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Research 571–600 of 1000+
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Association of Autoimmune Regulator Gene Rs2075876 Variant, but Not Gene Expression with Alopecia Areata in Males: A Case–control Study
- Altered methylation pattern of the SRD5A2 gene in the cerebrospinal fluid of post-finasteride patients: a pilot study
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Expression analysis of proteasome maturation protein (<i>POMP</i>) gene in Liaoning Cashmere goat
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Association of Single Nucleotide Polymorphisms in the CYP19A1 Gene with Female Pattern Hair Loss in a Chinese Population
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Expression of the β-Catenin Gene in the Skin of Embryonic Geese During Feather Bud Development
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Polymorphism in the A2M gene associated with high-quality milk in Murrah buffaloes (Bubalus bubalis)
- Polymorphic CAG Repeat Numbers in the Androgen Receptor Gene of Female Pattern Hair Loss in a Han Chinese Population
- ‘Atrichosis’, a new hairless gene with cyst formation in rats
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- Effects of Guasha on histomorphology of scraped skins and on expression of calcitonin gene-related peptide and substance P in rats
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia
- Association between <i>EGF</i> and <i>EGFR</i> Gene Polymorphisms and Susceptibility to Alopecia Areata in the Korean Population
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- <i>WNT10A</i> gene variants at the root of short anagen hair syndrome
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia
- Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study
- Association of Human Beta – Defensin 1 Gene Polymorphisms with Alopecia Areata Patients