Publications by authors named "Xianglan Lu"

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Transplantation of bone marrow cells from miR150 knockout mice improves senescence-associated humoral immune dysfunction and arterial stiffness.
Jun Fan, Shirley Wang, Xianglan Lu, Zhongjie Sun

Metabolism· September 2022

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Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies.
Austin Walker, Xianfu Wang, Young Mi Kim, Xianglan Lu, Ashley Taylor

Mol Cytogenet· April 2022

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Methylation of SPRED1: A New Target in Acute Myeloid Leukemia.
Nan Su, Yujiao Wang, Xianglan Lu, Weihong Xu, He Wang

Front Oncol· March 2022

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Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation.
Ke Zhang, Xianglan Lu, Xuxin Chen, Roy Zhang, Kar-Ming Fung

J Biomed Opt· January 2022

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Amplification as Double Minute Chromosomes in a Patient with Chronic Myelomonocytic Leukemia.
Heyang Zhang, Xiaoxue Wang, Shibo Li, Xianfu Wang, Xianglan Lu

Dis Markers· December 2021

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Genomic Copy Number Variants in CML Patients With the Philadelphia Chromosome (Ph+): An Update.
Heyang Zhang, Meng Liu, Xiaoxue Wang, Yuan Ren, Young Mi Kim, Xianglan Lu

Front Genet· August 2021

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Difference of genomic copy numbers alterations between hairy cell leukemia-variant and classical hairy cell leukemia: a pilot retrospective study in Chinese.
Rui Zhang, Yongli Wu, Xianfu Wang, Xianglan Lu, Yan Li

Int J Med Sci· January 2021

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Identification of a cryptic submicroscopic deletion using a combination of fluorescence in situ hybridization and array comparative genomic hybridization in a t(3;5)(q25;q35)-positive acute myeloid leukemia patient: A case report and review of the literature.
Man Gao, Shibo Li, Lina Wang, Shu Nie, Hui Pang, Xianglan Lu

Medicine (Baltimore)· October 2020

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Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review.
Meng Liu, Yuan Ren, Xianfu Wang, Xianglan Lu, Ming Li

Mol Cytogenet· August 2020

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Infantile Epithelioid Sarcoma with Genomic Segmental Amplification of as Double Minutes Plus Trisomy 2: A Case Report.
Anand Srinivasan, Meng Liu, David Parham, Ming Li, Xianfu Wang, Xianglan Lu

Fetal Pediatr Pathol· February 2020

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Is Downregulated and a Prognostic Biomarker in Adult Acute Myeloid Leukemia.
Rui Zhang, Yan Zhang, Xianglan Lu, Weihong Xu, He Wang

Front Oncol· February 2020

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An extra chromosome 9 derived from either a normal chromosome 9 or a derivative chromosome 9 in a patient with acute myeloid leukemia positive for t(9;11)(p21.3;q23.3): A case report.
Man Gao, Hui Pang, Young Mi Kim, Xianglan Lu, Xianfu Wang

Oncol Lett· December 2019

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Cytogenetic characterization of the malignant primitive neuroectodermal SK-PN-DW tumor cell line.
Na Du, Wanguo Bao, Kaiyu Zhang, Xianglan Lu, Rebecca Crew

BMC Cancer· May 2019

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Simultaneous involvement of 11q23 translocation resulting in chimeric MLL-AFF1 and a second translocation [t (9;21) (p13; p11.2)] in an infant acute lymphoblastic leukemia patient at relapse: A case report.
Guangming Liu, Xianglan Lu, Young Mi Kim, Xianfu Wang, Shibo Li

Medicine (Baltimore)· May 2018

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Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29].
Valerie M Harris, Rohan Sharma, Joshua Cavett, Biji T Kurien, Ke Liu, Xianglan Lu

Clin Immunol· February 2018

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Coexistence of t(2;14;11)(p16.1;q32;q23) and t(14;19)(q32;q13.3) chromosome translocations in a patient with chronic lymphocytic leukemia: A case report.
Guangming Liu, Zhongmei Wen, Xianglan Lu, Young Mi Kim, Xianfu Wang

Medicine (Baltimore)· December 2017

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Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome.
Rohan Sharma, Valerie M Harris, Joshua Cavett, Biji T Kurien, Ke Liu, Xianglan Lu

Arthritis Rheumatol· November 2017

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Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization.
Mingran Sun, Han Zhang, Guiying Li, Carrie J Guy, Xianfu Wang, Xianglan Lu

Sci Rep· September 2017

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Clinical report: variable phenotypic expression in a large sibling cohort with a deletion of 4p16.1.
Carrie Guy, Xianfu Wang, Xianglan Lu, Jin Lu, Shibo Li

Clin Case Rep· October 2016

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A cryptic submicroscopic deletion of 5' MLF1-3' NPM1 segment on derivative chromosome 3 in a patient with acute myeloid leukemia with t(3;5)(q25;q35).
Man Gao, Guanjun Wang, Xianfu Wang, Young Mi Kim, Xianglan Lu, Jin Lu

Leuk Lymphoma· August 2016

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Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome.
Valerie M Harris, Rohan Sharma, Joshua Cavett, Biji T Kurien, Ke Liu, Xianglan Lu

Clin Immunol· July 2016

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Genomic Copy Number Variations in the Myelodysplastic Syndrome and Acute Myeloid Leukemia Patients with del(5q) and/or -7/del(7q).
Rui Zhang, Young-Mi Kim, Xianfu Wang, Yan Li, Xianglan Lu

Int J Med Sci· June 2016

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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome.
Ke Liu, Biji T Kurien, Sarah L Zimmerman, Kenneth M Kaufman, Diana H Taft, Xianglan Lu

Arthritis Rheumatol· May 2016

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Two patients with small chromosome 22q11.21 alterations and central nervous system abnormalities.
Carrie Guy, Xianfu Wang, Xianglan Lu, Jin Lu, Shibo Li

Mol Cytogenet· December 2015

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16p13.3 duplication associated with non-syndromic pierre robin sequence with incomplete penetrance.
Mingran Sun, Han Zhang, Guiying Li, Xianfu Wang, Xianglan Lu

Mol Cytogenet· December 2014

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