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1,250 Possible Causes for 11, HOMEOBOX

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  • Chenodeoxycholic Acid

    Improvement of evoked potentials, especially of MEPs and SEPs, was slower and continued over the whole 11-year period.[] Microarray analysis identified Hex (Hematopoietically expressed homeobox), a central transcription factor in vertebrate embryogenesis and liver development, as a novel CDCA[] Recent evidence suggested that this MR activation is, at least in part, a result of bile acid-dependent reduction in 11 beta-hydroxysteroid dehydrogenase type 2 (11 beta HSD2[]

  • Endometrioma

    OBJECTIVE: To determine whether laparoscopic endometrioma resection alters peri-implantation endometrial HOXA-10, HOXA-11, LIF, ITGB3 and ITGAV mRNA expression.[] There were 3 of them with P value 5 10 -06 , separately locating in intron of insulin-like growth factor 1 receptor, chromosome 7 open reading frame 50, and Meis homeobox[] CASE: An 11-year-old adolescent underwent an emergency operation for left ovarian endometrioma. Her menarche occurred spontaneously 6 months after surgery.[]

  • Ambiguous Genitalia

    Abstract We describe a patient with ambiguous genitalia, gonadoblastoma, aniridia, mental retardation and 46XY, del (11)(p13) karyotype.[] A novel mutation in the aristaless-related homeobox (ARX) gene causing a hemizygous nucleotide substitution in exon 5 was identified (NM_139058.2 (ARX): c.1614G T; p.K538N[] Abstract An 11-year-old girl was followed up since birth because of hemihypertrophy of the left leg and thigh, multiple pigmented nevi and subcutaneous tumors typical of the[]

  • T-cell Acute Lymphoblastic Leukemia

    Cancer Discov. 2017 Nov;7(11):1336-1353. doi: 10.1158/2159-8290.CD-17-0267. Epub 2017 Oct 3.[] […] a case of T-cell ALL in a 13-year-old boy with t(2;12)(q31;p13) involving ETV6, resulting in the relocation of the ETV6 from 12p13 to 2q31 locus that harbors the class 1 homeobox[] RUNX1 has been proposed to have tumor suppressor roles in T-cell leukemia homeobox 1/3-transformed human T-ALL cell lines and NOTCH1 T-ALL mouse models.[]

  • Trigonocephaly

    Abstract A seventh case of deletion of the distal long arm of a chromosome 11 is described.[] Abstract This communication brings the number of recognized cases of the C (trigonocephaly) syndrome to 11.[] Mean age at the time of surgery was 11 months. Mean follow-up was 9.0 years. During this time, 2 patients exhibited relapse requiring camouflage procedures.[]

  • Waardenburg Syndrome

    Among these implantees, 11 were diagnosed with WS (0.59% of all implantees).[] KEYWORDS: PAX3; arginine methylation; chromosomes; homeobox; homeodomain; mitosis; mitotic chromosome; mutant; protein arginine N-methyltransferase 5 (PRMT5); transcription[] Issa S 1, 2, 3 , Bondurand N 1, 2, 3 , Faubert E 4 , Poisson S 5 , Lecerf L 1, 2 , Nitschke P 6 , Deggouj N 7 , Loundon N 8 , Jonard L 5, 9 , David A 10 , Sznajer Y 11 , Blanchet[]

  • Becker Muscular Dystrophy

    Each of five patients had deletions of exons 11-27 in common.[] Whereas in the short brother (-2.2 SDS) molecular investigation revealed a G367A mutation in the short stature homeobox containing (SHOX) gene located in the Xp22.3 region[] He harboured a novel c.1150-3C G substitution in the DMD gene, affecting the intron 10 acceptor splice site and causing exon 11 skipping and an out-of-frame transcript.[]

  • Distal Renal Tubular Acidosis

    Two patients (16.7%) showed homozygote deletions in exon 11 of AE1 gene, and 1 patient (8.3%) showed point mutation in exon 11.[] ATP6V1B1 lies adjacent to the gene encoding the homeobox domain protein VAX2, at 2p13.3. To date, no human phenotype has been associated with VAX2 mutations.[] The clinical features of the 11 patients were also investigated.[]

  • Gastric Cancer

    Proline-rich protein 11 (PRR11) has been shown to be up-regulated in human cancers; however, its role in gastric CSCs is unknown.[] In addition, the data revealed that Neo1 positively regulated the expression of Zinc finger E-box-binding homeobox 1 (ZEB1) by activating the Rac1/PI3K/AKT pathway.[] After chemotherapy, PM disappearance was confirmed in 11 patients. Gastrectomy was eventually performed in 11 patients.[]

  • Deafness

    We present the case of an 11-year-old deaf girl with a paternal uniparental diploidy or isodisomy with a genome-wide loss of heterozygosity (LOH).[] This interval encompasses several genes, especially the short stature homeobox (SHOX) and arylsulfatase (ARSE) genes.[] For 8 of the 11 subjects, SRT was improved between 0.37 and 1.70 dB. Three of the 11 subjects showed deteriorations between 1.22 and 3.24 dB SRT.[]

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