Nottoli T - Search Results

1

Rho-GTPase Activating Protein myosin MYO9A identified as a novel candidate gene for monogenic focal segmental glomerulosclerosis.

Li Q, Gulati A, Lemaire M, Nottoli T, Bale A, Tufro A. Li Q, et al. Among authors: nottoli t. Kidney Int. 2021 May;99(5):1102-1117. doi: 10.1016/j.kint.2020.12.022. Epub 2021 Jan 4. Kidney Int. 2021. PMID: 33412162 Free PMC article.

2

Disrupting the three-dimensional regulatory topology of the Pitx1 locus results in overtly normal development.

Sarro R, Kocher AA, Emera D, Uebbing S, Dutrow EV, Weatherbee SD, Nottoli T, Noonan JP. Sarro R, et al. Among authors: nottoli t. Development. 2018 Apr 9;145(7):dev158550. doi: 10.1242/dev.158550. Development. 2018. PMID: 29549111 Free PMC article.

3

[No title available]

[No authors listed] [No authors listed] PMID: 35553440

4

Mouse Embryonic Fibroblasts Isolated From Nthl1 D227Y Knockin Mice Exhibit Defective DNA Repair and Increased Genome Instability.

Marsden CG, Das L, Nottoli TP, Kathe SD, Doublié S, Wallace SS, Sweasy JB. Marsden CG, et al. DNA Repair (Amst). 2022 Jan;109:103247. doi: 10.1016/j.dnarep.2021.103247. Epub 2021 Nov 17. DNA Repair (Amst). 2022. PMID: 34826736 Free PMC article.

5

Transcription factor AP-2gamma is essential in the extra-embryonic lineages for early postimplantation development.

Auman HJ, Nottoli T, Lakiza O, Winger Q, Donaldson S, Williams T. Auman HJ, et al. Among authors: nottoli t. Development. 2002 Jun;129(11):2733-47. doi: 10.1242/dev.129.11.2733. Development. 2002. PMID: 12015300

6

Modeling uniquely human gene regulatory function via targeted humanization of the mouse genome.

Dutrow EV, Emera D, Yim K, Uebbing S, Kocher AA, Krenzer M, Nottoli T, Burkhardt DB, Krishnaswamy S, Louvi A, Noonan JP. Dutrow EV, et al. Among authors: nottoli t. Nat Commun. 2022 Jan 13;13(1):304. doi: 10.1038/s41467-021-27899-w. Nat Commun. 2022. PMID: 35027568 Free PMC article.

7

Loss of Serum Glucocorticoid-Inducible Kinase 1 SGK1 Worsens Malabsorption and Diarrhea in Microvillus Inclusion Disease (MVID).

Ahsan MK, Dos Reis DC, Barbieri A, Sumigray KD, Nottoli T, Salas PJ, Ameen NA. Ahsan MK, et al. Among authors: nottoli t. J Clin Med. 2022 Jul 19;11(14):4179. doi: 10.3390/jcm11144179. J Clin Med. 2022. PMID: 35887942 Free PMC article.

8

AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice.

Nottoli T, Hagopian-Donaldson S, Zhang J, Perkins A, Williams T. Nottoli T, et al. Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13714-9. doi: 10.1073/pnas.95.23.13714. Proc Natl Acad Sci U S A. 1998. PMID: 9811866 Free PMC article.

9

A Human MSH6 Germline Variant Associated With Systemic Lupus Erythematosus Induces Lupus-like Disease in Mice.

Meas R, Nititham J, Taylor KE, Maher S, Clairmont K, Carufe KEW, Kashgarian M, Nottoli T, Cheong A, Nagel ZD, Gaffney PM, Criswell LA, Sweasy JB. Meas R, et al. Among authors: nottoli t. ACR Open Rheumatol. 2022 Sep;4(9):760-770. doi: 10.1002/acr2.11471. Epub 2022 Jun 16. ACR Open Rheumatol. 2022. PMID: 35708944 Free PMC article.

10

Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations.

Zhao S, Mekbib KY, van der Ent MA, Allington G, Prendergast A, Chau JE, Smith H, Shohfi J, Ocken J, Duran D, Furey CG, Hao LT, Duy PQ, Reeves BC, Zhang J, Nelson-Williams C, Chen D, Li B, Nottoli T, Bai S, Rolle M, Zeng X, Dong W, Fu PY, Wang YC, Mane S, Piwowarczyk P, Fehnel KP, See AP, Iskandar BJ, Aagaard-Kienitz B, Moyer QJ, Dennis E, Kiziltug E, Kundishora AJ, DeSpenza T Jr, Greenberg ABW, Kidanemariam SM, Hale AT, Johnston JM, Jackson EM, Storm PB, Lang SS, Butler WE, Carter BS, Chapman P, Stapleton CJ, Patel AB, Rodesch G, Smajda S, Berenstein A, Barak T, Erson-Omay EZ, Zhao H, Moreno-De-Luca A, Proctor MR, Smith ER, Orbach DB, Alper SL, Nicoli S, Boggon TJ, Lifton RP, Gunel M, King PD, Jin SC, Kahle KT. Zhao S, et al. Among authors: nottoli t. Nat Commun. 2023 Nov 17;14(1):7452. doi: 10.1038/s41467-023-43062-z. Nat Commun. 2023. PMID: 37978175 Free PMC article.

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