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Research 691–720 of 1000+
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- First Symposium of Ichthyosis Experts
- Current Genetics in Hair Diseases
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Understanding Type 3 Innate Lymphoid Cells and Crosstalk with the Microbiota: A Skin Connection
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- 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
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Clinical biochemistry of dihydrotestosterone
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Study of the Thyroid Profile of Patients with Alopecia
- Improving human forensics through advances in genetics, genomics and molecular biology
- Polycystic ovary syndrome
- Intracrine androgen biosynthesis, metabolism and action revisited
- Polycystic Ovary Syndrome: An Updated Overview Foregrounding Impacts of Ethnicities and Geographic Variations
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- A Global Survey of Ethnic Indian Women Living with Polycystic Ovary Syndrome: Co-Morbidities, Concerns, Diagnosis Experiences, Quality of Life, and Use of Treatment Methods
- Genetic prediction of male pattern baldness based on large independent datasets
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix