A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23-Reference-Cited by-同舟云学术

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A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23

Published:1997-03-01 Issue:3 Volume:6 Page:465-472
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Wang Y.-K.,Samos C. H.,Peoples R.,Perez-Jurado L. A.,Nusse R.,Francke U.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference38 articles.

1. Natural history of Williams syndrome: Physical characteristics

2. Williams syndrome: Autosomal dominant inheritance

3. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

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1. Frizzled‐9 triggers actin polymerization and activates mechano‐transducer YAP to rescue simulated microgravity‐induced osteoblast dysfunction;The FASEB Journal;2023-08-16

2. The hidden hedgehog of the pituitary: hedgehog signaling in development, adulthood and disease of the hypothalamic-pituitary axis;Frontiers in Endocrinology;2023-07-05

3. Oral manifestations of nine individuals with Williams syndrome. A case series;Special Care in Dentistry;2023-05-27

4. Frizzled-9 activates YAP to rescue simulated microgravity induced osteoblasts dysfunction;2023-03-31

5. Wnt Pathway Extracellular Components and Their Essential Roles in Bone Homeostasis;Genes;2022-01-13

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