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Research 31–60 of 1000+
- Expression Patterns of Gli-1, Pleckstrin Homology-Like Domain, Family A, Member 1, Transforming Growth Factor-β1/β2, and p63 in Sebaceous and Follicular Tumors
- Hair Restoration
- Congenital hypotrichosis due to short anagen
- Hair Restoration
- Marie-unna hereditary hypotrichosis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Inherited Disorders of the Hair
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Therapy for Alopecia Areata in Mice by Stimulating the Hair Cycle with Parathyroid Hormone Agonists Linked to a Collagen-Binding Domain
- Making the head: Caspases in life and death
- Onychomadesis associated with childhood hand-foot-mouth disease
- Hair casts
- The assessment of dermatological needs in resource‐poor regions
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Hair transplantation surgery
- Pressure alopecia
- The History of Hair Transplantation
- A non-invasive study of alopecia in Japanese macaques Macaca fuscata
- Disorders of hair in children
- A Case Report of Kaphaja Granthi w.s.r. to Trichilemmal Cyst
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- S234: Hair Transplantation and Micrografting for Oral and Maxillofacial Surgeons
- S235: Management of the Anterior Neck in Facial Rejuvenation
- S236: Mandibular Trauma: From the Simple to the Complex and Everything in Between
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers