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Research 631–660 of 1000+
- The urine as a diagnostic key for a homozygous EGFR mutation
- Hair loss in infancy and childhood
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Hair Loss in Children
- Inhibiting the cytosolic function of CXXC5 accelerates diabetic wound healing by enhancing angiogenesis and skin repair
- Beyond acne: Current aspects of sebaceous gland biology and function
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Adolescent hair loss
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world?
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Function and interactions of the Ysc84/SH3yl1 family of actin- and lipid-binding proteins
- Function of KLF4 in Stem Cell Biology
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Male pattern hair loss: Taking one for the team: The selfless gene
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles
- Regenerative medicine and hair loss: how hair follicle culture has advanced our understanding of treatment options for androgenetic alopecia
- Characteristics of flutamide action on prostatic and testicular functions in the rat
- Responses of hair follicle–associated structures to loss of planar cell polarity signaling
- The Role of Vitamins and Minerals in Hair Loss: A Review