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Research 151–180 of 1000+
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Narrative Review of Skin and Pregnancy: Dermatologic Manifestations and Medication Management During Pregnancy
- The genetic basis of dermatophytosis skin infection susceptibility
- Divergent genetic mechanism leads to spiny hair in rodents
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Specific receptor detection by a functional keratinocyte growth factor-immunoglobulin chimera.
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Oncogenic Kras induces spatiotemporally specific tissue deformation through converting pulsatile into sustained ERK activation
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- People’s experiences of eyebrow transplantation: A qualitative study
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Identification of a Cyclosporine-Specific P450 Hydroxylase Gene through Targeted Cytochrome P450 Complement (CYPome) Disruption in Sebekia benihana
- FEATURES OF DIAGNOSIS OF POSTCOVID ALOPECIA
- Factors Driving Unique Urination Phenotypes of Male and Female 9-week-old C57BL/6J Mice
- COVID-19 infection leading to acute pustular dermatoses
- 1H NMR-based lipidomics of rodent fur: species-specific lipid profiles and SCD1 inhibitor-related dermal toxicity
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Copper Deficiency a New Reason of Androgenetic Alopecia?
- Hair shaft disorders
- Plucked hair follicles from patients with chronic discoid lupus erythematosus show a disease-specific molecular signature
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness