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Research 511–540 of 1000+
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia
- Ugreelig hår
- Buschke-Ollendorff syndrome
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- The Naked (N) Mutation, Chromosome 15
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Colon Cancer Prevention and Its Transcriptomics‐Based Identification of Molecular Mechanisms by Dietary Intake of Soy Food
- The Case | Bilateral kidney tumors and lung cysts
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Correction of ornithine transcarbamylase (OTC) deficiency in spf‐ash mice by introduction of rat OTC gene
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Plasma levels of C19 steroid glucuronides in pre-menopausal women with non-classical congenital adrenal hyperplasia
- Claudin tight junctionwhat's your function? The role of Claudin 6 in epidermal and hair follicle differentiation
- Prolactin Signaling Influences the Timing Mechanism of the Hair Follicle: Analysis of Hair Growth Cycles in Prolactin Receptor Knockout Mice*
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Skin diseases associated with atopic dermatitis
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6