WordNet

arrange into a group or groups; "Can you group these shapes together?"
(chemistry) two or more atoms bound together as a single unit and forming part of a molecule (同)radical, chemical group
any number of entities (members) considered as a unit (同)grouping
a set that is closed, associative, has an identity element and every element has an inverse (同)mathematical group
form a group or group together (同)aggroup
the activity of putting things together in groups
a system for classifying things into groups (同)pigeonholing
any of a large group of nitrogenous organic compounds that are essential constituents of living cells; consist of polymers of amino acids; essential in the diet of animals for growth and for repair of tissues; can be obtained from meat and eggs and milk and legumes; "a diet high in protein"
a unit of force equal to the force exerted by gravity; used to indicate the force to which a body is subjected when it is accelerated (同)gee, g-force
a deficiency of red blood cells (同)anaemia
a lack of vitality (同)anaemia

PrepTutorEJDIC

(…の)『群れ』,集まり,小集団《+of+名》 / (主義・系統・種類などを同じくする人・物の)『派』,『団体』 / (ポミュラーソング歌手の)グループ / (動・植物分類上の)群;(化学の)基,原子団;(地質学上の)界;(数学の)群;(言語学上の)語派 / …‘を'一群に集める,一団にする《+『名』+『together』》 / (系統的に)…‘を'分類する,調和よく配合する《+『名』+『together』》 / 集まる,群(集団)をなす
グループに分けること;分類法 / (集まった物の)配置,配合
蛋白(たんばく)質

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1. 補体系の制御因子および受容体 regulators and receptors of the complement system
2. 小児および思春期における特発性の重症再生不良性貧血およびファンコニ貧血に対する造血細胞移植 hematopoietic cell transplantation for idiopathic severe aplastic anemia and fanconi anemia in children and adolescents
3. 補体経路 complement pathways
4. ペプチドホルモンのシグナル伝達および調節 peptide hormone signal transduction and regulation
5. 補体系の後天性疾患 acquired disorders of the complement system

A case report of Fanconi anemia diagnosed by genetic testing followed by prenatal diagnosis.

Lee HJ, Park S, Kang HJ, Jun JK, Lee JA, Lee DS, Park SS, Seong MW.SourceDepartment of Laboratory Medicine, Seoul National University Hospital, Seoul, Korea.
Annals of laboratory medicine.Ann Lab Med.2012 Sep;32(5):380-4. doi: 10.3343/alm.2012.32.5.380. Epub 2012 Aug 13.
Fanconi anemia (FA) is a rare genetic disorder affecting multiple body systems. Genetic testing, including prenatal testing, is a prerequisite for the diagnosis of many clinical conditions. However, genetic testing is complicated for FA because there are often many genes that are associated with its
PMID 22950077

Barroca V, Mouthon MA, Lewandowski D, Brunet de la Grange P, Gauthier LR, Pflumio F, Boussin FD, Arwert F, Riou L, Allemand I, Romeo PH, Fouchet P.SourceLaboratoire de Gamétogenèse Apoptose et Génotoxicite, Institut de Radiobiologie Cellulaire et Moléculaire, Direction des Sciences du Vivant, Commissariat à l'Energie Atomique et aux Energies Alternatives, Fontenay-aux-Roses 92265, France.
Human molecular genetics.Hum Mol Genet.2012 Jan 1;21(1):121-35. doi: 10.1093/hmg/ddr447. Epub 2011 Oct 3.
Fanconi anemia (FA) is a human rare genetic disorder characterized by congenital defects, bone marrow (BM) failure and predisposition to leukemia. The progressive aplastic anemia suggests a defect in the ability of hematopoietic stem cells (HSC) to sustain hematopoieis. We have examined the role of
PMID 21968513

Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg.

van de Vrugt HJ, Koomen M, Bakker S, Berns MA, Cheng NC, van der Valk MA, de Vries Y, Rooimans MA, Oostra AB, Hoatlin ME, Te Riele H, Joenje H, Arwert F.SourceDepartment of Clinical Genetics, VU University Medical Center, Van der Boechorststraat 7, 1081 BT, Amsterdam, The Netherlands. henrivandevrugt@gmail.com
DNA repair.DNA Repair (Amst).2011 Dec 10;10(12):1252-61. doi: 10.1016/j.dnarep.2011.09.015. Epub 2011 Oct 28.
Fanconi anemia (FA) is a heritable disease characterized by bone marrow failure, congenital abnormalities, and cancer predisposition. The 15 identified FA genes operate in a molecular pathway to preserve genomic integrity. Within this pathway the FA core complex operates as an ubiquitin ligase that
PMID 22036606