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Research 181–210 of 1000+
- A simple and rapid model for hair-follicle regeneration in the nude mouse
- A Simple Method to Extract DNA from Hair Shafts Using Enzymatic Laundry Powder
- Assessment of rate of hair growth using a simple trichometer
- A simple technique to distinguish fibrosing alopecia in a pattern distribution from androgenetic alopecia and concomitant seborrheic dermatitis
- A simple and low-cost environmental enrichment program improves the welfare of Calomys callosus, a species that adapts to animal facilities
- A Simple Decision Tree Suited for Identification of Early Oral Drug Candidates With Likely Pharmacokinetic Nonlinearity by Intestinal CYP3A Saturation
- A Simple Assessing Method for Screening Prevalence of Polycystic Ovary Syndrome (The Thief of Womanhood) and Emotional Distress in Female Students at Northern Border University (NBU) in Arar, Kingdom of Saudi Arabia (KSA)
- A simple method to visualize the regrowth of white vellus hairs using superficial cryotherapy
- Faculty Opinions recommendation of Distinguishing androgenetic alopecia from chronic telogen effluvium when associated in the same patient: a simple noninvasive method.
- Faculty Opinions recommendation of Distinguishing androgenetic alopecia from chronic telogen effluvium when associated in the same patient: a simple noninvasive method.
- Faculty Opinions recommendation of Distinguishing androgenetic alopecia from chronic telogen effluvium when associated in the same patient: a simple noninvasive method.
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Cepharanthine Suppresses Herpes Simplex Virus Type 1 Replication Through the Downregulation of the PI3K/Akt and p38 MAPK Signaling Pathways
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- Diffuse partial woolly hair in a patient with epidermolysis bullosa simplex with mottled pigmentation
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.