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Research 841–870 of 1000+
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- A review of genetic researches of and rogenic alopecia
- The Sex-Linked Histocompatibility Antigens
- SEXUAL DIMORPHISM IN MAMMALS
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Treatment of alopecia areata: “What is new on the horizon?”
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Comment on: The Gabrin sign
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- Clinical Case Notes. Tamoxifen optic neuropathy
- Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- New familial association between ocular coloboma and loose anagen syndrome
- 4th Intercontinental Meeting of Hair Research Societies 2004 The "World of Hair"
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes