scholarly journals Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning

1997 ◽  
Vol 61 (1) ◽  
pp. 111-119 ◽  
Author(s):  
Farideh Mirzayans ◽  
Alan J. Mears ◽  
Sun-Wei Guo ◽  
William G. Pearce ◽  
Michael A. Walter
Keyword(s):  
Chromosomal Region ◽  
Human Chromosomal Region

Seven polymorphic loci mapping to human chromosomal region 11q22-qter

Genomics ◽  
1988 ◽  
Vol 2 (1) ◽  
pp. 66-75 ◽  
Author(s):  
Cheryl L. Maslen ◽  
Carol Jones ◽  
Thomas Glaser ◽  
R.Ellen Magenis ◽  
Robert Sheehy ◽  
...  
Keyword(s):  
Chromosomal Region ◽  
Polymorphic Loci ◽  
Human Chromosomal Region

scholarly journals Cosmid clones from microdissected human chromosomal region 15q11–q13

1993 ◽  
Vol 38 (3) ◽  
pp. 267-275 ◽  
Author(s):  
Takaya Tohma ◽  
Toshiya Tamura ◽  
Tohru Ohta ◽  
Hidenobu Soejima ◽  
Takeo Kubota ◽  
...  
Keyword(s):  
Chromosomal Region ◽  
Human Chromosomal Region

Single Nucleotide Polymorphisms within the 8Q24 Region are Not Associated with the Risk of Intraductal Papillary Mucinous Neoplasms of the Pancreas

2016 ◽  
Vol 25 (3) ◽  
pp. 311-315 ◽  
Author(s):  
Nikola Panic ◽  
Alberto Larghi ◽  
Rosarita Amore ◽  
Roberta Pastorino ◽  
Milutin Bulajic ◽  
...  
Keyword(s):  
Chromosomal Region ◽  
Cancer Susceptibility ◽  
Nucleotide Polymorphisms ◽  
Intraductal Papillary Mucinous Neoplasms ◽  
Single Nucleotide ◽  
Mucinous Neoplasms ◽  
History Of ◽  
8Q24 Region ◽  
History Of Cancer ◽  
Human Chromosomal Region

Background & Aims: Intraductal papillary mucinous neoplasms (IPMNs) of the pancreas have been reported to be associated with an increased risk of developing extra-pancreatic malignancies. A common genetic background has been hypothesised to be responsible for such an association. Human chromosomal region 8q24 has been associated with many types of cancer. The majority of these associations lie at approximately 128 Mb on chromosome 8. We conducted a study in order to examine the association between IPMN and single nucleotide polymorphisms (SNPs) from the 8q24 region, namely rs10505477, rs6983267, rs7014346, rs6993464, previously reported to influence general cancer susceptibility. Methods. The study was performed on 117 IPMN cases and 231 controls. Cases were enrolled at the Digestive Endoscopy Unit, Policlinico Agostino Gemelli from January, 2010 to June, 2011, with either a prevalent or incident IPMN diagnosis. Status of SNPs was determined using a StepOne Real-time PCR system (Applied Biosystems) and TaqMan SNP Genotyping Assay™ 40X. Unconditional multiple logistic regression models were used to estimate odds ratios and 95% confidence intervals for the association of selected SNPs and IPMNs. Results. Cases were more likely to report a 1st degree family history of cancer (p<0.001), as well as heavy smoking (p=0.001) and heavy drinking habits (p<0.001). No significant association was observed between IPMN and selected SNPs. The results were confirmed also when stratified according to any 1st-degree family history of cancer. Conclusion. Patients with IPMN do not have a higher prevalence of SNPs in the human chromosomal region 8q24 in respect to the control population. Abbreviations: CASC8: cancer susceptibility candidate 8; CRC: colorectal cancer; ENPP2: ectonucleotide pyrophosphatase/phosphodiesterase 2; EPM: extra-pancreatic malignancy; eQTLs: expression quantitative trait loci; IPMN: intraductal papillary mucinous neoplasm; MYC: myelocytomatosis viral oncogene homolog gene; NOV: nephroblastoma over-expressed gene; PCR: polymerase chain reaction; POU5F1P1: POU class 5 homeobox 1 pseudogene 1 gene; S-MRCP: magnetic resonance cholangiopancreatography with secretin stimulation; SNP: single nucleotide polymorphism; TCF4: transcription factor 4.

Microdissection and Microcloning of Genomic DNA Markers from Human Chromosomal Region 11q23

Genomics ◽  
1993 ◽  
Vol 16 (1) ◽  
pp. 169-172 ◽  
Author(s):  
Naohiko Seki ◽  
Masatake Yamauchi ◽  
Toshiyuki Saito ◽  
Reiko Katakura ◽  
Tohru Ohta ◽  
...  
Keyword(s):  
Dna Markers ◽  
Genomic Dna ◽  
Chromosomal Region ◽  
Human Chromosomal Region

Cosmid mapping and locus linkage within the human chromosomal region 22q13.1

1993 ◽  
Vol 70 (2) ◽  
pp. 108-111 ◽  
Author(s):  
Nikolaus Blin ◽  
Roman Müllenbach ◽  
Ron Suijkerbuijk ◽  
Ruth Herzog ◽  
Eckart Meese
Keyword(s):  
Chromosomal Region ◽  
Human Chromosomal Region

Assignment of β-hexosaminidase A α-subunit to human chromosomal region 15q23→q24

1991 ◽  
Vol 56 (3-4) ◽  
pp. 164-164 ◽  
Author(s):  
H. Nakai ◽  
M.G. Byers ◽  
N.J. Nowak ◽  
T.B. Shows
Keyword(s):  
Chromosomal Region ◽  
Alpha Subunit ◽  
Hexosaminidase A ◽  
Human Chromosomal Region

Sequential expression in the nervous system of C-MYB andVIP genes, located in human chromosomal region 6q24

1987 ◽  
Vol 13 (4) ◽  
pp. 305-313 ◽  
Author(s):  
I. Gozes ◽  
H. Nakai ◽  
M. Byers ◽  
R. Avidor ◽  
Y. Weinstein ◽  
...  
Keyword(s):  
Nervous System ◽  
Chromosomal Region ◽  
Human Chromosomal Region

The gene for insulin-like growth factor-binding protein-1 is localized to human chromosomal region 7p14-p12

Genomics ◽  
1990 ◽  
Vol 6 (3) ◽  
pp. 413-418 ◽  
Author(s):  
Jonas Ekstrand ◽  
Ewa Ehrenborg ◽  
Ingrid Stern ◽  
Birgitta Stellan ◽  
Lore Zech ◽  
...  
Keyword(s):  
Growth Factor ◽  
Chromosomal Region ◽  
Binding Protein ◽  
Insulin Like Growth Factor ◽  
Factor Binding ◽  
Human Chromosomal Region
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