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Research 871–900 of 1000+
- News in brief
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- 5-Alpha reductase deficiency
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Clinical Snippets
- Perspectives of Kennedy's disease
- Keratins: the hair shaft's backbone revealed
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Ichthyosis hystrix
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Clinical Snippets
- Molecular mechanisms of androgen receptor functions
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Persistent Hypoglycemia and Macrosomia in a Newborn
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
- Uncombable hair in a case of Zellweger syndrome – A new association
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Ichthyosis follicularis with alopecia and photophobia syndrome with coexisting palmoplantar keratoderma treated with acitretin
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature