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Research 61–90 of 1000+
- The Roles of EDA2R in Ageing and Disease
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- Psoriasis del cuero cabelludo etiología, diagnóstico y tratamiento
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Do Changes in Chromosomes Cause Aging?
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Prediction of male-pattern baldness from genotypes
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis