Search
for
Sort by
Research 631–660 of 1000+
- Claves diagnósticas en displasias pilosas II
- Abstract 5202: Bone marrow-derived epithelial cells contribute to chronic skin inflammation and skin tumor formation in the mouse
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Congenital atrichia associated with situs inversus and mesocardia
- Congenital atrichia with papular lesions
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Sex Hormones and Related Compounds, Including Hormonal Contraceptives
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Animals in Dermatology
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Alopecia Universalis Associated with Ulcerative Colitis and The Role of Azathioprine
- The anatomical distribution of lentiginous melanoma (lentigo maligna and lentigo maligna melanoma): Differences according to sex
- Patient Satisfaction and Quality of Life Among Adult Women with Androgenetic Alopecia Using 5% Topical Minoxidil.
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Value of dermoscopy for the diagnosis of monilethrix
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Use of fluorescent light energy for the management of bacterial skin infection associated with canine calcinosis cutis lesions