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Research 571–600 of 575
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Stem Cell Therapy for Burns: Story so Far
- Decision letter: Epithelial cells supply Sonic Hedgehog to the perinatal dentate gyrus via transport by platelets
- Анализ комплекса информационных параметров, характеризующих состояние печени собак репродуктивного возраста при патологиях
- Metallothionein expression during wool follicle development in foetal sheep
- <i>De novo</i> mutations in monilethrix
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Acne Syndromes and Mosaicism
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- The Genetics of Human Skin Disease
- Congenital hair loss disorders: Rare, but not too rare
- Connexin mutations in human disease
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer