Page last updated: 2024-10-21

1-anilino-8-naphthalenesulfonate and Autosomal Chromosome Disorders

1-anilino-8-naphthalenesulfonate has been researched along with Autosomal Chromosome Disorders in 3 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.

Research Excerpts

ExcerptRelevanceReference
"Lipoatrophic panniculitis describes the panniculitides in which atrophy is a feature."1.31Lipoatrophic panniculitis and chromosome 10 abnormality. ( Harper, JI; Hoeger, P; Malone, M; Martinez, A; Palmer, R, 2000)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boccuto, L1
Abenavoli, L1
Cascio, L1
Srikanth, S1
DuPont, B1
Mitz, AR1
Rogers, RC1
Phelan, K1
Nahum, S1
Pasternack, SM1
Pforr, J1
Indelman, M1
Wollnik, B1
Bergman, R1
Nöthen, MM1
König, A1
Khamaysi, Z1
Betz, RC1
Sprecher, E1
Martinez, A1
Malone, M1
Hoeger, P1
Palmer, R1
Harper, JI1

Other Studies

3 other studies available for 1-anilino-8-naphthalenesulfonate and Autosomal Chromosome Disorders

ArticleYear
Variability in Phelan-McDermid syndrome: The impact of the PNPLA3 p.I148M polymorphism.
    Clinical genetics, 2018, Volume: 94, Issue:6

    Topics: Alleles; Amino Acid Substitution; Biomarkers; Chromosome Deletion; Chromosome Disorders; Chromosome

2018
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.
    Archives of dermatological research, 2009, Volume: 301, Issue:5

    Topics: Arabs; Child; Chromosome Disorders; Chromosomes, Human, Pair 3; DNA Mutational Analysis; Exons; Gene

2009
Lipoatrophic panniculitis and chromosome 10 abnormality.
    The British journal of dermatology, 2000, Volume: 142, Issue:5

    Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 10; Female;

2000