Search
for

    Sort by

    Research 511–540 of 855

    1. Genetic disorders of keratin: are scarring alopecias a sub-set? Journal of Dermatological Science · 1994 · 14 citations
    2. Recent advances in the role of neuroregulation in skin wound healing Burns & Trauma · 2024 · 12 citations
    3. Biofunctionalization of hydrogel-based scaffolds for vascular tissue regeneration Frontiers in Materials · 2023 · 12 citations
    4. Injectable Biomimetic Gels for Biomedical Applications Biomimetics · 2024 · 11 citations
    5. Small Molecule Treatments Improve Differentiation Potential of Human Amniotic Fluid Stem Cells Frontiers in Bioengineering and Biotechnology · 2021 · 11 citations
    6. Single-Cell Sequencing Technology in Ruminant Livestock: Challenges and Opportunities Current Issues in Molecular Biology · 2024 · 5 citations
    7. Are Women with Polycystic Ovary Syndrome at Increased Risk of Alzheimer Disease? Lessons from Insulin Resistance, Tryptophan and Gonadotropin Disturbances and Their Link with Amyloid-Beta Aggregation Biomolecules · 2024 · 4 citations
    8. Impacts of Anabolic-androgenic steroid supplementation on female health and offspring: Mechanisms, side effects, and medical perspectives Saudi Pharmaceutical Journal · 2024 · 3 citations
    9. Endocrine Functions of the Testes IntechOpen eBooks · 2021 · 3 citations
    10. Anorexia nervosa and reproduction: connecting brain to gonads Journal of Mind and Medical Sciences · 2020 · 3 citations
    11. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    12. Myeloid Wls expression is dispensable for skin wound healing and blood vessel regeneration Frontiers in Endocrinology · 2022 · 2 citations
    13. Non-invasive biomonitoring of infant exposure to environmental organic pollutants in north-western Spain based on hair analysis. Identification of potential sources Environmental pollution · 2023 · 1 citations
    14. Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling Biology · 2026
    15. Microalgal Biofactories: Sustainable Solutions for Nutrition and Cosmetics Phycology · 2026
    16. Regenerative Versus Nonregenerative Repair of the Renal Medulla After Reversal of Ureteral Obstruction Seminars in Nephrology · 2025
    17. A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene Clinical Case Reports · 2025
    18. Exploring links between acne and metabolic syndrome: a narrative review Open Medicine · 2025
    19. Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development Case Reports in Genetics · 2025
    20. Proteins in Scalp Hair of Preschool Children Psych · 2024
    21. E-Poster Indian Journal of Endocrinology and Metabolism · 2023
    22. The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism Scientific Reports · 2022
    23. Author response: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis 2022
    24. Decision letter: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis 2022
    25. Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism AACE clinical case reports · 2021
    26. Prenatal and adult androgen activities in alcohol dependence Acta psychiatrica Scandinavica · 2017 · 63 citations
    27. Polycystic ovary syndrome is associated with anogenital distance, a marker of prenatal androgen exposure Human Reproduction · 2017 · 32 citations
    28. Hedonic sensitivity to natural rewards is affected by prenatal stress in a sex-dependent manner Addiction Biology · 2015 · 28 citations
    29. Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome Endocrine · 2012 · 25 citations
    30. FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis Gene · 2017 · 17 citations