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Research 451–480 of 1000+
- 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
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- New familial association between ocular coloboma and loose anagen syndrome
- 4th Intercontinental Meeting of Hair Research Societies 2004 The "World of Hair"
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Effects of anticonvulsant drugs on chromosomes.
- Human Hair Keratin‐Associated Proteins (KAPs)
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Roles of steroid sulfatase in brain and other tissues
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition