Mustacich D - Search Results

1

Non-contrast MR lymphography of rare lymphatic abnormalities.

Seckeler MD, Moedano L, Mustacich D, Kalb BT, Saranathan M, Galons JP, Witte MH. Seckeler MD, et al. Among authors: mustacich d. Lymphology. 2020;53(3):136-140. Lymphology. 2020. PMID: 33350287

2

Whole-body lymphangioscintigraphy and SPECT/CT in children with lymphatic complications after surgery for complex congenital heart disease.

Kuo PH, Barber BJ, Kylat RI, Klewer SE, Behan S, Lau-Braunhut S, Bernas MJ, Moedano L, Bedrick AD, Mustacich DJ, Witte MH. Kuo PH, et al. Among authors: mustacich dj. Lymphology. 2019;52(4):157-165. Lymphology. 2019. PMID: 32171182

3

Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation.

Mustacich DJ, Kylat RI, Bernas MJ, Myles RJ, Jones JA, Kanady JD, Simon AM, Georgieva TG, Witte MH, Erickson RP, Pires PW. Mustacich DJ, et al. Lymphology. 2021;54(2):78-91. Lymphology. 2021. PMID: 34735753

4

Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second family.

Erickson RP, Lai LW, Mustacich DJ, Bernas MJ, Kuo PH, Witte MH. Erickson RP, et al. Among authors: mustacich dj. Clin Genet. 2019 Nov;96(5):478-482. doi: 10.1111/cge.13622. Epub 2019 Aug 23. Clin Genet. 2019. PMID: 31403174

5

Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family.

Mustacich DJ, Lai LW, Bernas MJ, Jones JA, Myles RJ, Kuo PH, Williams WH, Witte CL, Erickson RP, Witte MH. Mustacich DJ, et al. Am J Med. 2022 Feb;135(2):e31-e41. doi: 10.1016/j.amjmed.2021.09.007. Epub 2021 Oct 15. Am J Med. 2022. PMID: 34656527 Free PMC article.

6

GATA2 controls lymphatic endothelial cell junctional integrity and lymphovenous valve morphogenesis through miR-126.

Mahamud MR, Geng X, Ho YC, Cha B, Kim Y, Ma J, Chen L, Myers G, Camper S, Mustacich D, Witte M, Choi D, Hong YK, Chen H, Varshney G, Engel JD, Wang S, Kim TH, Lim KC, Srinivasan RS. Mahamud MR, et al. Among authors: mustacich d. Development. 2019 Nov 5;146(21):dev184218. doi: 10.1242/dev.184218. Development. 2019. PMID: 31582413 Free PMC article.

7

The A31P missense mutation in cardiac myosin binding protein C alters protein structure but does not cause haploinsufficiency.

van Dijk SJ, Bezold Kooiker K, Mazzalupo S, Yang Y, Kostyukova AS, Mustacich DJ, Hoye ER, Stern JA, Kittleson MD, Harris SP. van Dijk SJ, et al. Among authors: mustacich dj. Arch Biochem Biophys. 2016 Jul 1;601:133-40. doi: 10.1016/j.abb.2016.01.006. Epub 2016 Jan 9. Arch Biochem Biophys. 2016. PMID: 26777460 Free PMC article.

8

Increased skin carcinogenesis in a keratinocyte directed thioredoxin-1 transgenic mouse.

Mustacich D, Wagner A, Williams R, Bair W, Barbercheck L, Stratton SP, Bhattacharyya AK, Powis G. Mustacich D, et al. Carcinogenesis. 2004 Oct;25(10):1983-9. doi: 10.1093/carcin/bgh195. Epub 2004 May 27. Carcinogenesis. 2004. PMID: 15166090

9

Thioredoxin reductase.

Mustacich D, Powis G. Mustacich D, et al. Biochem J. 2000 Feb 15;346 Pt 1(Pt 1):1-8. Biochem J. 2000. PMID: 10657232 Free PMC article. Review.

10

The role of the redox protein thioredoxin in cell growth and cancer.

Powis G, Mustacich D, Coon A. Powis G, et al. Among authors: mustacich d. Free Radic Biol Med. 2000 Aug;29(3-4):312-22. doi: 10.1016/s0891-5849(00)00313-0. Free Radic Biol Med. 2000. PMID: 11035260 Review.

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