Search
for
Sort by
Research 151–180 of 158
- Palatogenesis and cutaneous repair: A two‐headed coin
- Molecular characterization, expression and methylation status analysis of BMP4 gene in skin tissue of Liaoning cashmere goat during hair follicle cycle
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Rhombencephalosynapsis presenting antenatally with ventriculomegaly/hydrocephalus in a likely case of Gomez–López-Hernández syndrome
- Adverse effects of 5α-reductase inhibitors: What do we know, don’t know, and need to know?
- Molecular Genetics of Alopecias
- Alopecia in Association with Malignancy: A Review
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- <i>WNT10A</i> , dermatology and dentistry
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Biology and Genetics of Hair
- Inherited Disorders of the Hair
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Alopecia Areata with Renal Dysgenesis
- Fertility and Sterility Vol 101 No 4, April 2014
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Protoporphyrin IX: the Good, the Bad, and the Ugly