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Research 241–270 of 1000+
- Development of a simple selection protocol for optimizing the harvest of mesenchymal stem cells from explanted human umbilical cord Wharton’s jelly
- Research Techniques Made Simple: Optical Clearing and Three-Dimensional Volumetric Imaging of Skin Biopsies
- Beyond a simple marker of stress: A multiverse analysis of biopsychosocial associations with hair cortisol and cortisone
- Critical Factors in Sample Collection and Preparation for Clinical Metabolomics of Underexplored Biological Specimens
- How Rich is Platelet Rich Plasma? A Simple Preparation Method of PRP and Its Quality According to Various Classification Systems
- Going Beyond Hair: Seven Simple Actions We Can Take to Help Prevent Major Illness in Our Hair Transplant Patients
- The Clinical Observation of Simple Hairs Auto-transplantation Combined with Minoxidil Application in Patients with Hair Loss
- Development of Stable and Simple Finasteride 333-μg/mL Suspensions that Minimize Occupational Exposure.
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis 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
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- 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
- Determination of finasteride and its metabolite in urine by dispersive liquid–liquid microextraction combined with field-enhanced sample stacking and sweeping
- RETRACTED: A two‐sample Mendelian randomization study of mutual relations of six types of diets in atopic dermatitis
- 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
- Sexual desire in a sample of married Egyptian women with polycystic ovarian syndrome
- 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.
- Autosomal recessive hereditary hypotrichosis simplex: A case report