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Author/Creator Paria, Nandina

1. Genetic association and characterization of FSTL5 in isolated clubfoot. (26th October 2020)

Authors:
Khanshour, Anas M; Kidane, Yared H; Kozlitina, Julia; Cornelia, Reuel; Rafipay, Alexandra; De Mello, Vanessa; Weston, Mitchell; Paria, Nandina; Khalid, Aysha; Hecht, Jacqueline T; Dobbs, Matthew B; Richards, B Stephens; Vargesson, Neil; Hamra, F Kent; Wilson, Megan; Wise, Carol; Gurnett, Christin...
Journal:
Human molecular genetics
Issue:
Volume 29:Number 22(2020)
Page Start:
3717
Record Type:
Journal Article
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2. Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice. (10th May 2021)

Authors:
Rios, Jonathan J; Denton, Kristin; Russell, Jamie; Kozlitina, Julia; Ferreira, Carlos R; Lewanda, Amy F; Mayfield, Joshua E; Moresco, Eva; Ludwig, Sara; Tang, Miao; Li, Xiaohong; Lyon, Stephen; Khanshour, Anas; Paria, Nandina; Khalid, Aysha; Li, Yang; Xie, Xudong; Feng, Jian Q; Xu, Qian; Lu, Yongbo
Journal:
Journal of bone and mineral research
Issue:
Volume 36:Number 8(2021)
Page Start:
1548
Record Type:
Journal Article
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4. Neurofibromin Deficiency‐Associated Transcriptional Dysregulation Suggests a Novel Therapy for Tibial Pseudoarthrosis in NF1. (December 2014)

Authors:
Paria, Nandina; Cho, Tae‐Joon; Choi, In Ho; Kamiya, Nobuhiro; Kayembe, Kay; Mao, Rong; Margraf, Rebecca L; Obermosser, Gerlinde; Oxendine, Ila; Sant, David W; Song, Mi Hyun; Stevenson, David A; Viskochil, David H; Wise, Carol A; Kim, Harry KW; Rios, Jonathan J
Journal:
Journal of bone and mineral research
Issue:
Volume 29:Number 12(2014:Dec.)
Page Start:
2636
Record Type:
Journal Article
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