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Research 121–150 of 1000+
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Oncogenic senescence: a multi-functional perspective
- Programmed nanozyme hydrogel enabling spatiotemporal modulation of wound healing achieves skin regeneration after biofilm infection
- Antiandrogenic activity of Riboflavin 5′-phosphate (FMN) in 22Rv1 and LNCaP human prostate cancer cell lines
- Characteristic Localization of Neuronatin in Rat Testis, Hair Follicle, Tongue, and Pancreas
- 878 Individual variation in balance between platelet-secreted growth factors causing contradictory effects on hair follicle could potentially impact response to PRP therapy in patients with scalp hair loss
- WNT10B (wingless-type MMTV integration site family)
- 876 Imaging nanoscale changes in desmosome protein organization
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- Epidermal expression of receptor for advanced glycation end products (RAGE) is related to inflammation and apoptosis in human skin
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- The genetic basis of dermatophytosis skin infection susceptibility
- Genetic Defects of Female Sexual Differentiation
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- Expression of AKT1 along with AKT2 in granulosa-lutein cells of hyperandrogenic PCOS patients