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Research 961–990 of 1000+
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- The clock gene brain and muscle Arnt-like protein-1 (BMAL1) is involved in hair growth
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- 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
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Shh Gene Regulates the Proliferation and Apoptosis of Dermal Papilla Cells to Affect Its Differential Expression in Secondary Hair Follicle Growth Cycle of Cashmere Goats
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary 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
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Disease causing homozygous variants in the human hairless 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
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- 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
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice