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Research 601–630 of 1000+
- Analysis of the human diseasome using phenotype similarity between common, genetic and infectious diseases
- Androgenetic alopecia: An autosomal dominant disorder
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Regulation of stem cell function by protein ubiquitylation
- Association of Benign Prostatic Hyperplasia with Male Pattern Baldness
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Swiss Practice Recommendations for the Management of Hidradenitis Suppurativa/Acne Inversa
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Azathioprine
- Myotonic Dystrophy—A Progeroid Disease?
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Update on hidradenitis suppurativa: connecting the tracts
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Epidermolysis bullosa in animals: a review
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Erythromelanosis follicularis faciei in women
- Genetic and molecular aspects of androgenetic alopecia
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Management of Androgenetic Alopecia
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation