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Research 301–330 of 1000+
- Sex Identification of Feather Color in Geese and the Expression of Melanin in Embryonic Dorsal Skin Feather Follicles
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Premature hair graying: a multifaceted phenomenon
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Central centrifugal cicatricial alopecia in Black men: A case series highlighting key clinical features in this cohort
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- DNA Methylation as an Epigenetic Memory Keeper during Skin Development and Regeneration
- Differentiating pulmonary lymphangioleiomyomatosis from pulmonary langerhans cell histiocytosis and Birt-Hogg-Dube syndrome
- An updated landscape of Female Pattern Hair Loss
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Placental mRNA Expression of Neurokinin B Is Increased in PCOS Pregnancies with Female Offspring
- FGF5 is a crucial regulator of hair length in humans
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- Treatment of Satoyoshi syndrome: a systematic review
- The Effects of Lower vs Higher Cell Number of Platelet-Rich Plasma (PRP) on Hair Density and Diameter in Androgenetic Alopecia (AGA): A Randomized, Double-Blinded, Placebo, Parallel-Group Half-Scalp IRB-Approved Study.