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Research 151–180 of 1000+
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- A study on common clinical pattern of presentation of skin and hair changes in nutritional deficiencies associated with dietary fallacies in children 1 to 5 years of age
- Phylloid terminal hair nevus: A unique clinical entity
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Assessment of scalp hair survivin in patients with premature greying of hair
- Female pattern hair loss: A clinical, pathophysiologic, and therapeutic review
- Biotinidase deficiency characterized by skin and hair findings
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- The Use of Elongate Microbeams of X-Rays for Simulating the Effects of Cosmic Rays on Tissues: A Study of Wound Healing and Hair Follicle Regeneration
- HAIR LOSS FROM SEBUM
- 864 Catalytic-dependent and -independent activities of Polycomb repressive complex 1 differentially regulate skin stem cell specification
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Optical coherent tomography: promising in vivo measurement of hair shaft cross section
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- Hair Growth Promoting Potential of Consciousness Energy Healing Treatment in Human Dermal Papilla Cells
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Genetic Hair Disorders: A Review
- Correlation of Hair Mineral Concentrations with Insulin Resistance in Korean Males
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- Hair Keratin: Composition, Structure and Biogenesis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Neurotrichosis: Hair‐shaft Abnormalities associated with Neurological Diseases
- Superficial temporal artery flap for reconstruction of complex facial defects: A new algorithm
- Disorders of hair in infants and children other than alopecia