WordNet

small room in which a monk or nun lives (同)cubicle
a device that delivers an electric current as the result of a chemical reaction (同)electric cell
a room where a prisoner is kept (同)jail cell, prison cell
(biology) the basic structural and functional unit of all organisms; they may exist as independent units of life (as in monads) or may form colonies or tissues as in higher plants and animals
any small compartment; "the cells of a honeycomb"
a small unit serving as part of or as the nucleus of a larger political movement (同)cadre
(genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism (同)genetic mutation, chromosomal_mutation
a change or alteration in form or qualities

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1. 身体化：疫学、病因、臨床的特徴、医学的評価、および診断 somatization epidemiology pathogenesis clinical features medical evaluation and diagnosis
2. 身体化：治療および予後 somatization treatment and prognosis
3. 心気症：疫学、臨床症状、評価、および診断 hypochondriasis epidemiology clinical presentation assessment and diagnosis
4. 本態性環境不耐性（多種化学物質過敏症）の概要 overview of idiopathic environmental intolerance multiple chemical sensitivity
5. 成人における転換性障害：用語、診断および鑑別診断 conversion disorder in adults terminology diagnosis and differential diagnosis

Immune deficiency augments the prevalence of p53 loss of heterozygosity in spontaneous tumors but not bi-directional loss of heterozygosity in bone marrow progenitors.

Shetzer Y1, Napchan Y1, Kaufman T1, Molchadsky A1, Tal P1, Goldfinger N1, Rotter V1.
International journal of cancer.Int J Cancer.2017 Mar 15;140(6):1364-1369. doi: 10.1002/ijc.30554.
p53 loss of heterozygosity (LOH) is a frequent event in tumors of somatic and Li-Fraumeni syndrome patients harboring p53 mutation. Here, we focused on resolving a possible crosstalk between the immune-system and p53 LOH. Previously, we reported that p53 heterozygous bone-marrow mesenchymal progenit
PMID 28008605

Splenic diffuse red pulp lymphoma has a distinct pattern of somatic mutations amongst B-cell malignancies.

Traverse-Glehen A1,2, Verney A2, Gazzo S2,3, Jallades L2,4, Chabane K2,4, Hayette S2,4, Coiffier B2,5, Callet-Bauchu E2,3, Ffrench M4, Felman P2,4, Berger F1,2, Baseggio L2,4, Salles G2,5.
Leukemia & lymphoma.Leuk Lymphoma.2017 Mar;58(3):666-675. doi: 10.1080/10428194.2016.1196813. Epub 2016 Jun 27.
Splenic Diffuse Red Pulp Lymphoma (SDRPL) has been recently introduced as a provisional entity but differential diagnosis with other splenic lymphomas is needed to be clarified since the therapeutic approaches are distinct. Recently described recurrent mutations or CD180 expression appear useful for
PMID 27347751

Berthon A1, Faucz F1, Bertherat J2, Stratakis CA3.
Molecular and cellular endocrinology.Mol Cell Endocrinol.2017 Feb 5;441:140-145. doi: 10.1016/j.mce.2016.08.018. Epub 2016 Aug 24.
Mutations in ARMC5 gene have been recently identified as the main cause of Primary Macronodular Adrenocortical Hyperplasia (PMAH). PMAH patients have an ARMC5 germline mutation and, in addition, somatic tissue-specific mutations. This is consistent with the two-hit hypothesis of tumorigenesis and su
PMID 27568465