sulfur has been researched along with Xeroderma Pigmentosum in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (50.00) | 18.7374 |
| 1990's | 3 (37.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| DiGiovanna, JJ; Kraemer, KH; Liang, C; Menefee, E; Morris, A; Price, VH; Schiffmann, R | 1 |
| Armier, J; Benoit, A; Marionnet, C; Quilliet, X; Sarasin, A; Stary, A | 1 |
| Alapetite, C; Benoit, A; Moustacchi, E; Sarasin, A | 1 |
| Wood, RD | 1 |
| Arlett, CF; Broughton, BC; Green, S; Harcourt, SA; Lehmann, AR; Malcolm, A; Natarajan, AT; Stefanini, M; Steingrimsdottir, H; Taylor, R | 1 |
| Crovato, F; Rebora, A | 1 |
| Giorgi, R; Lagomarsini, P; Nuzzo, F; Stefanini, M | 1 |
| Arlett, CF; Borrone, C; Cordone, G; Crovato, F; Lagomarsini, P; Marinoni, S; Nuzzo, F; Stefanini, M; Trevisan, G | 1 |
1 review(s) available for sulfur and Xeroderma Pigmentosum
| Article | Year |
|---|---|
Human diseases associated with defective DNA excision repair.
Topics: Cockayne Syndrome; DNA Damage; DNA Repair; Hair Diseases; Humans; Intellectual Disability; Skin Neoplasms; Sulfur; Xeroderma Pigmentosum | 1991 |
7 other study(ies) available for sulfur and Xeroderma Pigmentosum
| Article | Year |
|---|---|
Characterization of tiger-tail banding and hair shaft abnormalities in trichothiodystrophy.
Topics: Cystine; Darier Disease; DNA Repair; Ectodermal Dysplasia; Hair; Hair Diseases; Humans; Hyperkeratosis, Epidermolytic; Ichthyosis; Microscopy, Polarization; Photosensitivity Disorders; Sensitivity and Specificity; Sulfur; Syndrome; Xeroderma Pigmentosum | 2005 |
Recovery of normal DNA repair and mutagenesis in trichothiodystrophy cells after transduction of the XPD human gene.
Topics: Cell Line, Transformed; Colony-Forming Units Assay; DNA Helicases; DNA Repair; DNA-Binding Proteins; Fibroblasts; Genetic Complementation Test; Hair Diseases; Humans; Intellectual Disability; Metabolism, Inborn Errors; Mutagenesis; Photosensitivity Disorders; Protein Biosynthesis; Proteins; Recombinant Fusion Proteins; Sulfur; Transcription Factors; Transfection; Ultraviolet Rays; Xeroderma Pigmentosum; Xeroderma Pigmentosum Group D Protein | 1996 |
The comet assay as a repair test for prenatal diagnosis of Xeroderma pigmentosum and trichothiodystrophy.
Topics: Cells, Cultured; DNA Damage; DNA Repair; Electrophoresis; Female; Fetus; Hair Diseases; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Microscopy, Fluorescence; Pregnancy; Prenatal Diagnosis; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1997 |
Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.
Topics: Cell Survival; Child; Cockayne Syndrome; DNA; DNA Repair; Hair Diseases; Humans; Intellectual Disability; Male; RNA; Sister Chromatid Exchange; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1988 |
Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome.
Topics: Hair Diseases; Humans; Photosensitivity Disorders; Sulfur; Syndrome; Xeroderma Pigmentosum | 1988 |
Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.
Topics: Cell Fusion; Cells, Cultured; DNA Repair; Fibroblasts; Genetic Complementation Test; Hair Diseases; Humans; Intellectual Disability; Photosensitivity Disorders; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1987 |
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity.
Topics: Cells, Cultured; Child; Child, Preschool; Chromosomes, Human, 13-15; DNA Damage; DNA Replication; Female; Hair; Hair Diseases; Humans; Mutation; Photosensitivity Disorders; Sulfur; Syndrome; Ultraviolet Rays; Xeroderma Pigmentosum | 1986 |