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Research 871–900 of 1000+
- Colon Cancer Prevention and Its Transcriptomics‐Based Identification of Molecular Mechanisms by Dietary Intake of Soy Food
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- 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
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Prolactin Signaling Influences the Timing Mechanism of the Hair Follicle: Analysis of Hair Growth Cycles in Prolactin Receptor Knockout Mice*
- 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
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Prolactin Signaling Influences the Timing Mechanism of the Hair Follicle: Analysis of Hair Growth Cycles in Prolactin Receptor Knockout Mice
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Biotinidase deficiency characterized by skin and hair findings
- Semidominant Inheritance in Epidermolytic Ichthyosis
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Cell Polarization Defects in Early Heart Development
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- A newborn presenting with congenital blistering
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome