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Research 30 of 1000+
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- The genetic link between thyroid dysfunction and alopecia areata: a bidirectional two-sample Mendelian randomization study
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Hormonal and Genetic Controls of Hirsutism: Link Between hyperprolactinemia, Polycystic ovary syndrome and Hirsutism
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link?
- Intrinsic factors in the pathogenesis of hidradenitis suppurativa: Genetics, hormones, and the microbiome
- 132 Genetics of Stress Hormone Concentrations in Hair of Healthy Nursery Pigs and Their Relationship with Back Test Responses
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Exploring links with rare variants, COVID-19 and short anagen hair syndrome
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- An unusual presentation of X-linked adrenoleukodystrophy
- Causal Link of Distinct Mental Disorders with Androgenetic Alopecia and Alopecia Areata: A Bidirectional Two-Sample Mendelian Randomization Study
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- A link between Androgenetic Alopecia and Aging
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Tangled Truths: Unraveling the Link Between Frontal Fibrosing Alopecia and Allergic Contact Dermatitis
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease
- PROFILE OF ALOPECIA AREATA: A QUESTIONNAIRE ANALYSIS OF PATIENT AND FAMILY
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Hair Loss in Patients with Inflammatory Bowel Disease