Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

34 results
Display

Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome

Kim EN, Song DE, Yoon HM, Lee BH, Kim CJ

Patients with Beckwith-Wiedemann syndrome (BWS) are predisposed to developing embryonal tumors, with hepatoblastoma being the most common type. Our patient showed hemihypertrophy, macroglossia, and paternal uniparental disomy in chromosome 11...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Molecular cloning and characterization of porcine ribosomal protein L21

Sun WS, Chun JL, Kim DH, Ahn JS, Kim MK, Hwang IS, Kwon DJ, Hwang S, Lee JW

Ribosomal protein L21 (RPL21) is a structural component of the 60S subunit of the eukaryotic ribosome. This protein has an important role in protein synthesis and the occurrence of hereditary...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
MLL-SEPT5 Fusion Transcript in Two de novo Acute Myeloid Leukemia Patients With t(11;22)(q23;q11)

Wang N, Wu X, Sheng G, Ma L, Wen L, Yao H, Chen S

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Rare Case of Pediatric T Lymphoblastic Leukemia With t(11;17)(q23;q21) Involving Mixed-Lineage Leukemia Gene Rearrangement

Kim H, Lee JK, Lee JA, Hong YJ, Hong SI, Jo HS, Chang YH

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The First Korean Patient with Potocki-Shaffer Syndrome: A Rare Cause of Multiple Exostoses

Sohn YB, Yim SY, Cho EH, Kim OH

Potocki-Shaffer syndrome (PSS, OMIM #601224) is a rare contiguous gene deletion syndrome caused by haploinsufficiency of genes located on the 11p11.2p12. Affected individuals have a number of characteristic features including...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Constitutional Chromosomal Abnormality Identified in a Sibling Donor After Bone Marrow Stem Cell Transplantation in a Pediatric Patient with Acute Megakaryoblastic Leukemia

Seo BY, Choi HW, Kang MG, Cho D, Kee SJ, Kim SH, Shin JH, Suh SP, Ryang DW, Shin MG

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The First Korean Case of Childhood Acute Myeloid Leukemia with Inv(11)(p15q22)/NUP98-DDX10 Rearrangement: A Rare but Recurrent Genetic Abnormality

Choi R, Jang MA, Yoo KH, Lee ST, Kim HJ, Kim SH

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acute Lymphoblastic Leukemia with Mature B-Cell Phenotype and t(9;11;11)(p22;q23;p11.2): A Case Study and Literature Review

Kim B, Lee ST, Kim HJ, Lee SH, Yoo KH, Koo HH, Kim SH

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Beta-Thalassemia Minor Is Associated with IgA Nephropathy

Kang JH, Park BR, Kim KS, Kim DY, Huh HJ, Chae SL, Shin SJ

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Mantle Cell Lymphoma with Meningioma

Kim ES, Goh PG, Kim YJ, Lee SY, Moon HS, Sung JK, Lee BS, Jeong HY

Mantle cell lymphoma (MCL) is an uncommon type of gastrointestinal lymphoma. MCL is a distinct subtype of B-cell non-Hodgkin lymphomas. The major subtype of MCL is characterized by the presence...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case with Emanuel Syndrome Resulting from a Maternal Balanced Translocation

Kim JH, Kim YM, Lee BH, Kim JH, Seo EJ, Yoo HW

Emanuel syndrome is a rare genomic syndrome which is characterized by multiple congenital anomalies and developmental disability. This syndrome is related to the presence of the supernumerary derivative chromosome originating...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
CD5-negative Blastoid Variant Mantle Cell Lymphoma with Complex CCND1/IGH and MYC Aberrations

Seok Y, Kim J, Choi JR, Kim YR, Park SJ, Kim SJ, Song J, Lee KA

The coexistence of CCND1/IGH and MYC rearrangements in mantle cell lymphoma (MCL) is a rare finding associated with a very poor prognosis. In this study, a patient with blastoid variant...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Three-way Translocation of MLL/MLLT3, t(1;9;11)(p34.2;p22;q23), in a Pediatric Case of Acute Myeloid Leukemia

Jun KR, Lee JN, Park JA, Kim HR, Shin JH, Oh SH, Lee JY, Song SA

The chromosome band 11q23 is a common target region of chromosomal translocation in different types of leukemia, including infantile leukemia and therapy-related leukemia. The target gene at 11q23, MLL, is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Genome-Wide Association Scan of Korean Autism Spectrum Disorders with Language Delay: A Preliminary Study

Cho SC, Yoo HJ, Park M, Cho IH, Kim BN, Kim JW, Shin MS, Park TW, Son JW, Chung US, Kim HW, Yang YH, Kang JO, Yang SY, Kim SA

  • KMID: 2315930
  • Psychiatry Investig.
  • 2011 Mar;8(1):61-66.
OBJECTIVE: Communication problems are a prevalent symptom of autism spectrum disorders (ASDs), which have a genetic background. Although several genome-wide studies on ASD have suggested a number of candidate genes,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Therapy-related Acute Lymphoblastic Leukemia with t(11;19)(q23;p13.3) and MLL/MLLT1 Gene Rearrangement

Yoo BJ, Nam MH, Sung HJ, Lim CS, Lee CK, Cho YJ, Lee KN, Yoon SY

Therapy-related ALL (t-ALL) is a rare secondary leukemia that develops after chemotherapy and/or radiotherapy for primary malignancies. Chromosomal 11q23 abnormalities are the most common karyotypic alterations in t-ALL. The t(11;19)(q23;p13)...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Supernumerary Derivative (22) Syndrome Resulting from a Paternal Balanced Translocation

Jun YS, So CH, Yu ST, Park DS, Cho EH, Oh YK

  • KMID: 2144477
  • J Korean Soc Neonatol.
  • 2010 May;17(1):127-131.
Supernumerary derivative (22) syndrome is a rare genomic syndrome. It is characterized by severe mental retardation, microcephaly, failure to thrive, preauricular tag or sinus, ear abnormalities, cleft and/or high-arched palate,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clathrin Assembly Lymphoid Myeloid Leukemia-AF10-positive Acute Leukemias: A Report of 2 Cases with a Review of the Literature

Huh JY, Chung S, Oh D, Kang MS, Eom HS, Cho EH, Han MH, Kong SY

The translocation t(10;11)(p13;q14q21) has been found to be recurrent in acute lymphoblastic and myeloid leukemias, and results in the fusion of the clathrin assembly lymphoid myeloid leukemia (CALM) gene with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Regulation of Immune Responses by the Activating and Inhibitory Myeloid-Associate Immunoglobuline-Like Receptors (MAIR) (CD300)

Shibuya A, Nakahashi-Oda C, Tahara-Hanaoka S

Activating and inhibitory cell surface receptors play important roles in regulation of immune responses. Recent progress has demonstrated that many inhibitory receptors pair with activating, as well as inhibitory, isoforms,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Partial Trisomy 1q41 Syndrome Delineated by Whole Genomic Array Comparative Genome Hybridization

Shin YB, Nam SO, Seo EJ, Kim HH, Chang CL, Lee EY, Son HC, Hwang SH

Partial trisomy 1q syndrome is a rare chromosomal abnormality. We report on a male infant with 46,XY,der(11)t(1;11)(q41;p15.5) due to unbalanced segregation of the maternal reciprocal balanced translocation 46,XX,t(1;11)(q41;p15.5). The baby...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A De Novo Centric Fission of Chromosome 11 in a Patient with Recurrent Miscarriages

Shim SH, Lee CH, Lee JY, Shin ES, Kyhm JH, Park MI, Chung SR, Cho YH

We report on a de novo centric fission of chromosome 11 in a healthy female referred for chromosome analysis due to recurrent miscarriages. Both fission products were mitotically stable. This...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2022 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr