Search
for
Sort by
Research 31–60 of 1000+
- 354 Investigating early molecular changes in a model of x-ray radiation-induced alopecia: spotlight on growth arrest and endothelial dysfunction
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- <i>Microsporum gypseum</i> isolated from a feline case of dermatophytosis
- A microscopy-based small molecule screen in primary neurons reveals neuroprotective properties of the FDA-approved anti-viral drug Elvitegravir
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Drugs targeting epithelial–mesenchymal transition molecules for treatment of lichen planopilaris
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- Homoeopathic intervention in classic case of alopecia areata: A case study
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- The Chronic Thermal Stress Model of Androgenetic Alopecia: A Unified Environmental–Vascular–Molecular Hypothesis
- Identificación de la variación molecular y genética subyacente a las enfermedades de la piel
- Honokiol protects skin cells against inflammation, collagenolysis, apoptosis, and senescence caused by cigarette smoke damage
- Microsporum gypseum isolated from a feline case of dermatophytosis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Significance of RU58841 as a therapeutic agent effecting androgen receptor molecular interactions in human hair follicles.
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Inflammatory tinea capitis due to <i>Microsporum canis</i> transmitted from asymptomatic domestic cats
- Folliculotropic mycosis fungoides with central nervous system involvement: Demonstration of tumor clonality in intrafollicular T cells using laser capture microdissection
- Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Rapidly Progressive Alopecia Universalis after Varicella-Zoster Virus Infection: The role of Immune Dysregulation and Tofacitinib treatment
- Two females with hair loss
- Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome