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Research 391–420 of 1000+
- Telogen elongation in the hair cycle of <i>ob/ob</i> mice
- Subchronic study of sperm morphology, genotoxic and mutagenic effect of Lepidium sativum seeds aqueous extract in vivo
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- High incidence of severe hand–foot syndrome during capecitabine–docetaxel combination chemotherapy
- Office Diagnosis of Hair Shaft Defects
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Genetic Analysis of Androgen Receptors in Development and Disease
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
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- To be hairless or wise?
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- The Agouti Gene in Obesity: Central and Peripheral Mechanisms, and Therapeutic Implications
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2