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Research 61–90 of 1000+
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Establishment of Tsc2-deficient rat embryonic stem cells
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A missense mutation in Lama3 causes androgen alopecia
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- The ZIP7 Gene (Slc39a7) Encodes a Zinc Transporter Involved in Zinc Homeostasis of the Golgi Apparatus
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- Keratin disorders: from gene to therapy
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- The heme-responsive PrrH sRNA regulates<i>Pseudomonas aeruginosa</i>pyochelin gene expression
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Identification of a Cyclosporine-Specific P450 Hydroxylase Gene through Targeted Cytochrome P450 Complement (CYPome) Disruption in Sebekia benihana
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Selection signatures in goats reveal a novel deletion mutant underlying cashmere yield and diameter
- Effect of cysteine‐free human fibroblast growth factor‐5s mutant ( FGF5sC93S ) on hair growth
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant