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Research 331–360 of 1000+
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Functional analysis of the PIP5K1A gene in Liaoning Cashmere goats: an investigation based on bioinformatics, tissue localization, and biological functions
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Osteopontin Gene is Expressed in the Dermal Papilla of Pelage Follicles in a Hair-Cycle-Dependent Manner
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Androgen Receptor (<i>AR</i>) Gene (CAG)n and (GGN)n Length Polymorphisms and Symptoms in Young Males With Long-Lasting Adverse Effects After Finasteride Use Against Androgenic Alopecia
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Disease causing homozygous variants in the human hairless gene
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- Comparative gene expression analysis of nestin-expressing hair follicle-derived cells
- Low Humidity Alters Epidermal Gene Expression in vivo
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women