Search
for
Sort by
Research 571–600 of 1000+
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Hair-specific expression of chloramphenicol acetyltransferase in transgenic mice under the control of an ultra-high-sulfur keratin promoter.
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Buschke-Ollendorff syndrome
- Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit
- The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the β-Arrestin Pathway
- Molecular Regulation of Melanocyte Senescence
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Alopecia Areata. Current situation and perspectives
- Analysis of lncRNAs Expression Profiles in Hair Follicle of Hu Sheep Lambskin
- Le gène<i>hairless</i>de la souris
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Androgen Receptor Polymorphisms (CAG Repeat Lengths) in Androgenetic Alopecia, Hirsutism, and Acne
- Co-operation between follicular ornithine decarboxylase and v-Ha-ras induces spontaneous papillomas and malignant conversion in transgenic skin
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Pseudofolliculitis barbae; current treatment options
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Molecular mechanisms of ectodermal dysplasia syndromes
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Autophagy and Premature Graying of Hair: The Role of LC3 as a Biomarker in a Case-Control Study
- Support for dermatological research in Sub‐Saharan Africa: insights from African hair and skin research programs
- P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma