4 reviews available for 1-anilino-8-naphthalenesulfonate and Hair Diseases
| Article | Year |
|---|---|
Update of recent findings in genetic hair disorders.
Topics: Genes, Recessive; Hair; Hair Diseases; Humans; Hypotrichosis; Japan; Lipase; Mutation; Pedigree | 2022 |
Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies.
Topics: Genes, Recessive; Hair; Hair Diseases; Humans; Hypotrichosis; Lipase; Mutation; Pedigree; Phenotype; | 2021 |
Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review.
Topics: Child, Preschool; Codon, Nonsense; DNA Mutational Analysis; Frameshift Mutation; Hair; Hair Diseases | 2018 |
[Genodermatosis affecting the hair: new light on well-known entities].
Topics: Alopecia; Animals; Hair Diseases; Humans; Hypertrichosis; Lipase; Mice; Mice, Hairless; Receptors, P | 2010 |
1 trial available for 1-anilino-8-naphthalenesulfonate and Hair Diseases
| Article | Year |
|---|---|
Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by LIPH Pathogenic Variants.
Topics: Administration, Topical; Adolescent; Child; Child, Preschool; Female; Hair; Hair Diseases; Hair Foll | 2020 |
21 other studies available for 1-anilino-8-naphthalenesulfonate and Hair Diseases
| Article | Year |
|---|---|
Novel small-insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis.
Topics: Adult; Female; Genes, Recessive; Hair; Hair Diseases; Humans; Hypotrichosis; Lipase; Mutagenesis, In | 2020 |
Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families.
Topics: Adolescent; Adult; Base Sequence; Consanguinity; DNA Mutational Analysis; Family; Female; Gene Expre | 2018 |
Novel mutations in the lipase H gene lead to secretion defects of LIPH in Chinese patients with autosomal recessive woolly hair/hypotrichosis (ARWH/HT).
Topics: Amino Acid Sequence; Asian People; Autoantigens; Base Sequence; Child; Child, Preschool; Female; Gen | 2017 |
Identification of a novel splice site mutation in the LIPH gene in a Japanese family with autosomal recessive woolly hair.
Topics: Asian People; DNA Mutational Analysis; Female; Genetic Testing; Hair; Hair Diseases; HEK293 Cells; H | 2019 |
Two cases of autosomal recessive woolly hair with LIPH gene mutations.
Topics: Child; Hair; Hair Diseases; Homozygote; Humans; Lipase; Male; Mutation; Sequence Analysis, DNA | 2013 |
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 |
Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations.
Topics: Asian People; DNA Primers; Founder Effect; Gene Frequency; Genetics, Population; Genotype; Hair; Hai | 2014 |
Compound heterozygous mutations in two distinct catalytic residues of the LIPH gene underlie autosomal recessive woolly hair in a Japanese family.
Topics: Adolescent; Asian People; Catalytic Domain; Child; Female; Hair Diseases; Heterozygote; Humans; Japa | 2014 |
Expression studies of a novel splice site mutation in the LIPH gene identified in a Japanese patient with autosomal recessive woolly hair.
Topics: Child; DNA Mutational Analysis; Hair Diseases; Heterozygote; Humans; Japan; Lipase; Male; Mutation; | 2014 |
Identification of a novel mutation, c.686delAins18 (p.Asp229Glyfs*22), in the LIPH gene as a compound heterozygote with c.736T>A (p.Cys246Ser) in autosomal recessive woolly hair/hypotrichosis.
Topics: Alleles; Case-Control Studies; Child; Child, Preschool; Female; Hair; Hair Diseases; Heterozygote; H | 2015 |
Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis.
Topics: Child; Codon, Nonsense; Hair; Hair Diseases; Humans; Hypotrichosis; Lipase; Male | 2015 |
Novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair.
Topics: Asian People; Child, Preschool; Hair; Hair Diseases; Humans; Japan; Lipase; Male; Mutation; RNA Spli | 2016 |
Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation.
Topics: Adult; Child; Child, Preschool; Dermoscopy; Female; Hair; Hair Diseases; Hair Preparations; Homozygo | 2017 |
Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan.
Topics: Adolescent; Adult; Child; Child, Preschool; Female; Founder Effect; Hair; Hair Diseases; Humans; Hyp | 2017 |
Case of autosomal recessive woolly hair/hypotrichosis with atopic dermatitis.
Topics: Child, Preschool; Comorbidity; Dermatitis, Atopic; DNA Mutational Analysis; Female; Filaggrin Protei | 2017 |
Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair.
Topics: Alleles; Amino Acid Substitution; Asian People; Base Sequence; Child; Child, Preschool; DNA Mutation | 2011 |
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.
Topics: Adult; Child; Consanguinity; DNA Mutational Analysis; Exons; Female; Genes, Recessive; Genetic Linka | 2011 |
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.
Topics: Adult; Base Sequence; Consanguinity; Cross-Sectional Studies; Female; Genetic Linkage; Genetic Predi | 2011 |
Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis.
Topics: Female; Hair Diseases; Haplotypes; Humans; Hypotrichosis; Lipase; Male; Mutation; Pedigree; Receptor | 2013 |
Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood.
Topics: Adult; Asian People; Child, Preschool; Female; Hair; Hair Diseases; Humans; Hypotrichosis; Lipase; M | 2013 |
The β9 loop domain of PA-PLA1α has a crucial role in autosomal recessive woolly hair/hypotrichosis.
Topics: Base Sequence; Child, Preschool; Female; Genes, Recessive; Hair Diseases; HEK293 Cells; Humans; Hydr | 2012 |