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Research 451–480 of 1000+
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- PREVALANCE OF POLYCYSTIC OVARY SYNDROME (PCOS) AND ITS PHENOTYPES: A CLINICAL ANALYSIS IN SWABI
- BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Novel insights into cardiocutaneous syndromes
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- The role of skin macrophages under conditions of stress and injury: ultraviolet irradiation and wound healing
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- Il-10 family members as novel responders to genotoxic stress
- Androgen Levels Do Not Predict PCOS Phenotypes in Adolescents and Young Adults
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Molecular genetics of androgen insensitivity
- Systemic testosterone induces structural, immunological, and sex steroid receptor changes in human XX skin
- Testosterone enantate
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Contact Dermatitis Associated with Alopecia and Hyperpigmentation
- Impact of Testosterone on Hair and Skin
- Functional analysis of thymosin beta-4 using over-expressing transgenic mice
- Weathering of the hairless scalp: a study using skin capacitance imaging and ultraviolet light-enhanced visualization
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- Histocultures and Their Use
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- The human cysteine protease cathepsin V can compensate for murine cathepsin L in mouse epidermis and hair follicles