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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.[ncbi.nlm.nih.gov]
Microarray analysis identified Hex (Hematopoietically expressed homeobox), a central transcription factor in vertebrate embryogenesis and liver development, as a novel CDCA[ncbi.nlm.nih.gov]
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[ncbi.nlm.nih.gov]
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Endometrioma
OBJECTIVE: To determine whether laparoscopic endometrioma resection alters peri-implantation endometrial HOXA-10, HOXA-11, LIF, ITGB3 and ITGAV mRNA expression.[ncbi.nlm.nih.gov]
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[ncbi.nlm.nih.gov]
CASE: An 11-year-old adolescent underwent an emergency operation for left ovarian endometrioma. Her menarche occurred spontaneously 6 months after surgery.[ncbi.nlm.nih.gov]
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Ambiguous Genitalia
Abstract We describe a patient with ambiguous genitalia, gonadoblastoma, aniridia, mental retardation and 46XY, del (11)(p13) karyotype.[ncbi.nlm.nih.gov]
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[ncbi.nlm.nih.gov]
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[ncbi.nlm.nih.gov]
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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.[ncbi.nlm.nih.gov]
[…] 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[ncbi.nlm.nih.gov]
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.[ncbi.nlm.nih.gov]
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Trigonocephaly
Abstract A seventh case of deletion of the distal long arm of a chromosome 11 is described.[ncbi.nlm.nih.gov]
Abstract This communication brings the number of recognized cases of the C (trigonocephaly) syndrome to 11.[ncbi.nlm.nih.gov]
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.[ncbi.nlm.nih.gov]
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Waardenburg Syndrome
Among these implantees, 11 were diagnosed with WS (0.59% of all implantees).[ncbi.nlm.nih.gov]
KEYWORDS: PAX3; arginine methylation; chromosomes; homeobox; homeodomain; mitosis; mitotic chromosome; mutant; protein arginine N-methyltransferase 5 (PRMT5); transcription[ncbi.nlm.nih.gov]
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[ncbi.nlm.nih.gov]
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Becker Muscular Dystrophy
Each of five patients had deletions of exons 11-27 in common.[ncbi.nlm.nih.gov]
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[ncbi.nlm.nih.gov]
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.[ncbi.nlm.nih.gov]
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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.[ncbi.nlm.nih.gov]
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.[ncbi.nlm.nih.gov]
The clinical features of the 11 patients were also investigated.[ncbi.nlm.nih.gov]
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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.[ncbi.nlm.nih.gov]
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.[ncbi.nlm.nih.gov]
After chemotherapy, PM disappearance was confirmed in 11 patients. Gastrectomy was eventually performed in 11 patients.[ncbi.nlm.nih.gov]
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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).[ncbi.nlm.nih.gov]
This interval encompasses several genes, especially the short stature homeobox (SHOX) and arylsulfatase (ARSE) genes.[ncbi.nlm.nih.gov]
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.[ncbi.nlm.nih.gov]