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    Research 421–450 of 1000+

    1. Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response Scientific Reports · 2017 · 7 citations
    2. A Case of Familial Male-limited Precocious Puberty with a Novel Mutation JCRPE · 2020 · 6 citations
    3. Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia Genetics and Molecular Research · 2013 · 6 citations
    4. Function of KLF4 in Stem Cell Biology InTech eBooks · 2013 · 5 citations
    5. Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor Biochemical and Biophysical Research Communications · 2020 · 4 citations
    6. Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis Amino Acids · 2024 · 3 citations
    7. How a Bird Gets Its Feathers: Insights from Chromatin Looping Developmental Cell · 2020 · 3 citations
    8. Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis Bioinformation · 2012 · 3 citations
    9. Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation Dermatologica Sinica · 2010 · 3 citations
    10. Design and development of cosmeceutical cream for hyperpigmentation and anti-aging International Journal of Advanced Community Medicine · 2018 · 2 citations
    11. Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn Cureus · 2023 · 1 citations
    12. Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family Dermatology Reports · 2011 · 1 citations
    13. 5-Alpha-reductase deficiency in a Saudi "girl" Postgraduate medical journal · 1995 · 1 citations
    14. Combined activity of selenite-resistant bacteria and Pisum sativum sprout extract against Malassezia furfur: A preliminary qualitative evaluation Lahore Garrison University Journal of Life Sciences · 2026
    15. CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy Cureus · 2026
    16. Ayurvedic Approach in Management of Vata-Kaphaja Artavdushti (PCOS) AYUSHDHARA · 2026
    17. Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant Cureus · 2025
    18. An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery Clinical Cosmetic and Investigational Dermatology · 2025
    19. Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population Molecular and Cellular Biomedical Sciences · 2025
    20. Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder OBM Genetics · 2025
    21. Atrichia congenita with papular lesions: A rare cause of pediatric alopecia TURKDERM · 2025
    22. Assessment of scalp hair survivin in patients with premature greying of hair International Journal of Dermatology Venereology and Leprosy Sciences · 2025
    23. Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing bioRxiv (Cold Spring Harbor Laboratory) · 2024
    24. Pictorial Essay on Hair Loss; the Result of Head Bones Displacement Acta Scientific Orthopaedics · 2023
    25. Polycystic Ovarian Syndrome - What is New COJ Biomedical Science & Research · 2022
    26. Coexistence of Woolly Hair and Monilethrix: A Cases Study Mağallaẗ al-Muẖtar li-l-ʿulūm · 2021
    27. Inherited Epidermolysis Bullosa: A Clinical Case Medical journal of clinical trials & case studies · 2020
    28. Alopecia Areata in 12 years old female treated with Oral Azathioprine: A case report and review Journal of Case Reports and Scientific Images · 2019
    29. WNT10B (wingless-type MMTV integration site family) Atlas of genetics and cytogenetics in oncology and haematology · 2018
    30. Phylloid terminal hair nevus: A unique clinical entity Pediatric Dermatology · 2018