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  1. Article ; Online: A Case of Genetically Confirmed Pseudohypoparathyroidism Type 1a Presented with Multifocal Plate-Like Osteoma Cutis and Review of Literature.

    Kim, Jee-Woo / Kim, Minjae / Kim, Boram / Lee, Jee-Soo / Seong, Moon-Woo / Na, Jung-Im

    Annals of dermatology

    2023  Volume 35, Issue Suppl 2, Page(s) S385–S387

    Language English
    Publishing date 2023-12-05
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 1012662-4
    ISSN 2005-3894 ; 1013-9087
    ISSN (online) 2005-3894
    ISSN 1013-9087
    DOI 10.5021/ad.22.120
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 2800: Show issues Location:
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    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  2. Article ; Online: Comparison of Measurable Residual Disease in Pediatric B-Lymphoblastic Leukemia Using Multiparametric Flow Cytometry and Next-Generation Sequencing.

    Hwang, Sang Mee / Oh, Inseong / Kwon, Seok Ryun / Lee, Jee-Soo / Seong, Moon-Woo

    Annals of laboratory medicine

    2024  Volume 44, Issue 4, Page(s) 354–358

    Abstract: Measurable residual disease (MRD) testing, a standard procedure in B-lymphoblastic leukemia (B-ALL) diagnostics, is assessed using multiparametric flow cytometry (MFC) and next-generation sequencing (NGS) analysis of immunoglobulin gene rearrangements. ... ...

    Abstract Measurable residual disease (MRD) testing, a standard procedure in B-lymphoblastic leukemia (B-ALL) diagnostics, is assessed using multiparametric flow cytometry (MFC) and next-generation sequencing (NGS) analysis of immunoglobulin gene rearrangements. We evaluated the concordance between eight-color, two-tube MFC-MRD the LymphoTrack NGS-MRD assays using 139 follow-up samples from 54 pediatric patients with B-ALL. We also assessed the effect of hemodilution in MFC-MRD assays. The MRD-concordance rate was 79.9% (N=111), with 25 (18.0%) and 3 (2.2%) samples testing positive only by NGS-MRD (MFC
    MeSH term(s) Humans ; Child ; Flow Cytometry/methods ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics ; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma ; Neoplasm, Residual/diagnosis ; Neoplasm, Residual/genetics ; High-Throughput Nucleotide Sequencing/methods
    Language English
    Publishing date 2024-01-19
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2677441-0
    ISSN 2234-3814 ; 2234-3814
    ISSN (online) 2234-3814
    ISSN 2234-3814
    DOI 10.3343/alm.2023.0412
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Acral Pigmentation in Peutz-Jeghers Syndrome: Dermoscopic Findings and Treatment with the Q-Switched Nd:YAG Laser.

    Shin, Hyeonwoo / Hur, Keunyoung / Lee, Jee-Soo / Seong, Moon-Woo / Mun, Je-Ho

    Annals of dermatology

    2023  Volume 35, Issue Suppl 2, Page(s) S201–S204

    Abstract: Peutz-Jeghers syndrome (PJS; MIM 175200) is an autosomal dominant multiple-organ cancer syndrome. It is characterized by brown macules distributed in the perioral skin, oral mucosa, hands and feet, and hamartomatous gastrointestinal polyps that can ... ...

    Abstract Peutz-Jeghers syndrome (PJS; MIM 175200) is an autosomal dominant multiple-organ cancer syndrome. It is characterized by brown macules distributed in the perioral skin, oral mucosa, hands and feet, and hamartomatous gastrointestinal polyps that can eventually lead to intestinal obstruction, abdominal pain, bleeding, and anemia. Patients with PJS are at a higher risk of ovarian, testicular, breast, lung, and pancreatic cancers. This predisposition is due to the pathogenic variant in serine/threonine kinase 11 (
    Language English
    Publishing date 2023-12-05
    Publishing country Korea (South)
    Document type Case Reports
    ZDB-ID 1012662-4
    ISSN 2005-3894 ; 1013-9087
    ISSN (online) 2005-3894
    ISSN 1013-9087
    DOI 10.5021/ad.21.215
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

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    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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  4. Article ; Online: Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation.

    Lee, Heerah / Chae, Seung-Won / Cho, Sung Im / Lee, Jee-Soo / Kim, Man Jin / Seong, Moon-Woo

    International journal of molecular sciences

    2024  Volume 25, Issue 5

    Abstract: Chimerism monitoring following allogeneic hematopoietic cell transplantation (HCT) plays a pivotal role in evaluating engraftment status and identifying early indicators of relapse. Recent advancements in next-generation sequencing (NGS) technology have ... ...

    Abstract Chimerism monitoring following allogeneic hematopoietic cell transplantation (HCT) plays a pivotal role in evaluating engraftment status and identifying early indicators of relapse. Recent advancements in next-generation sequencing (NGS) technology have introduced AlloSeq HCT as a more sensitive alternative to short tandem repeat (STR) analysis. This study aimed to compare AlloSeq HCT with STR, focusing on the prediction of early relapse post-allogeneic HCT. Chimerism levels in 29 HCT recipients were assessed using both STR and NGS, employing a total of 125 whole blood or bone marrow aspirate samples (68 post-HCT and 57 pre-HCT samples from recipients or donors). AlloSeq HCT exhibited high concordance with STR and demonstrated the potential for early detection of chimeric changes, particularly at extremely low levels. The combined advantages of high sensitivity and automated data analysis offered by AlloSeq HCT substantiate its clinical adoption for effective chimerism monitoring.
    MeSH term(s) Humans ; Chimerism ; Transplantation Chimera ; Hematopoietic Stem Cell Transplantation ; Chronic Disease ; Recurrence ; High-Throughput Nucleotide Sequencing
    Language English
    Publishing date 2024-02-28
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms25052811
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A case of donor cell leukemia driven by a de novo NRAS mutation with complex karyotype.

    Jeong, Dajeong / Gu, Ja-Yoon / Seo, Myoung-Seock / Lee, Jee-Soo / Chang, Yoon Hwan / Seong, Moon-Woo / Yoon, Sung-Soo / Kim, Hyun Kyung

    Annals of hematology

    2023  Volume 102, Issue 7, Page(s) 1951–1952

    MeSH term(s) Humans ; Leukemia, Myeloid, Acute/genetics ; Mutation ; Karyotype ; Membrane Proteins/genetics ; GTP Phosphohydrolases/genetics
    Chemical Substances NRAS protein, human (EC 3.6.1.-) ; Membrane Proteins ; GTP Phosphohydrolases (EC 3.6.1.-)
    Language English
    Publishing date 2023-05-31
    Publishing country Germany
    Document type Case Reports ; Letter
    ZDB-ID 1064950-5
    ISSN 1432-0584 ; 0939-5555 ; 0945-8077
    ISSN (online) 1432-0584
    ISSN 0939-5555 ; 0945-8077
    DOI 10.1007/s00277-023-05291-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Uh III Zs.181: Show issues Location:
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  6. Article ; Online: Variant Allele Frequency of Pseudogene-Related Variants in Short-read Next-Generation Sequencing Data May Mislead Genetic Diagnosis: A Case of Shwachman-Diamond Syndrome.

    Lee, Heerah / Lee, Jung Ae / Lee, Hyesu / Lee, Jee-Soo / Ko, Jung Min / Kim, Man Jin / Seong, Moon-Woo

    Annals of laboratory medicine

    2023  Volume 43, Issue 6, Page(s) 638–641

    MeSH term(s) Humans ; Shwachman-Diamond Syndrome ; Pseudogenes ; High-Throughput Nucleotide Sequencing ; Gene Frequency
    Language English
    Publishing date 2023-06-30
    Publishing country Korea (South)
    Document type Case Reports ; Letter
    ZDB-ID 2677441-0
    ISSN 2234-3814 ; 2234-3814
    ISSN (online) 2234-3814
    ISSN 2234-3814
    DOI 10.3343/alm.2023.43.6.638
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Using Transcriptome Analysis to Explore Gray Mold Resistance-Related Genes in Onion (

    Lee, Hyun-Min / Park, Jee-Soo / Kim, So-Jeong / Kim, Seung-Gyu / Park, Young-Doo

    Genes

    2022  Volume 13, Issue 3

    Abstract: Gray mold disease caused ... ...

    Abstract Gray mold disease caused by
    MeSH term(s) Gene Expression Profiling ; Onions/genetics ; Plant Breeding ; Plant Leaves/genetics ; Random Amplified Polymorphic DNA Technique
    Language English
    Publishing date 2022-03-18
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2527218-4
    ISSN 2073-4425 ; 2073-4425
    ISSN (online) 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes13030542
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Molecular basis and diagnosis of thalassemia.

    Lee, Jee-Soo / Cho, Sung Im / Park, Sung Sup / Seong, Moon-Woo

    Blood research

    2021  Volume 56, Issue S1, Page(s) S39–S43

    Abstract: Thalassemia is characterized by the impaired synthesis of globin chains due to disease-causing variants in α- or β-globin genes. In this review, we provide an overview of the molecular basis underlying α- and β-thalassemia, and of the current ... ...

    Abstract Thalassemia is characterized by the impaired synthesis of globin chains due to disease-causing variants in α- or β-globin genes. In this review, we provide an overview of the molecular basis underlying α- and β-thalassemia, and of the current technologies used to characterize these disease-causing variants for the diagnosis of thalassemia. Understanding these molecular basis and technologies will prove to be beneficial for the accurate diagnosis of thalassemia.
    Language English
    Publishing date 2021-05-03
    Publishing country Korea (South)
    Document type Journal Article ; Review
    ZDB-ID 2711910-5
    ISSN 2288-0011 ; 2287-979X
    ISSN (online) 2288-0011
    ISSN 2287-979X
    DOI 10.5045/br.2021.2020332
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Clinical Practice Guideline for Blood-based Circulating Tumor DNA Assays.

    Lee, Jee-Soo / Cho, Eun Hye / Kim, Boram / Hong, Jinyoung / Kim, Young-Gon / Kim, Yoonjung / Jang, Ja-Hyun / Lee, Seung-Tae / Kong, Sun-Young / Lee, Woochang / Shin, Saeam / Song, Eun Young

    Annals of laboratory medicine

    2024  Volume 44, Issue 3, Page(s) 195–209

    Abstract: Circulating tumor DNA (ctDNA) has emerged as a promising tool for various clinical applications, including early diagnosis, therapeutic target identification, treatment response monitoring, prognosis evaluation, and minimal residual disease detection. ... ...

    Abstract Circulating tumor DNA (ctDNA) has emerged as a promising tool for various clinical applications, including early diagnosis, therapeutic target identification, treatment response monitoring, prognosis evaluation, and minimal residual disease detection. Consequently, ctDNA assays have been incorporated into clinical practice. In this review, we offer an in-depth exploration of the clinical implementation of ctDNA assays. Notably, we examined existing evidence related to pre-analytical procedures, analytical components in current technologies, and result interpretation and reporting processes. The primary objective of this guidelines is to provide recommendations for the clinical utilization of ctDNA assays.
    MeSH term(s) Humans ; Circulating Tumor DNA/genetics ; Biomarkers, Tumor/genetics ; Prognosis ; Neoplasm, Residual/genetics ; Mutation ; High-Throughput Nucleotide Sequencing
    Chemical Substances Circulating Tumor DNA ; Biomarkers, Tumor
    Language English
    Publishing date 2024-01-15
    Publishing country Korea (South)
    Document type Review ; Guideline
    ZDB-ID 2677441-0
    ISSN 2234-3814 ; 2234-3814
    ISSN (online) 2234-3814
    ISSN 2234-3814
    DOI 10.3343/alm.2023.0389
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Extensive Heterogeneity in the Meta-analysis of Hyperbaric Oxygen Therapy for Idiopathic Sudden Sensorineural Hearing Loss-Reply.

    Rhee, Tae-Min / Lee, Jee-Soo / Hwang, Doyeon

    JAMA otolaryngology-- head & neck surgery

    2019  Volume 145, Issue 5, Page(s) 484

    MeSH term(s) Hearing Loss, Sensorineural ; Hearing Loss, Sudden ; Humans ; Hyperbaric Oxygenation
    Language English
    Publishing date 2019-03-28
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2701825-8
    ISSN 2168-619X ; 2168-6181
    ISSN (online) 2168-619X
    ISSN 2168-6181
    DOI 10.1001/jamaoto.2019.0140
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