MaKenna R Browne
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Explore the profile of MaKenna R Browne including associated specialties, affiliations and a list of published articles.
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5
Citations
10
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Recent Articles
1.
Hendrickson P, Oristian K, Browne M, Luo L, Ma Y, Cardona D, et al.
Oncogene
. 2024 Feb;
43(16):1223-1230.
PMID: 38413794
CIC::DUX4 sarcoma (CDS) is a rare but highly aggressive undifferentiated small round cell sarcoma driven by a fusion between the tumor suppressor Capicua (CIC) and DUX4. Currently, there are no...
2.
Hendrickson P, Oristian K, Browne M, Luo L, Ma Y, Cardona D, et al.
Res Sq
. 2023 Nov;
PMID: 37961185
CIC-DUX4 sarcoma (CDS) is a rare but highly aggressive undifferentiated small round cell sarcoma driven by a fusion between the tumor suppressor Capicua (CIC) and DUX4. Currently, there are no...
3.
Hendrickson P, Oristian K, Browne M, Lou L, Ma Y, Cardona D, et al.
bioRxiv
. 2023 Oct;
PMID: 37808628
CIC-DUX4 sarcoma (CDS) is a rare but highly aggressive undifferentiated small round cell sarcoma driven by a fusion between the tumor suppressor Capicua (CIC) and DUX4. Currently, there are no...
4.
Bargiela M, Kueper J, Serebrakian A, Browne M, Brogna S, Peacock Z, et al.
J Craniofac Surg
. 2023 Mar;
34(3):849-854.
PMID: 36944600
Arhinia, or congenital absence of the nose, is an exceedingly rare anomaly caused by pathogenic variants in the gene SMCHD1 . Arhinia exhibits unique reconstructive challenges, as the midface is...
5.
Inoue K, Bostan H, Browne M, Bevis O, Bortner C, Moore S, et al.
Sci Adv
. 2023 Feb;
9(7):eabq7744.
PMID: 36800423
mutations cause congenital arhinia (absent nose) and a muscular dystrophy called FSHD2. In FSHD2, loss of SMCHD1 repressive activity causes expression of double homeobox 4 (DUX4) in muscle tissue, where...