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Research 391–420 of 1000+
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Molecular Mechanisms Regulating Hair Follicle Development
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- <i>WNT10A</i> , dermatology and dentistry
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Genetics of Structural Hair Disorders
- Nutrition and hair
- 5-Alpha reductase deficiency
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- 46,XY DSD due to impaired androgen production
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Le gène<i>hairless</i>de la souris
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Keratin disorders: from gene to therapy
- How to diagnose a lipodystrophy syndrome
- Adrenal causes of endocrine hypertension in childhood or adolescence