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    Research 751–780 of 1000+

    1. The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71 Mammalian genome · 2010 · 75 citations
    2. Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments BMC genomics · 2014 · 65 citations
    3. Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata Journal of Investigative Dermatology · 2007 · 36 citations
    4. Clinical characteristics of polycystic ovary syndrome: investigating differences in White and South Asian women Clinical Endocrinology · 2015 · 29 citations
    5. Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed Genes · 2020 · 27 citations
    6. Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome Prenatal Diagnosis · 2004 · 25 citations
    7. Vitamin D receptor ablation alters skin architecture and homeostasis of dendritic epidermal T cells 2005 · 16 citations
    8. Free androgen index (FAI)’s relations with oxidative stress and insulin resistance in polycystic ovary syndrome Scientific Reports · 2023 · 14 citations
    9. Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes BMC Genomics · 2024 · 13 citations
    10. Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases European Journal of Human Genetics · 2019 · 7 citations
    11. Pigmentary mosaicism: An update Indian Journal of Dermatology · 2008 · 7 citations
    12. Clinical and Demographic Characteristics of Patients Diagnosed with Polycystic Ovary Syndrome: A Cross-Sectional Observational Study Türk Kadın Sağlığı ve Neonatoloji Dergisi · 2024 · 1 citations
    13. Polycystic Ovary Syndrome: Explaining the Gynecological Aspects and Treatment Options to Patients Journal of endocrinology and diabetes · 2015 · 1 citations
    14. Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14 Frontiers in Medicine · 2026
    15. THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION Wiadomości Lekarskie · 2024
    16. Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration PubMed Central · 2015
    17. The effects of sonic, desert and Indian hedgehog signalling in skin 2003
    18. Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation Cell · 1993 · 578 citations
    19. WNT Signaling in the Control of Hair Growth and Structure Developmental biology · 1999 · 271 citations
    20. Corneal Endothelial Cell Fate Is Maintained by LGR5 Through the Regulation of Hedgehog and Wnt Pathway Stem cells · 2013 · 73 citations
    21. Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice Free radical biology & medicine · 2014 · 53 citations
    22. Update on detection, morphology and fragility in pili annulati in three kindreds Journal of the European Academy of Dermatology and Venereology · 2004 · 49 citations
    23. THERAPY OF ENDOCRINE DISEASE: Treatment of hirsutism in the polycystic ovary syndrome European journal of endocrinology · 2013 · 40 citations
    24. Culture and Differentiation of Human Hair Follicle Dermal Papilla Cells in a Soft 3D Self-Assembling Peptide Scaffold Biomolecules · 2020 · 29 citations
    25. Interfacial Adipose Tissue in Systemic Sclerosis Current Rheumatology Reports · 2017 · 23 citations
    26. Transgenic rescue of desmoglein 3 null mice with desmoglein 1 to develop a syngeneic mouse model for pemphigus vulgaris Journal of Dermatological Science · 2011 · 17 citations
    27. Towards expansion of human hair follicle stem cells in vitro Cell Proliferation · 2011 · 14 citations
    28. Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance Journal of Assisted Reproduction and Genetics · 2016 · 12 citations
    29. Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene Transgenic Research · 2012 · 8 citations
    30. Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging. PubMed · 2013 · 3 citations