The Ptch1(DL) Mouse: A New Model to Study Lambdoid Craniosynostosis and Basal Cell Nevus Syndrome-Associated Skeletal Defects
Journal Article
Overview
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Abnormalities, Multiple - Basal Cell Nevus Syndrome
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Animal Diseases - Disease Models, Animal
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Animal Population Groups - Mice, Transgenic
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Animals
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Animals, Inbred Strains - Mice, Inbred C57BL
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Biochemical Phenomena - Signal Transduction
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Biological Factors - Hedgehog Proteins
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Bone Diseases, Developmental - Basal Cell Nevus Syndrome
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Carcinoma - Basal Cell Nevus Syndrome
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Cell Physiological Phenomena - Signal Transduction
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Congenital Abnormalities - Craniosynostoses
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Congenital Abnormalities - Craniosynostoses
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Connective Tissue - Bone and Bones
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Dysostoses - Craniosynostoses
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Embryo, Mammalian
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Genetic Diseases, Inborn - Basal Cell Nevus Syndrome
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Humans
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Male
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Mice
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Mice - Mice, Inbred C57BL
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Mice - Mice, Transgenic
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Models, Animal - Disease Models, Animal
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Models, Biological - Disease Models, Animal
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Musculoskeletal Diseases - Basal Cell Nevus Syndrome
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Musculoskeletal Diseases - Craniosynostoses
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Musculoskeletal Diseases - Craniosynostoses
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Neoplasms - Basal Cell Nevus Syndrome
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Neoplasms - Basal Cell Nevus Syndrome
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Neoplasms, Basal Cell - Basal Cell Nevus Syndrome
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Peptides - Hedgehog Proteins
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Point Mutation
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Proteins - Hedgehog Proteins
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Receptors, Cell Surface
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Receptors, Cell Surface - Patched Receptors
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Receptors, Cell Surface - Patched-1 Receptor
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Skeleton - Bone and Bones
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Skull
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Stomatognathic Diseases - Basal Cell Nevus Syndrome
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Tumor Suppressor Proteins - Patched Receptors
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Tumor Suppressor Proteins - Patched-1 Receptor
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Date in CU Experts
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January 30, 2018 10:48 AM
Full Author List
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Feng W; Choi I; Clouthier DE; Niswander L; Williams T
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