Search
for
Sort by
Research 481–510 of 1000+
- Uncombable hair in a case of Zellweger syndrome – A new association
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Biotinidase deficiency characterized by skin and hair findings
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Prediction of gain-of-function and loss-of-function mutations using Combined Annotation Dependent Depletion (CADD)
- A Complex Clinical Situation in Polycystic Ovary Syndrome: HAIR‐AN Syndrome ‘‘Case Report’’
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Clinical and molecular genetic studies in hereditary hair loss
- Deletion of an enhancer in FGF5 is associated with ectopic expression in goat hair follicles and the cashmere growth phenotype
- Divergent genetic mechanism leads to spiny hair in rodents
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- From signal to form: aspects of the cytoskeleton-plasma membrane—cell wall continuuum in root hair tips
- Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother
- Genetics of thyroid lesions updated
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Towards Defining the Pathogenesis of the Hairless Phenotype
- N-terminal functional domain of Gasdermin A3 regulates mitochondrial homeostasis via mitochondrial targeting
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Defective control of growth rate and cell diameter in tip-growing root hairs of the<i>rhd4</i>mutant of<i>Arabidopsis thaliana</i>
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Early Dengue Virus Infection in Human Skin: A Cycle of Inflammation and Infectivity
- Alopecia totalis in an infant
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Abstract 4385: Live-imaging the interface between homeostasis and cancer initiation
- Editors' Picks
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS