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Research 751–780 of 1000+
- Women with clinically significant hirsutism always have detectable endocrinological abnormalities
- Cytostatics and immunosuppressive drugs
- Trained Immunity and Local Innate Immune Memory in the Lung
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- White piedra and pediculosis capitis in the same patient
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- 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
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- 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.
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat