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return kwic search for genes out of >500 occurrences
299409 occurrences (No.76 in the rank) during 5 years in the PubMed. [no cache] 500 found

376) Recurrent mutations in more than 10 different genes have now been identified, involving biological pathways converging on intracellular vesicle trafficking and cytolytic granule exocytosis.

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PMID:24407034 DOI:10.1177/0885066613517076

2015 Journal of intensive care medicine

* Hemophagocytic Syndrome and Critical Illness: New Insights into Diagnosis and Management.

- Hemophagocytic lymphohistiocytosis (HLH) comprises a heterogeneous group of diseases that are characterized by a hyperinflammatory state due to uncontrolled T cell, macrophage, and histiocyte activation, accompanied by excessive cytokine production. This rare condition is almost uniformly fatal unless promptly recognized and treated. Much progress has been made in the last two decades in our understanding of the mechanisms underlying familial, and to a lesser extent, acquired cases of HLH. Recurrent mutations in more than 10 different genes have now been identified, involving biological pathways converging on intracellular vesicle trafficking and cytolytic granule exocytosis. Mechanisms underlying the majority of patients with acquired HLH, however, remain elusive, hampering both diagnostic evaluation and therapeutic management of these patients. Given that the majority of intensive care unit (ICU) patients with sepsis or multiorgan failure share many features of HLH, it is especially critical for pediatric and adult intensivists to be able to recognize patients with bona fide HLH and initiate treatment without delay. In this article, we review our current understanding of the pathophysiology, clinical testing, diagnosis, and treatment of patients with HLH, especially as it pertains to the care of critically ill patients in pediatric and medical ICUs.

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(1)101 and	(12)8 including	(23)4 for	(34)2 13
(2)36 null	(13)7 encoding	(24)4 from	(35)2 but
(3)28 are	(14)7 involved	(25)4 related	(36)2 can
(4)26 were	(15)7 which	(26)4 with	(37)2 coding
(5)25 in	(16)6 (PCGs),	(27)3 had	(38)2 expressed
(6)16 2	(17)6 use	(28)3 have	(39)2 is
(7)14 (13	(18)5 may	(29)3 stop	(40)2 on
(8)14 22	(19)5 that	(30)3 such	(41)2 ranged
(9)12 start	(20)4 (PCGs)	(31)2 (cytb,	(42)2 to
(10)11 of	(21)4 as	(32)2 (pnad1
(11)9 was	(22)4 associated	(33)2 (srfAA,

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--- WordNet output for genes --- =>発生, 起源, 起こり, 生成, 創始, 創世記 Overview of noun gene The noun gene has 1 sense (no senses from tagged texts) 1. gene, cistron, factor -- ((genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors") --- WordNet end ---