OpenURL Connection Search

Select item for more details and to access through your institution.

Comparison of Intracellular Transcriptional Response of NHBE Cells to Infection with SARS-CoV-2 Washington and New York Strains.
Published in:
Frontiers in Cellular & Infection Microbiology, 2022, v. 12, p. 1, doi. 10.3389/fcimb.2022.1009328
By:
- Scott, Tiana M.;
- Solis-Leal, Antonio;
- Lopez, J. Brandon;
- Robison, Richard A.;
- Berges, Bradford K.;
- Pickett, Brett E.
Publication type:
Article
RERE deficiency contributes to the development of orofacial clefts in humans and mice.
Published in:
Human Molecular Genetics, 2021, v. 30, n. 7, p. 595, doi. 10.1093/hmg/ddab084
By:
- Kim, Bum Jun;
- Zaveri, Hitisha P;
- Kundert, Peter N;
- Jordan, Valerie K;
- Scott, Tiana M;
- Carmichael, Jenny;
- Scott, Daryl A
Publication type:
Article
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.
Published in:
Human Mutation, 2022, v. 43, n. 4, p. 461, doi. 10.1002/humu.24332
By:
- Gofin, Yoel;
- Wang, Tianyun;
- Gillentine, Madelyn A.;
- Scott, Tiana M.;
- Berry, Aliska M.;
- Azamian, Mahshid S.;
- Genetti, Casie;
- Agrawal, Pankaj B.;
- Picker, Jonathan;
- Wojcik, Monica H.;
- Delgado, Mauricio R.;
- Lynch, Sally A.;
- Scherer, Stephen W.;
- Howe, Jennifer L.;
- Bacino, Carlos A.;
- DiTroia, Stephanie;
- VanNoy, Grace E.;
- O'Donnell‐Luria, Anne;
- Lalani, Seema R.;
- Graf, William D.
Publication type:
Article
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder.
Published in:
Human Mutation, 2020, v. 41, n. 5, p. 921, doi. 10.1002/humu.23992
By:
- Scott, Tiana M.;
- Guo, Hui;
- Eichler, Evan E.;
- Rosenfeld, Jill A.;
- Pang, Kaifang;
- Liu, Zhandong;
- Lalani, Seema;
- Bi, Weimin;
- Yang, Yaping;
- Bacino, Carlos A.;
- Streff, Haley;
- Lewis, Andrea M.;
- Koenig, Mary K.;
- Thiffault, Isabelle;
- Bellomo, Allison;
- Everman, David B.;
- Jones, Julie R.;
- Stevenson, Roger E.;
- Bernier, Raphael;
- Gilissen, Christian
Publication type:
Article
Genetic Modification of Primary Human Myeloid Cells to Study Cell Migration, Activation, and Organelle Dynamics.
Published in:
Current Protocols, 2022, v. 2, n. 8, p. 1, doi. 10.1002/cpz1.514
By:
- Greiner, Daniel;
- Scott, Tiana M.;
- Olson, Gregory S.;
- Aderem, Alan;
- Roh‐Johnson, Minna;
- Johnson, Jarrod S.
Publication type:
Article

Found: 5

Comparison of Intracellular Transcriptional Response of NHBE Cells to Infection with SARS-CoV-2 Washington and New York Strains.

RERE deficiency contributes to the development of orofacial clefts in humans and mice.

Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.

BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder.

Genetic Modification of Primary Human Myeloid Cells to Study Cell Migration, Activation, and Organelle Dynamics.