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Research 61–90 of 1000+
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Wavy changes in sinus hairs are correlated with feline leukaemia virus infection
- Hétérogénéité tumorale du cancer de la prostate et infection par le SARS-CoV2 : une relation complexe impliquant les vésicules extracellulaires et le récepteur des androgènes
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- TMPRSS2: A Key Host Factor in SARS-CoV-2 Infection and Potential Therapeutic Target
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis