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Research 871–900 of 1000+
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Insertional mutation of the hairless locus on mouse Chromosome 14
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- SnapshotDx Quiz: August 2019
- Linking allergy to mercury to HLA and burning mouth syndrome
- Skin disease in pregnancy
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- Polymorphisms of OCT1 and metformin effects in Iraqi women with polycystic ovary syndrome in Karbala city
- Retinoid Metabolism Is Altered in Human and Mouse Cicatricial Alopecia
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- Cultural evolution as a possible triggering or causative factor of common baldness
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability
- Developmental Toxicity of Levo-Alpha-Acetylmethadol (LAAM) in Tolerant Rats
- Navigating Rhupus Complexity
- Navigating Rhupus Complexity
- Autoimmune polyglandular syndrome type 4 – case report
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India