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Research 211–240 of 1000+
- The Roles of EDA2R in Ageing and Disease
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Androgenetic Alopecia in Men: An Update On Genetics
- Congenital Adrenal Hyperplasia
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Unrevealing the Potential of Sansevieria trifasciata Prain Fraction for the Treatment of Androgenetic Alopecia by Inhibiting Androgen Receptors Based on LC-MS/MS Analysis, and In-Silico Studies
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- BIPHENOTYPIC LEUKAEMIA
- Minoxidil oral en alopecia androgénica: estudio retrospectivo acerca de su seguridad en práctica clínica real
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Clinical Snippets
- Inherited Disorders of the Hair
- Polycystic ovary syndrome and impact on health
- The Modulatable Stem Cell Niche: Tissue Interactions during Hair and Feather Follicle Regeneration
- Hair disorders in patients with cancer
- Congenital atrichia and hypotrichosis
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- A Critical Review on Obstetric Follow-up of Women Affected by Systemic Lupus Erythematosus
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Alisertib is active as single agent in recurrent atypical teratoid rhabdoid tumors in 4 children
- British Hair and Nail Society
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Alopecia and Thyroid Disease
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep