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Author(↓)	Class(↓)	Name(↓)	Type(↓)	Date(↓)	Affiliation(↓)
Uchimaru K	CASE_REPORT_HEMAT	An adult case of biphenotypic acute leukemia with t(6;14)(q25;q32)	CREATED	2015-09	Department of Hematology/Oncology, Research Hospital (KT, OM, TT, TR, OK, YK, FT, ON, UK, TA); Division of Cell Therapy, Advanced Clinical Research Center (TF); Division of Molecular Therapy, Advanced Clinical Research Center, The Institute of Medical Science, the University of Tokyo (TA), 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan. Toyotaka Kawamata: toyotaka@ims.u-tokyo.ac.jp, Miho Ogawa: miho.ogawa327@gmail.com; Tomomi Takei: t-takei@ims.u-tokyo.ac.jp; Reina Takeda: reina.takeda@gmail.com; Kiyosumi Ochi: equuleus2015@gmail.com; Kazuaki Yokoyama: k-yoko@ims.u-tokyo.ac.jp; Tomofusa Fukuyama: tfukuyam@ims.u-tokyo.ac.jp; Nobuhiro Ohno: nobuohno@ims.u-tokyo.ac.jp; Kaoru Uchimaru: uchimaru@ims.u-tokyo.ac.jp; Arinobu Tojo: a-tojo@ims.u-tokyo.ac.jp
Ueno NT	GENE	PEA15 (phosphoprotein enriched in astrocytes 15)	CREATED	2012-05	Section of Translational Breast Cancer Research, Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA
Uhlmann S	GENE	MIR200C (microRNA 200c)	CREATED	2011-08	Division of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Division of Molecular Genome Analysis, Im Neuenheimer Feld 580, Heidelberg, Germany
Uhrhammer N	DEEP_INSIGHT	Ataxia-Telangiectasia and variants	CREATED	2002-04	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	GENE	ATM (ataxia telangiectasia mutated)	UPDATED	1999-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	GENE	ATM (ataxia telangiectasia mutated)	UPDATED	2002-11	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	GENE	CHEK2 (CHK2 checkpoint homolog (S. pombe))	CREATED	2004-05	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	GENE	MRE11 meiotic recombination 11 homolog A (S. cerevisiae)	CREATED	2004-05	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	GENE	NBN (Nijmegen breakage syndrome 1)	UPDATED	1999-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	GENE	NBN (Nijmegen breakage syndrome 1)	UPDATED	2002-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	K_PRONE	Ataxia telangiectasia (A-T)	UPDATED	1999-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	K_PRONE	Ataxia telangiectasia (A-T)	UPDATED	2002-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	K_PRONE	Nijmegen breakage syndrome	UPDATED	1999-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Uhrhammer N	K_PRONE	Nijmegen breakage syndrome	UPDATED	2002-10	Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France
Underdown MJ	CHROM_CLIN	dic(7;9)(p11-13;p11)	UPDATED	2019-04	Department of Pediatrics, Wake Forest School of Medicine, Winston Salem, North Carolina (MJU); Section of Pediatric Hematology-Oncology, Department of Pediatrics, Wake Forest School of Medicine, Winston Salem, North Carolina (DEK, TBR); Department of Pathology, Wake Forest School of Medicine, Winston Salem, USA (MJP), Medical Center Boulevard, Winston Salem, NC, USA 27157; dkram@wakehealth.edu
Urbé S	GENE	USP15 (ubiquitin specific peptidase 15)	CREATED	2010-12	Physiology Department, School of Biomedical Sciences, Faculty of Health, Life Sciences, University of Liverpool, Crown Street, Liverpool, L69 3BX, UK
Urfali-Mamatoglu C	GENE	PDCD10 (Programmed cell death 10)	CREATED	2016-08	Department of Biological Sciences, Middle East Technical University, Ankara, Turkey. cagri.urfali@metu.edu.tr; hasanhuseyinkazan@gmail.com; ufukg@metu.edu.tr
User SD	GENE	GADD45A (growth arrest and DNA-damage-inducible, alpha)	CREATED	2014-06	Department of Biological Sciences, Middle East Technical University, Ankara, Turkey
Uva V	DEEP_INSIGHT	FOXP3 expression in tumor cells and its role in cancer progression	CREATED	2014-10	Molecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy (VU, TT, PC, ET); Dipartimento di Scienze Biomediche per la Salute, Universita degli Studi di Milano, Milan, Italy (LS, AB)
Uzunova V	CASE_REPORT_HEMAT	Isolated 1q21 rearrangement der(20)t(1;20)(q21;p13) with telomere involvement of 20p in a case of longstanding myelodysplastic syndrome	CREATED	2017-06	Department of Cytogenetics and Molecular Biology (LM, LG, AA, VU), Clinical of Haematology (JR), Military Medical Academy, Sofia, Bulgaria, cytogen.vma@abv.bg