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Research 361–390 of 1000+
- Hair shaft disorders: a rare case series
- Follicular Neutrophilic Inflammation (Hidradenitis Suppurativa)
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Towards a molecular understanding of hair loss and its treatment
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Management of congenital ichthyoses: European guidelines of care, part two
- Stem cells and aberrant signaling of molecular systems in skin aging
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Physiology and Medical Treatments for Alopecia
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- 157 Analysis of the hybrid schwannoma and neurofibroma including a case report of schwannomatosis caused by a mutation in the LZTR1 gene
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- 012 A Case Report of Central Centrifugal Cicatricial Alopecia in Two Generations
- Generalized atrophic benign epidermolysis bullosa.
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Trichoscopy in genetic hair shaft abnormalities
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Nilotinib-induced generalized keratosis pilaris: Report of a rare case
- Genetics of Alopecia