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Research 211–240 of 1000+
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- BJD Editor's Choice
- Registrars’ Symposium: Summaries of Papers
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Pay-For-Delay Settlements in theWake of Actavis
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- THE PATHOGENESIS OF ALOPECIA AREATA
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- <i>WNT10A</i> , dermatology and dentistry
- Ulcerative colitis and total alopecia in a mother and her son
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- WNT10B (wingless-type MMTV integration site family)
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- PCSK9: From Nature’s Loss to Patient’s Gain
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Significance of stress keratin expression in normal and diseased epithelia
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient