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Research 271–300 of 1000+
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- The Clinical Presentation of Systemic Lupus Erythematosus
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Liposomal systems as drug delivery vehicles for dermal and transdermal applications
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Hair Follicles: Strategic Targets for Promoting Hair Growth
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Hashimoto Thyroiditis - A Comprehensive Review
- Fertility and Sterility Vol 101 No 4, April 2014
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Siberian cats help in solving part of the mystery surrounding golden cats
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Generalized atrophic benign epidermolysis bullosa.
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Skin precancer.
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Keratin disorders: from gene to therapy
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- FOXN1 deficient nude severe combined immunodeficiency
- 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