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Research 91–120 of 1000+
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Co-option of Hair Follicle Keratins into Amelogenesis Is Associated with the Evolution of Prismatic Enamel: A Hypothesis
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Editor's evaluation: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- The Proteins of Hair and Other Hard α-Keratins
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- Hair Keratin: Composition, Structure and Biogenesis
- The Proteins of Normal and Aberrant Hair Keratins
- Hard Keratin IF and Associated Proteins
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation
- WNT Signaling in Disease
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- The developmental basis of fingerprint pattern formation and variation
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Madarosis: A marker of many Maladies
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Eyebrow Loss