Search
for

    Sort by

    Research 541–570 of 1000+

    1. Abstracts Journal of Investigative Dermatology Symposium Proceedings · 2003
    2. The Role of Vitamins and Minerals in Hair Loss: A Review Dermatology and Therapy · 2018 · 134 citations
    3. Nutritional Disorders of the Hair and Their Management 2020 · 5 citations
    4. Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report Frontiers in Medicine · 2025
    5. Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings 1995 · 124 citations
    6. The biology and genetics of curly hair Experimental Dermatology · 2017 · 65 citations
    7. Comprehensive Overview and Treatment Update on Hair Loss Journal of Cosmetics, Dermatological Sciences and Applications · 2013 · 5 citations
    8. Abstract 1835: Development of mammary hyperplasia, dysplasia, and invasive ductal carcinoma in transgenic mice expressing the 8p11 amplicon oncogene NSD3 (WHSC1L1) Cancer Research · 2017 · 1 citations
    9. Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families Human Genetics · 2010 · 40 citations
    10. Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat PloS one · 2020 · 16 citations
    11. By the way, doctor. I don't hear nearly as much about hair loss in women as in men. But I'm 65 and have watched my hair thin considerably over the past five or six years. Is there anything I can do about it? What about Rogaine? PubMed · 2003
    12. Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases Nature Genetics · 2023 · 47 citations
    13. A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response American Journal of Medical Genetics Part A · 2021 · 5 citations
    14. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report BMC Medical Genetics · 2017 · 23 citations
    15. Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy JAAD Case Reports · 2019 · 4 citations
    16. [The Netherton syndrome with alopecia and prolinuria]. PubMed · 1978 · 4 citations
    17. Congenital atrichia associated with nevus flammeus: A rare association Indian dermatology online journal · 2014 · 2 citations
    18. Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector Research Square (Research Square) · 2023
    19. Abstract 10845: Spontaneous Coronary Artery Dissection as the Primary Presentation of Ana-Negative Lupus Circulation · 2021
    20. An eruption of numerous spiny papules in a pediatric transplant patient American Journal of Transplantation · 2020
    21. A descriptive study of alopecia patterns and their relation to thyroid dysfunction International Journal of Trichology · 2013 · 22 citations
    22. MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells Viruses · 2022 · 2 citations
    23. Claves diagnósticas en displasias pilosas II 2021 · 2 citations
    24. Abstract 5202: Bone marrow-derived epithelial cells contribute to chronic skin inflammation and skin tumor formation in the mouse Cancer Research · 2012
    25. Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector Scientific Reports · 2023
    26. Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness 2021
    27. The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events. PubMed · 1998 · 44 citations
    28. Epidermal field carcinogenesis in bald-headed: An attempt at finetuning early non-invasive detection Oncology Reports · 2009 · 10 citations
    29. New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene BMC medical genetics · 2014 · 9 citations
    30. Congenital atrichia associated with situs inversus and mesocardia International journal of trichology · 2012 · 5 citations