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Research 301–330 of 1000+
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- FORENSIC MEDICAL CHARACTERISTICS OF ACUTE THALLIUM POISONING AND ITS LONG-TERM EFFECTS
- Characterization of thyroid disorders in alopecia areata patients: A cross-sectional evaluation
- Quantification of biotin in plasma samples by column switching liquid chromatography – tandem mass spectrometry
- Genetics of thyroid lesions updated
- Cross-section trichometry, a clinical tool for assessing the progression and treatment response of alopecia
- British Society for Dermatopathology: Summaries of Papers
- Morphogenesis- and Hair Cycle-dependent Expression of Trichohyalin, Peptidylarginine Deiminase Type III and Deiminated Trichohyalin in Rat Dorsal Skin Hair Follicles
- WHAT OTHER JOURNALS ARE SAYING
- Microneedles as the technique of drug delivery enhancement in diverse organs and tissues
- Dermatologic manifestations of endocrine disorders
- Immediate and Delayed Complications of Dexamethasone Cyclophosphamide Pulse (DCP) Therapy
- Skin manifestations of endocrine diseases
- Endogenous steroid hormones in hair: Investigations on different hair types, pigmentation effects and correlation to nails
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Revitalizing skin, hair, nails, and muscles: Unlocking beauty and wellness with vegan collagen
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- The color of skin: white diseases of the skin, nails, and mucosa
- Autophagy Controls the Protein Composition of Hair Shafts
- Dysfunction of keratinocyte adhesion
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Building Models for Keratin Disorders
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- A Composite Model for the Transport of Hydrophilic and Lipophilic Compounds Across the Skin: Steady-State Behavior
- FOXN1 deficient nude severe combined immunodeficiency