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Research 301–330 of 1000+
- 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
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital atrichia with papular lesions
- 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
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Phenotypic, transcriptomic, and genomic analyses reveal the spatiotemporal patterns and associated genes of coarse hair density in goats
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- (673) Seminoma in SRY-Negative 46, XX Testicular Disorder of Sex Development Presenting as Acute Abdomen: An Extremely Rare Case Report
- 651 Epigenetic regulation of macrophage activity by glutamine during wound healing
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- 921 Generation of a new rodent model of scleroderma
- Chapter 6. Darwinian Health and Other Contradictions
- Fertility and Sterility Vol 101 No 4, April 2014
- Klinefelter syndrome and chronic leg ulcers
- This Month in the Journal
- Genetics of Diabetes in Childhood
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Cutaneous signals of immune system disease