R01 AR064338/AR/NIAMS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2015	2
2016	1
2017	8
2019	3
2020	2
2022	1
2024	0

1

ECM-Related Myopathies and Muscular Dystrophies: Pros and Cons of Protein Therapies.

Van Ry PM, Fontelonga TM, Barraza-Flores P, Sarathy A, Nunes AM, Burkin DJ. Van Ry PM, et al. Compr Physiol. 2017 Sep 12;7(4):1519-1536. doi: 10.1002/cphy.c150033. Compr Physiol. 2017. PMID: 28915335 Review.

2

Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice.

Bugiardini E, Nunes AM, Oliveira-Santos A, Dagda M, Fontelonga TM, Barraza-Flores P, Pittman AM, Morrow JM, Parton M, Houlden H, Elliott PM, Syrris P, Maas RP, Akhtar MM, Küsters B, Raaphorst J, Schouten M, Kamsteeg EJ, van Engelen B, Hanna MG, Phadke R, Lopes LR, Matthews E, Burkin DJ. Bugiardini E, et al. J Am Heart Assoc. 2022 Dec 6;11(23):e026494. doi: 10.1161/JAHA.122.026494. Epub 2022 Nov 29. J Am Heart Assoc. 2022. PMID: 36444867 Free PMC article.

3

Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy.

Willmann R, Gordish-Dressman H, Meinen S, Rüegg MA, Yu Q, Nagaraju K, Kumar A, Girgenrath M, Coffey CBM, Cruz V, Van Ry PM, Bogdanik L, Lutz C, Rutkowski A, Burkin DJ. Willmann R, et al. J Neuromuscul Dis. 2017;4(2):115-126. doi: 10.3233/JND-170217. J Neuromuscul Dis. 2017. PMID: 28550268 Free PMC article. Review.

4

Integrin α7: a major driver and therapeutic target for glioblastoma malignancy.

Nunes AM, Barraza-Flores P, Smith CR, Burkin DJ. Nunes AM, et al. Stem Cell Investig. 2017 Dec 18;4:97. doi: 10.21037/sci.2017.12.01. eCollection 2017. Stem Cell Investig. 2017. PMID: 29359136 Free PMC article. No abstract available.

5

PTRH2 gene mutation causes progressive congenital skeletal muscle pathology.

Doe J, Kaindl AM, Jijiwa M, de la Vega M, Hu H, Griffiths GS, Fontelonga TM, Barraza P, Cruz V, Van Ry P, Ramos JW, Burkin DJ, Matter ML. Doe J, et al. Hum Mol Genet. 2017 Apr 15;26(8):1458-1464. doi: 10.1093/hmg/ddx048. Hum Mol Genet. 2017. PMID: 28175314 Free PMC article.

6

Laminin-111 protein therapy enhances muscle regeneration and repair in the GRMD dog model of Duchenne muscular dystrophy.

Barraza-Flores P, Fontelonga TM, Wuebbles RD, Hermann HJ, Nunes AM, Kornegay JN, Burkin DJ. Barraza-Flores P, et al. Hum Mol Genet. 2019 Aug 15;28(16):2686-2695. doi: 10.1093/hmg/ddz086. Hum Mol Genet. 2019. PMID: 31179490 Free PMC article.

7

Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy.

Barraza-Flores P, Bukovec KE, Dagda M, Conner BW, Oliveira-Santos A, Grange RW, Burkin DJ. Barraza-Flores P, et al. Hum Mol Genet. 2020 Aug 3;29(13):2162-2170. doi: 10.1093/hmg/ddaa104. Hum Mol Genet. 2020. PMID: 32472139 Free PMC article.

8

Human laminin-111 and laminin-211 protein therapy prevents muscle disease progression in an immunodeficient mouse model of LAMA2-CMD.

Barraza-Flores P, Hermann HJ, Bates CR, Allen TG, Grunert TT, Burkin DJ. Barraza-Flores P, et al. Skelet Muscle. 2020 Jun 4;10(1):18. doi: 10.1186/s13395-020-00235-4. Skelet Muscle. 2020. PMID: 32498713 Free PMC article.

9

Sunitinib promotes myogenic regeneration and mitigates disease progression in the mdx mouse model of Duchenne muscular dystrophy.

Fontelonga TM, Jordan B, Nunes AM, Barraza-Flores P, Bolden N, Wuebbles RD, Griner LM, Hu X, Ferrer M, Marugan J, Southall N, Burkin DJ. Fontelonga TM, et al. Hum Mol Genet. 2019 Jul 1;28(13):2120-2132. doi: 10.1093/hmg/ddz044. Hum Mol Genet. 2019. PMID: 30806670 Free PMC article.

10

Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy.

Nunes AM, Wuebbles RD, Sarathy A, Fontelonga TM, Deries M, Burkin DJ, Thorsteinsdóttir S. Nunes AM, et al. Hum Mol Genet. 2017 Jun 1;26(11):2018-2033. doi: 10.1093/hmg/ddx083. Hum Mol Genet. 2017. PMID: 28334989 Free PMC article.

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