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Research 31–60 of 1000+
- Reciprocal effects suggest maternal and extranuclear influences on fruit traits in winter squash breeding
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- Rare Gli1+ perivascular fibroblasts promote skin wound repair
- Proteomic Analysis of Single Hairs
- Polycystic Ovary Syndrome in adolescents: an update
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- The Rotterdam Study: 2016 objectives and design update
- An Overview of Alopecias
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- <i>In vivo</i> imaging of mammary epithelial cell dynamics in response to lineage-biased Wnt/β-catenin activation
- Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Genomic Analysis of Trichotillomania
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Unraveling the Comedone Switch through Single-Cell Resolution of Human Acne Lesions
- Steroidogenic factor-1 lineage origin of skin lesions in Carney complex syndrome
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Ottawa, Ontario, Canada, February 13–16, 2013
- Two Opposing Faces of Retinoic Acid: Induction of Stemness or Induction of Differentiation Depending on Cell-Type
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Androgenic alopecia: A counterproductive outcome of the anabolic effect of androgens
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Cue masking and cultural signals: Testing context-specific preferences for bald(ing) leaders