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Research 421–450 of 1000+
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Commentary 2
- Alopezien und Hypotrichosen im Kindesalter
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Epigenetic and transcriptional profiling of secondary hair follicle stem cells during cashmere growth
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Alopecia Areata with Renal Dysgenesis
- Gene Variant in Amish a Clue to Better Aging
- Viewpoint 2
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Polycystic ovary syndrome
- Biotin and biotinidase deficiency
- Adult female acne: a guide to clinical practice
- Recent advances in understanding and managing male infertility
- 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.
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Do Changes in Chromosomes Cause Aging?
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Role of insulin resistance and diet in acne
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation