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Research 841–870 of 1000+
- From Primary MSC Culture of Adipose Tissue to Immortalized Cell Line Producing Cytokines for Potential Use in Regenerative Medicine Therapy or Immunotherapy
- The inheritance of common baldness: Two B or not two B ?
- Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- 14-3-3σ Is Required for Club Hair Retention
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- 519 Phase I/IIa clinical trial for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Effect of calcium supplementation on bone deformity and histopathological findings of skin papules in a pediatric patient with vitamin D–dependent rickets type 2A: a case report
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- LB1007 Systemic treatment with a KLK5 inhibitor shows efficacy in a murine model of Netherton syndrome
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Emerging interactions between skin stem cells and their niches
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis
- Activation of TRPV4 Induces Exocytosis and Ferroptosis in Human Melanoma Cells
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Medication-induced hair loss: An update
- Efficacy of autogenic, allogenic and heterogenic platelet rich plasma (PRP) on Avulsion skin wounds in rabbit model