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Research 571–600 of 1000+
- Divergent genetic mechanism leads to spiny hair in rodents
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Studying Cytotoxic T-lymphocyte- Associated Antigen-4 (CTLA-4) gene Polymorphism in a Sample of Iraqi Women with Polycystic Ovarian Syndrome
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Intermediate filaments: regulation of gene expression and assembly
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- The ITGB6 gene: its role in experimental and clinical biology
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- A newborn presenting with congenital blistering
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation