Search
for
Sort by
Research 61–90 of 1000+
- Assessment of Human Nuclear Factor Erythroid 2 Related Factor 2 (NRF2) in Androgenetic Alopecia in Egyptian Men
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- News in brief
- Hair and nail diseases in the mature patient
- Cutaneous Manifestations of PCOS
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- 3P's (Pharmacokinetic, Pharmacodynamic, and Pharmacogenomic) of Valproate: What's New?
- Male Androgenetic Alopecia — Endotext
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic prediction of male pattern baldness
- What does acne genetics teach us about disease pathogenesis?
- Molecular Genetics of Alopecias
- Dermoscopic Assessment of Nail Alterations in Egyptian Patients with Alopecia Areata
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Polarized microscopy in genetic hair disorders: case series
- Genetic Defects of Female Sexual Differentiation
- Molecular genetics of androgen insensitivity
- Authentication of herbs by physiological & morphological studies through HPTLC, ICP-MS, UV Spectroscopy, Genetic Engineering & PCR
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency