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The following term was not found in PubMed: sefian
Page 1
Showing results for mosome sefian
Your search for Masome Sofian retrieved no results
Cytogenetic abnormalities in 42 rhabdomyosarcoma: a United Kingdom Cancer Cytogenetics Group Study.
Gordon T, McManus A, Anderson J, Min T, Swansbury J, Pritchard-Jones K, Shipley J; United kingdom Children's Cancer Study Group; United Kingdom Cancer Cytogenetics Group. Gordon T, et al. Med Pediatr Oncol. 2001 Feb;36(2):259-67. doi: 10.1002/1096-911X(20010201)36:2<259::AID-MPO1063>3.0.CO;2-K. Med Pediatr Oncol. 2001. PMID: 11452933
Molecular evidence for the PAX3/7-FKHR fusion genes was available for five ERMS and seven ARMS cases and compiled with the karyotypes. RESULTS: Clonal chro mosome aberrations were characterized for 25 ERMS and 17 ARMS cases. Thirty-six percent of the ERMS cases involved tr …
Molecular evidence for the PAX3/7-FKHR fusion genes was available for five ERMS and seven ARMS cases and compiled with the karyotypes. RESUL …
The genomic organization of Isopeptidase T-3 (ISOT-3), a new member of the ubiquitin specific protease family (UBP).
Timms KM, Ansari-Lari MA, Morris W, Brown SN, Gibbs RA. Timms KM, et al. Gene. 1998 Sep 14;217(1-2):101-6. doi: 10.1016/s0378-1119(98)00341-2. Gene. 1998. PMID: 9841226
A novel Isopeptidase T gene (ISOT-3) has been identified on human mosome 3q26.2--q26.3. gene shows 67.3% nucleotide identity and 54.8% amino acid identity to n Isopeptidase (ISOT-1). ...
A novel Isopeptidase T gene (ISOT-3) has been identified on human mosome 3q26.2--q26.3. gene shows 67.3% nucleotide identity and 54.8 …
Identification of a novel member of the snail/Gfi-1 repressor family, mlt 1, which is methylated and silenced in liver tumors of SV40 T antigen transgenic mice.
Tateno M, Fukunishi Y, Komatsu S, Okazaki Y, Kawai J, Shibata K, Itoh M, Muramatsu M, Held WA, Hayashizaki Y. Tateno M, et al. Cancer Res. 2001 Feb 1;61(3):1144-53. Cancer Res. 2001. PMID: 11221845
Shotgun sequencing of a bacterial artificial chro mosome clone containing this spot/locus was performed to identify genes within this region. ...
Shotgun sequencing of a bacterial artificial chro mosome clone containing this spot/locus was performed to identify genes within this …
18q deletion is difficult to detect by prenatal diagnosis: a report of two cases and a discussion of the literature.
Wu X, Zhu XY, Li J. Wu X, et al. Clin Exp Obstet Gynecol. 2017;44(1):151-153. Clin Exp Obstet Gynecol. 2017. PMID: 29714888 Review.
Fetuses with 18q deletion have few structural abnormalities, therefore ultrasound is unlikely to detect this anomaly. Prenatal chro- mosome microarray is a powerful tool in detecting subtle cytogenetic abnormalities such as 18q deletion....
Fetuses with 18q deletion have few structural abnormalities, therefore ultrasound is unlikely to detect this anomaly. Prenatal chro- moso …
[Genetic analysis and molecular mapping of a high-tillering mutant (ht1) in rice.].
Li WC, Wang YF, Ma SM, Guo SW. Li WC, et al. Yi Chuan. 2010 Oct;32(10):1065-70. doi: 10.3724/sp.j.1005.2010.01065. Yi Chuan. 2010. PMID: 20943495 Chinese.
By means of molecular marker technique, the HT1 gene was mapped to an interval between two SSR markers RM25435 and RM25552 on chro-mosome 10. Through high-resolution linkage analysis, the HT1 gene was further restricted to a 0.1 cM region flanked by two SSR markers RM25523 …
By means of molecular marker technique, the HT1 gene was mapped to an interval between two SSR markers RM25435 and RM25552 on chro-mosome …