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Research 451–480 of 1000+
- Human Derived Immortalized Dermal Papilla Cells With a Constant Expression of Testosterone Receptor
- Nosocomial Intravascular Catheter Infections with Extended-spectrum Beta-lactamase-producing<i>Escherichia coli</i>in Calves after Strain Introduction from a Commercial Herd
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- Comment on: The Gabrin sign
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Index of Suspicion
- (673) Seminoma in SRY-Negative 46, XX Testicular Disorder of Sex Development Presenting as Acute Abdomen: An Extremely Rare Case Report
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Clinical Corner: Case Report Spermatozoa and Chronic Treatment with Finasteride: A TEM and FISH Study
- Genetics of Diabetes in Childhood
- Cutaneous signals of immune system disease
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Human Hair Keratin‐Associated Proteins (KAPs)
- Hair follicle-specific keratins and their diseases
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- The 5α-Recluctase System and Its Inhibitors
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Organization and Expression of Hair Follicle Genes.
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Lithium alters mitotic progression in stamen hair cells of Tradescantia in a time-dependent and reversible fashion.
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Sex-specific Difference of Hippocampal Synaptic Plasticity in Response to Sex Neurosteroids
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation