Ji Yoo Kim
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Explore the profile of Ji Yoo Kim including associated specialties, affiliations and a list of published articles.
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11
Citations
186
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Recent Articles
1.
Park S, Kim J, Seol K, Roh J, Lee H, Kim S, et al.
J Pediatr Surg
. 2024 Jan;
59(6):1077-1082.
PMID: 38168548
Background: Right-sided congenital diaphragmatic hernia (RCDH) is a rare and often fatal congenital anomaly, primarily attributed to lung hypoplasia, which is associated with small branch pulmonary artery (PA). This study...
2.
Jang W, Choi Y, Kim J, Yon D, Lee Y, Chung S, et al.
J Med Internet Res
. 2023 Jul;
25:e47612.
PMID: 37428525
Background: Respiratory distress syndrome (RDS) is a disease that commonly affects premature infants whose lungs are not fully developed. RDS results from a lack of surfactant in the lungs. The...
3.
Fujisaki H, Takai K, Sawada A, Tokimasa S, Matsuda Y, Ohta H, et al.
Int J Hematol
. 2018 Jan;
75(1):72-77.
PMID: 29349648
A monosomy 7 leukemia cell line, designated MONO-7, was established from the peripheral blood of a patient with monosomy 7 acute myelocytic leukemia (French-American-British classification M0). The cells were cultured...
4.
Kitaoka T, Namba N, Kim J, Kubota T, Miura K, Miyoshi Y, et al.
Clin Pediatr Endocrinol
. 2013 Aug;
18(3):81-6.
PMID: 23926365
We report a male infant with FATCO syndrome, an acronym for fibular aplasia, tibial campomelia, and oligosyndactyly. Courtens et al. reported an infant with oligosyndactyly of the left hand, complete...
5.
Sawada A, Sato E, Koyama M, Higuchi B, Kusuki S, Kim J, et al.
Am J Hematol
. 2006 Jul;
81(8):576-81.
PMID: 16823820
Epstein-Barr virus (EBV) occasionally infects T and NK cells and causes EBV-infected T/NK-cell lymphoproliferative disease (LPD), which comprises chronic active EBV infection, EBV-associated hemophagocytic syndrome, mosquito allergy, hydroa vacciniforme, aggressive...
6.
Kim J, Sawada A, Tokimasa S, Endo H, Ozono K, Hara J, et al.
Eur J Haematol
. 2004 Jul;
73(2):75-84.
PMID: 15245505
The rae28 gene (rae28) is a member of a Polycomb-group (PcG) complex 1, which is known to help maintain transcription states once these have been initiated, by generating heritable higher-order...
7.
Kubota K, Kim J, Sawada A, Tokimasa S, Fujisaki H, Matsuda-Hashii Y, et al.
FEBS Lett
. 2004 Apr;
564(1-2):147-52.
PMID: 15094057
In a previous study, we isolated a novel gene, LRRC8 (leucine-rich repeat-containing 8), in a girl with congenital agammaglobulinemia. We have now identified four unknown LRRC8-like genes, named TA-LRRP, AD158,...
8.
Sawada A, Takihara Y, Kim J, Matsuda-Hashii Y, Tokimasa S, Fujisaki H, et al.
J Clin Invest
. 2003 Dec;
112(11):1707-13.
PMID: 14660746
A girl with congenital agammaglobulinemia and minor facial anomalies lacked B cells in peripheral blood: karyotypic analysis of white blood cells showed balanced translocation, t(9;20)(q33.2;q12). In the current study, we...
9.
Koga H, Kaji Y, Nishii K, Shirai M, Tomotsune D, Osugi T, et al.
Lab Invest
. 2002 Apr;
82(4):375-85.
PMID: 11950896
The Polycomb-group genes (PcG) are widely conserved from Drosophila to mammals and are required for maintaining positional information during development. The rae28 gene (rae28) is a member of the mouse...
10.
Ohta H, Sawada A, Kim J, Tokimasa S, Nishiguchi S, Humphries R, et al.
J Exp Med
. 2002 Mar;
195(6):759-70.
PMID: 11901201
The rae28 gene (rae28), also designated as mph1, is a mammalian ortholog of the Drosophila polyhomeotic gene, a member of Polycomb group genes (PcG). rae28 constitutes PcG complex 1 for...