نتایج جستجو برای: hoxa10 gene

تعداد نتایج: 1141515  

Journal: :genetics in the 3rd millennium 0
seyed mehdi kalantar vida mokhtari

homeobox (hox) genes are contributed in the genetic control of development of the body plan, pattern formation, and cell fate determination and the other several key developmental processes. hox genes are also known as selector genes because expression within a given section of the embryo will cause its cells to choose a particular developmental path. hox genes encode transcription factors that...

Journal: :Blood 2011
Sheryl M Gough Christopher I Slape Peter D Aplan

Structural chromosomal rearrangements of the Nucleoporin 98 gene (NUP98), primarily balanced translocations and inversions, are associated with a wide array of hematopoietic malignancies. NUP98 is known to be fused to at least 28 different partner genes in patients with hematopoietic malignancies, including acute myeloid leukemia, chronic myeloid leukemia in blast crisis, myelodysplastic syndro...

Journal: :American journal of physiology. Endocrinology and metabolism 2006
Rebecca L Kelley Karen L Kind Michelle Lane Rebecca L Robker Jeremy G Thompson Lisa J Edwards

Gonadotropins are routinely administered to produce multiple oocytes for clinical in vitro fertilization (IVF) treatment, laboratory research, and livestock industries. Studies in mice have shown gonadotropin stimulation using equine chorionic gonadotropin (eCG) affects the endometrium, implantation, and fetal development. Evidence from clinical studies also indicates that stimulation with reco...

2015
Wenqing Ma Ya Li Man Wang Haixia Li Tiefen Su Yan Li Shixuan Wang Reiner Albert Veitia

BACKGROUND Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare syndrome that is characterized by congenital aplasia of the uterus and the upper portion (2/3) of the vagina. Previous attempts to identify causal mutations of MRKH syndrome have primarily resulted in negative outcomes. We investigated whether these reported variants are associated with MRKH syndrome (types I and II) in a relat...

2014
Dimitris Karamitros Alexandra L. Patmanidi Panoraia Kotantaki Alexandre J. Potocnik Tomi Bähr-Ivacevic Vladimir Benes Zoi Lygerou Dimitris Kioussis Stavros Taraviras

Balancing stem cell self-renewal and initiation of lineage specification programs is essential for the development and homeostasis of the hematopoietic system. We have specifically ablated geminin in the developing murine hematopoietic system and observed profound defects in the generation of mature blood cells, leading to embryonic lethality. Hematopoietic stem cells (HSCs) accumulated in the ...

Journal: :Blood 2013
Eva A Coenen C Michel Zwaan Dirk Reinhardt Christine J Harrison Oskar A Haas Valerie de Haas Vladimir Mihál Barbara De Moerloose Marta Jeison Jeffrey E Rubnitz Daisuke Tomizawa Donna Johnston Todd A Alonzo Henrik Hasle Anne Auvrignon Michael Dworzak Andrea Pession Vincent H J van der Velden John Swansbury Kit-fai Wong Kiminori Terui Sureyya Savasan Mark Winstanley Goda Vaitkeviciene Martin Zimmermann Rob Pieters Marry M van den Heuvel-Eibrink

In pediatric acute myeloid leukemia (AML), cytogenetic abnormalities are strong indicators of prognosis. Some recurrent cytogenetic abnormalities, such as t(8;16)(p11;p13), are so rare that collaborative studies are required to define their prognostic impact. We collected the clinical characteristics, morphology, and immunophenotypes of 62 pediatric AML patients with t(8;16)(p11;p13) from 18 co...

2016
Mona Elsafadi Muthurangan Manikandan Muhammad Atteya Jamil Amjad Hashmi Zafar Iqbal Abdullah Aldahmash Musaad Alfayez Moustapha Kassem Amer Mahmood

Human bone marrow-derived stromal stem cells (hBMSC) exhibit multiple functions, including differentiation into skeletal cells (progenitor function), hematopoiesis support, and immune regulation (nonprogenitor function). We have previously demonstrated the presence of morphological and functional heterogeneity of hBMSC cultures. In the present study, we characterized in detail two hTERT-BMSC cl...

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