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Research 511–540 of 1000+
- Matriptase-2, A Novel Suppressor of Hepcidin.
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Early Dengue Virus Infection in Human Skin: A Cycle of Inflammation and Infectivity
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- <i>Hoxc13</i> mutant mice lack external hair
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Gsdma3 is required for hair follicle differentiation in mice
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Biotinidase deficiency characterized by skin and hair findings
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study