R01 NS096173/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

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Subject: R01 NS096173/NS/NINDS NIH HHS/United States[Grant - PubMed

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Year	Number of Results
2020	1
2021	3
2022	5
2023	4
2024	0

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Local Net Charge State of Collagen Triple Helix Is a Determinant of FKBP22 Binding to Collagen III.

Ishikawa Y, Bonna A, Gould DB, Farndale RW. Ishikawa Y, et al. Int J Mol Sci. 2023 Oct 13;24(20):15156. doi: 10.3390/ijms242015156. Int J Mol Sci. 2023. PMID: 37894834 Free PMC article.

PI3K block restores age-dependent neurovascular coupling defects associated with cerebral small vessel disease.

Thakore P, Yamasaki E, Ali S, Sanchez Solano A, Labelle-Dumais C, Gao X, Chaumeil MM, Gould DB, Earley S. Thakore P, et al. Proc Natl Acad Sci U S A. 2023 Aug 29;120(35):e2306479120. doi: 10.1073/pnas.2306479120. Epub 2023 Aug 22. Proc Natl Acad Sci U S A. 2023. PMID: 37607233 Free PMC article.

Faulty TRPM4 channels underlie age-dependent cerebral vascular dysfunction in Gould syndrome.

Yamasaki E, Ali S, Sanchez Solano A, Thakore P, Smith M, Wang X, Labelle-Dumais C, Gould DB, Earley S. Yamasaki E, et al. Proc Natl Acad Sci U S A. 2023 Jan 31;120(5):e2217327120. doi: 10.1073/pnas.2217327120. Epub 2023 Jan 24. Proc Natl Acad Sci U S A. 2023. PMID: 36693102 Free PMC article.

Elevated TGFβ signaling contributes to cerebral small vessel disease in mouse models of Gould syndrome.

Branyan K, Labelle-Dumais C, Wang X, Hayashi G, Lee B, Peltz Z, Gorman S, Li BQ, Mao M, Gould DB. Branyan K, et al. Matrix Biol. 2023 Jan;115:48-70. doi: 10.1016/j.matbio.2022.11.007. Epub 2022 Nov 23. Matrix Biol. 2023. PMID: 36435425 Free PMC article.

Lysyl hydroxylase 3-mediated post-translational modifications are required for proper biosynthesis of collagen α1α1α2(IV).

Ishikawa Y, Taga Y, Coste T, Tufa SF, Keene DR, Mizuno K, Tournier-Lasserve E, Gould DB. Ishikawa Y, et al. J Biol Chem. 2022 Dec;298(12):102713. doi: 10.1016/j.jbc.2022.102713. Epub 2022 Nov 17. J Biol Chem. 2022. PMID: 36403858 Free PMC article.

Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype.

Coste T, Aloui C, Petit F, Moutton S, Devisme L, Wells CF, Leboucq N, Verpillat P, Yvert M, Rivier F, Tournier-Lasserve E. Coste T, et al. Ultrasound Obstet Gynecol. 2022 Dec;60(6):805-811. doi: 10.1002/uog.26046. Ultrasound Obstet Gynecol. 2022. PMID: 35943828 Free PMC article.

Elevated TGFβ signaling contributes to ocular anterior segment dysgenesis in Col4a1 mutant mice.

Mao M, Labelle-Dumais C, Tufa SF, Keene DR, Gould DB. Mao M, et al. Matrix Biol. 2022 Jun;110:151-173. doi: 10.1016/j.matbio.2022.05.001. Epub 2022 May 4. Matrix Biol. 2022. PMID: 35525525 Free PMC article.

COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.

Coste T, Vincent-Delorme C, Stichelbout M, Devisme L, Gelot A, Deryabin I, Pelluard F, Aloui C, Leutenegger AL, Jouannic JM, Héron D, Gould DB, Tournier-Lasserve E. Coste T, et al. Prenat Diagn. 2022 May;42(5):601-610. doi: 10.1002/pd.6113. Epub 2022 Feb 20. Prenat Diagn. 2022. PMID: 35150448 Free PMC article.

Identification of fibronectin 1 as a candidate genetic modifier in a Col4a1 mutant mouse model of Gould syndrome.

Mao M, Popli T, Jeanne M, Hoff K, Sen S, Gould DB. Mao M, et al. Dis Model Mech. 2021 Apr 1;14(4):dmm048231. doi: 10.1242/dmm.048231. Epub 2021 Apr 26. Dis Model Mech. 2021. PMID: 34424299 Free PMC article.

Type I and type V procollagen triple helix uses different subsets of the molecular ensemble for lysine posttranslational modifications in the rER.

Ishikawa Y, Taga Y, Zientek K, Mizuno N, Salo AM, Semenova O, Tufa SF, Keene DR, Holden P, Mizuno K, Gould DB, Myllyharju J, Bächinger HP. Ishikawa Y, et al. J Biol Chem. 2021 Jan-Jun;296:100453. doi: 10.1016/j.jbc.2021.100453. Epub 2021 Feb 23. J Biol Chem. 2021. PMID: 33631195 Free PMC article.

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