Search
for
Sort by
Research 151–180 of 1000+
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Alopecia Areata
- The clinical spectrum of parathyroid disease
- Cicatricial alopecia
- Clinical Approach to the Patient With Alopecia
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- An Overview of Alopecias
- Congenital hypotrichosis due to short anagen
- Alopecia areata
- Keratins: the hair shaft's backbone revealed
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Molecular Genetics of Human Hair Diseases
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Dynamic expression of Runx1 in skin affects hair structure
- Eruptive vellus hair cysts: An underdiagnosed entity
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- miR-129-5p Participates in Hair Follicle Growth by Targeting HOXC13 in Rabbit
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- The Proteins of Normal and Aberrant Hair Keratins
- Molecular Mechanisms Regulating Hair Follicle Development
- Animal and in vitro Models for the Study of Hair Follicles
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children