Search
for
Sort by
Research 961–990 of 1000+
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Herbal Extracts Induce Dermal Papilla Cell Proliferation of Human Hair Follicles
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Abstracts
- Polycystic ovary syndrome and psychological distress: Urban–rural comparison among reproductive-aged women in Bangladesh
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Cutaneous and Oral Mucosal Lesions in Cri-du-chat Syndrome
- SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- A Comment on Coronavirus Disease 2019 and the Hair
- Conditional telomerase induction causes proliferation of hair follicle stem cells
- Androgen biosynthetic pathways in the human prostate
- In vivo skin leptin modulation after 14 MeV neutron irradiation: a molecular and FT-IR spectroscopic study
- Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism
- Cell Cycle Regulation and Regeneration
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Biochemical and Histopathological Evaluation of the Radioprotective Effects of Melatonin Against Gamma Ray-Induced Skin Damage
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- An Interesting Case of Hepatic Adrenocortical Carcinoma.
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology