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Research 61–90 of 1000+
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Treatment of alopecia areata: “What is new on the horizon?”
- Bloom's syndrome–‐a first report from India
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Molecular basis of androgen insensitivity
- 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
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Androgen receptors and their biology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- This Month in the Journal
- 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
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- 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
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders