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Research 151–180 of 1000+
- Cutaneous signals of immune system disease
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Androgen receptors and their biology
- <i>WNT10A</i> , dermatology and dentistry
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Inherited Disorders of the Hair
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Ultraviolet-Enhanced Trichoscopy—A New Tool to Assess Pili Annulati
- Fertility and Sterility Vol 101 No 4, April 2014
- The role of vitamin D receptor mutations in the development of alopecia
- The molecular pathogenesis of Trichilemmal carcinoma
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Dermatologic care of patients with differences of sex development
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Fertility evaluation of infertile women: a committee opinion
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Molecular basis of androgen insensitivity