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Clinical and molecular genetic characterization of wild-type MLL infant acute lymphoblastic leukemia identifies few recurrent abnormalities. [electronic resource] by
- van der Linden, Marieke H
- Boer, Judith M
- Schneider, Pauline
- Willekes, Merel
- Seslija, Lidija
- De Lorenzo, Paola
- Valsecchi, Maria Grazia
- Cazzaniga, Giovanni
- Biondi, Andrea
- den Boer, Monique L
- Pieters, Rob
- Stam, Ronald W
Producer: 20170103
In:
Haematologica vol. 101
Availability: No items available.
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Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype. [electronic resource] by
- Ferretti, Elisabetta
- Villaescusa, J Carlos
- Di Rosa, Patrizia
- Fernandez-Diaz, Luis C
- Longobardi, Elena
- Mazzieri, Roberta
- Miccio, Annarita
- Micali, Nicola
- Selleri, Licia
- Ferrari, Giuliana
- Blasi, Francesco
Producer: 20060919
In:
Molecular and cellular biology vol. 26
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MEIS1, PREP1, and PBX4 are differentially expressed in acute lymphoblastic leukemia: association of MEIS1 expression with higher proliferation and chemotherapy resistance. [electronic resource] by
- Rosales-Aviña, Judith A
- Torres-Flores, Jorge
- Aguilar-Lemarroy, Adriana
- Gurrola-Díaz, Carmen
- Hernández-Flores, Georgina
- Ortiz-Lazareno, Pablo C
- Lerma-Díaz, José M
- de Celis, Ruth
- González-Ramella, Óscar
- Barrera-Chaires, Esperanza
- Bravo-Cuellar, Alejandro
- Jave-Suárez, Luis F
Producer: 20120815
In:
Journal of experimental & clinical cancer research : CR vol. 30
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Genetic markers of Restless Legs Syndrome in Parkinson disease. [electronic resource] by
- Gan-Or, Ziv
- Alcalay, Roy N
- Bar-Shira, Anat
- Leblond, Claire S
- Postuma, Ronald B
- Ben-Shachar, Shay
- Waters, Cheryl
- Johnson, Amelie
- Levy, Oren
- Mirelman, Anat
- Gana-Weisz, Mali
- Dupré, Nicolas
- Montplaisir, Jacques
- Giladi, Nir
- Fahn, Stanley
- Xiong, Lan
- Dion, Patrick A
- Orr-Urtreger, Avi
- Rouleau, Guy A
Producer: 20160502
In:
Parkinsonism & related disorders vol. 21
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