검색어 : 통합검색[Human molecular genetics 3]
총 3,413건 중 1,000건 출력
, 8/100 페이지
-
71
-
Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia
-
Lahortiga, Idoya;
De Keersmaecker, Kim;
Van Vlierberghe, Pieter;
Graux, Carlos;
Cauwelier, Barbara;
Lambert, Frederic;
Mentens, Nicole;
Beverloo, H Berna;
Pieters, Rob;
Speleman, Frank;
Odero, Maria D;
Bauters, Marijke;
Froyen, Guy;
Marynen, Peter;
Vandenberghe, Peter;
Wlodarska, Iwona;
Meijerink, Jules P P;
Cools, Jan;
[1] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. [2] Human Genome Laboratory, Center for Human Genetics, Katholieke Universiteit (K.U.) Leuven, Leuven, Belgium. [3] Division of Oncology, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.;
[1] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. [2] Human Genome Laboratory, Center for Human Genetics, Katholieke Universiteit (K.U.) Leuven, Leuven, Belgium.;
Department of Pediatric Oncology/Hematology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.;
[1] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. [2] Human Genome Laboratory, Center for Human Genetics, Katholieke Universiteit (K.U.) Leuven, Leuven, Belgium. [3] D;
(Nature genetics,
v.39,
2007,
pp.593-595)
-
72
-
AQP0 is a novel surface marker for deciphering abnormal erythropoiesis
-
Wang, Tso-Fu;
Lin, Guan-Ling;
Chu, Sung-Chao;
Chen, Chang-Chin;
Liou, Yu-Shan;
Chang, Hsin-Hou;
Sun, Der-Shan;
Departments of Hematology and Oncology, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China;
Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China;
Departments of Hematology and Oncology, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China;
Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China;
Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China;
Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004 Taiwan, Republic of China;
Department of Molecular Biology and Human Genetics, Tzu-Chi University, No. 701, Section 3, Zhong-Yang Road, Hua;
(Stem cell research & therapy,
v.12,
2021,
pp.274)
-
73
-
<i>ST3GAL3</i> Mutations Impair the Development of Higher Cognitive Functions
-
Hu, Hao;
Eggers, Katinka;
Chen, Wei;
Garshasbi, Masoud;
Motazacker, M.
Mahdi;
Wrogemann, Klaus;
Kahrizi, Kimia;
Tzschach, Andreas;
Hosseini, Masoumeh;
Bahman, Ideh;
Hucho, Tim;
Mü
hlenhoff, Martina;
Gerardy-Schahn, Rita;
Najmabadi, Hossein;
Ropers, H.
Hilger;
Kuss, Andreas
W.;
Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Institute for Cellular Chemistry, Hannover Medical School, 30625 Hannover, Germany;
Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Department of Biochemistry & Medical Genetics, University of Manitoba, Winnipeg R3E OJ9, Canada;
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran 1985713834, Iran;
Department for Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran 1985713834, Iran;
Genetics Research Center, University of Social;
(American journal of human genetics,
v.89,
2011,
pp.407-414)
-
74
-
Undiagnosed disease program in South Africa: Results from first 100 exomes
-
Moosa, Shahida;
Coetzer, Kimberly Christine;
Lee, Eugene;
Seo, Go Hun;
Division of Molecular Biology and Human Genetics, Stellenbosch University, Cape Town, South Africa;
Division of Molecular Biology and Human Genetics, Stellenbosch University, Cape Town, South Africa;
3billion Inc., Seoul, Republic of Korea;
3billion Inc., Seoul, Republic of Korea;
(American Journal of Medical Genetics. Part A,
v.188,
2022,
pp.2684-2692)
-
75
-
Ulnar–mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene
-
Klopocki, Eva;
Neumann, Luitgard M;
Tö
nnies, Holger;
Ropers, Hans-Hilger;
Mundlos, Stefan;
Ullmann, Reinhard;
1Institute of Medical Genetics, Charité
Universitä
tsmedizin Berlin, Berlin, Germany;
2Institute of Human Genetics, Charité
Universitä
tsmedizin Berlin, Berlin, Germany;
2Institute of Human Genetics, Charité
Universitä
tsmedizin Berlin, Berlin, Germany;
3Max-Planck Institute for Molecular Genetics, Berlin, Germany;
1Institute of Medical Genetics, Charité
Universitä
tsmedizin Berlin, Berlin, Germany;
3Max-Planck Institute for Molecular Genetics, Berlin, Germany;
(European journal of human genetics : EJHG,
v.14,
2006,
pp.1274-1279)
-
76
-
Physical and Genetic Linkage of Glutaminase (<i>Gls</i>), Signal Transducer and Activator of Transcription 1 (<i>Stat1</i>), and Xeroderma Pigmentosum Complementation Group G (<i>Xpg</i>) on Mouse Proximal Chromosome 1
-
Lé
vy, Nicolas;
Boettger-Tong, Holly;
Dohmae, Kayoko;
Agoulnik, Alexander I.;
Ty, Theresa I.;
Nishimune, Yoshitake;
Bishop, Colin E.;
Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030;
Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030;
Research Institute for Microbial Diseases, Osaka University, Yamadaoka 3-1, Suita, Osaka, 565, Japan;
Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030;
Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030;
Research Institute for Microbial Diseases, Osaka University, Yamadaoka 3-1, Suita, Osaka, 565, Japan;
Department of Obstetrics and Gynecology, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030;
(Genomics,
v.54,
1998,
pp.355-356)
-
77
-
<i>Fgfr1</i> and <i>Fgfr2</i> have distinct differentiation- and proliferation-related roles in the developing mouse skull vault
-
Iseki, S.;
Wilkie, A. O. M.;
Morriss-Kay, G. M.;
1 Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QX, UK;
3 Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK;
1 Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QX, UK;
(Development,
v.126,
1999,
pp.5611-5620)
-
78
-
Mechanisms of change in gene copy number
-
Hastings, P. J.;
Lupski, James R.;
Rosenberg, Susan M.;
Ira, Grzegorz;
Department of Molecular and Human Genetics, Houston, Texas 77030, USA.;
[1] Department of Molecular and Human Genetics, Houston, Texas 77030, USA. [2] Department of Pediatrics, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA. [3] Texas Children's Hospital, 1102 Bates, Houston, Texas 77030, USA.;
[1] Department of Molecular and Human Genetics, Houston, Texas 77030, USA. [2] Department of Biochemistry and Molecular Biology, Houston, Texas 77030, USA. [3] Department of Molecular Virology and Microbiology, Houston, Texas 77030, USA. [4] The Dan L. Duncan Cancer Center, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.;
Department of Molecular and Human Genetics, Houston, Texas 77030, USA.;
(Nature reviews. Genetics,
v.10,
2009,
pp.551-564)
-
79
-
Delayed male germ cell sex-specification permits transition into embryonal carcinoma cells with features of primed pluripotency
-
Dawson, Emily P.;
Lanza, Denise G.;
Webster, Nicholas J.;
Benton, Susan M.;
Suetake, Isao;
Heaney, Jason D.;
Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA;
Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA;
Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA;
Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA;
Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871, Japan;
Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA;
(Development,
v.145,
2018,
pp.dev156612-dev156612)
-
80
-
Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia
-
Hoffmann, Sandra;
Berger, Ina M.;
Glaser, Anne;
Bacon, Claire;
Li, Li;
Gretz, Norbert;
Steinbeisser, Herbert;
Rottbauer, Wolfgang;
Just, Steffen;
Rappold, Gudrun;
Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany;
Department of Internal Medicine II, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany;
Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany;
Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany;
Medical Research Center, University Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany;
Medical Research Center, University Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany;
Division of Developmental Genetics, Institute of Human Genetics, University Heidelberg, INF 366, 69120 Heidelberg, Germany;
Department of Internal Medicine II, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany;
Department of Internal Medicine II, University of Ulm, Albert-Einstein-Allee 23, 89081;
(Basic research in cardiology,
v.108,
2013,
pp.339)