Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
- 1 October 2021
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 23 (10), 1889-1900
- https://doi.org/10.1038/s41436-021-01216-8
Abstract
No abstract availableFunding Information
- National Institutes of Health (R24OD026591, U01HG00794)
- Cullen Foundation
This publication has 65 references indexed in Scilit:
- Hedgehog-dependent proliferation drives modular growth during morphogenesis of a dermal boneDevelopment, 2012
- Activin and GDF11 collaborate in feedback control of neuroepithelial stem cell proliferation and fateDevelopment, 2011
- An integrative approach to ortholog prediction for disease-focused and other functional studiesBMC Bioinformatics, 2011
- Glia instruct developmental neuronal remodeling through TGF-β signalingNature Neuroscience, 2011
- Integral role of GDF‐9 and BMP‐15 in ovarian functionMolecular Reproduction and Development, 2010
- Foxg1promotes olfactory neurogenesis by antagonizingGdf11Development, 2009
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesAmerican Journal of Human Genetics, 2009
- Redundancy of myostatin and growth/differentiation factor 11 functionBMC Developmental Biology, 2009
- A two-color acid-free cartilage and bone stain for zebrafish larvaeBiotechnic & Histochemistry, 2007
- Genetic Analysis of the Roles of BMP2, BMP4, and BMP7 in Limb Patterning and SkeletogenesisPLoS Genetics, 2006