Search
for
Sort by
Research 31–60 of 1000+
- 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
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- Molecular genetics of androgen insensitivity
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Male-pattern baldness susceptibility locus at 20p11
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management