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Research 211–240 of 1000+
- Structure and hair follicle-specific expression of genes encoding the rat high sulfur protein B2 family
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- Hereditary vitamin D rickets: a case series in a family
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Maladaptive Hypothyroidism, or The Famine Response, After Bariatric Surgery: TSH not the Gold Standard For Detection
- Discreet monilethrix: De novo mutation on the example of polish families
- Prevalence of fronto-vertex baldness and its association with family history of androgenetic alopecia in Korean men using basic and specific classification
- P‐41 Psychogenic alopecia by fur‐plucking in a family of seal‐point Siamese cats: three cases
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Validity And Reliability of The Thai Version of The Family Dermatology Life Quality Index
- Improving Awareness and Utilization of Pediatric Wig Resources Through Provider and Family Education at Children’s Hospital of Orange County
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- Study of Hair Patterns of species of Muridae Family from Amravati District, Maharashtra.
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Correlations of the onset of androgenic alopecia with family history and serum dihydrotestosterone levels in 614 female patients
- Living with long COVID and its impact on family and society: a couple's view
- A comprehensive Review of the Morphology, Phytochemistry and Medicinal Applications of Asteraceae Family Plants.
- Characteristics of the microscopic hair structure of domestic mammals from Equidae family
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Mäklare tjugofyrasju : En studie om hur mäklare lyckas kombinera arbete och familjeliv
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Molecular Evolution of The Keratin‐associated Protein Gene Family
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair (vol 8, pg 241, 2008)
- Signaling by the Platelet-Derived Growth Factor Receptor Family