Genetic study of SMA patients without homozygous SMN 1 deletions: identification of compound … - Full text - MIT Libraries
Y Martin, A Valero, E del Castillo, S Pascual, C … - Human Genetics, 2002 - springerlink.com
... or repression of gene activity, depends on the interactions of YY1 with other ... E,
Wright M, Lush M, Wain H (2001) The HUGO Gene Nomenclature Committee (HGNC). ...
Cited by 9 - Web Search - ncbi.nlm.nih.gov

Composition-sensitive analysis of the human genome for regulatory signals - Full text - MIT Libraries
OV Kel-Margoulis, D Tchekmenev, AE Kel, E … - In Silico Biology, 2003 - iospress.metapress.com
... extracts from publicly available databases LocusLink and UniGene [Wheeler et al.,
2002], HGNC [Povey et al ... V$YY1_01 M00059 YY1 CCATNTWNNNW 44.4 17 7,90 0.96 ...
Cited by 11 - Web Search - bioinfo.de - tbiomed.com - ncbi.nlm.nih.gov - all 6 versions »

DNA polymorphisms in potential regulatory elements of the CFTR gene alter transcription factor … - Full text - MIT Libraries
R Rowntree, A Harris - Human Genetics, 2002 - springerlink.com
... E, Wright M, Lush M, Wain H (2001) The HUGO Gene Nomenclature Committee (HGNC). ... M
(2000) A naturally occurring sequence variation that creates a YY1 element is ...
Cited by 6 - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Genetics Home Reference;
JA Mitchell, RA Logan - lhncbc.nlm.nih.gov
... mining information from existing research, clinical, and consumer databases such
as Entrez Gene [2], HUGO Gene Nomenclature Committee (HGNC) [18], MedlinePlus ...
View as HTML - Web Search