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Research 181–210 of 1000+
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- Functional and long-lived melanocytes from human pluripotent stem cells with transient ectopic expression of JMJD3
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Androgenetic Alopecia: A Review
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Silk Fibroin and Its Nanocomposites for Wound Care: A Comprehensive Review
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- 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
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- 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
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- A case of ophiasis type of alopecia areata in a patient with ring chromosome 18 syndrome
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1