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Research 121–150 of 1000+
- XX/XY chimerism in tortoiseshell tomcats – a new case and review of the literature
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells
- Androgen receptors and their biology
- Organization and Expression of Hair Follicle Genes.
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- 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.
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Do Changes in Chromosomes Cause Aging?
- 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
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- 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
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24