Search
for
Sort by
Research 511–540 of 1000+
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Novel cosmeceuticals from plants—An industry guided review
- Assessment of copper and zinc status in hair and urine of young women descendants of NIDDM parents
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Localization of S100A2, S100A4, S100A6, S100A7, and S100P in the human hair follicle.
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Hair phenotype diversity across Indriidae lemurs
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- AN EDUCATIONAL PACKAGE ON LESSER KNOWN HERBAL MEDICINES IN INDIA
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Chronic Alopecia
- Exploration of Therapeutic Ethno-Medicinal Plants used by Traditional Healers & Practitioners of Raichur District, Karnataka, India
- Extensive Challenges and Pending Advances in the Study of 5-Alpha-Reductase Isoenzymes. A Literature Review
- SYNTHETIC PIEZOELECTRIC POLYMERS AND THEIR APPLICATIONS IN MEDICINE; 2020-2021 OVERVIEW
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- 유전성 안드로겐탈모증의 임상적 고찰(제6보)
- Study on the distribution of hair keratin in normal hair follicles by immunohistochemical staining
- 원저 : 안드로겐성 탈모증의 임상적 고찰
- Comorbid conditions associated with androgenic alopecia: A twin study
- Very-long-chain Acyl-CoA Synthetases
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients