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Research 331–360 of 1000+
- Involvement of Wnt, Eda and Shh at defined stages of sweat gland development
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Trichothiodystrophy: Current Concepts
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Telogen Effluvium: A Review
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- SkIndia Quiz 24: Itchy papules over face
- Female Androgenetic (?) Alopecia
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- FOXN1 deficient nude severe combined immunodeficiency
- Epidermal patterning and induction of different hair types during mouse embryonic development
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Nutritional Disorders of the Hair and Their Management
- GRowing an Epidermal Tumor
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Ernährungsstörungen des Haares und deren Management
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Alleviation of Severe Skin Insults Following High-Dose Irradiation with Isolated Human Fetal Placental Stromal Cells
- Subject Index
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice