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Research 301–330 of 1000+
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Situación actual de la utilización de la dermatoscopia en medicina estética
- Situación actual de la utilización de la dermatoscopia en medicina estética
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Relationship between diet, atopy, family history, and premature hair graying
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Trichobiolight: A new, effective protocol in the treatment of androgenetic alopecia and telogen effluvium
- Biological activity of novel progesterone derivatives having a bulky ester side chains at C-3
- Black dots in trichoscopy after COVID‐19. Can it be telogen effluvium?
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Stem cells and aberrant signaling of molecular systems in skin aging
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Efectos de la alteración de los niveles de allopregnanolona durante periodos críticos del neurodesarrollo en la vulnerabilidad al consumo de alcohol
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- Laparoscopic Extirpation of Adrenal Gland Ganglioneuroma Incidentally Diagnosed during Evaluation for Patchy Alopecia Areata in an Adolescent Boy
- Androgen excess: a hallmark of polycystic ovary syndrome
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Role of caffeine in the management of androgenetic alopecia
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Relative binding affinity of novel steroids to androgen receptors in hamster prostate
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Interactions of the Vitamin D Receptor with the Corepressor Hairless