Badam Enkhmandakh

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

Badam Enkhmandakh, Aleksandr V. Makeyev, Lkhamsuren Erdenechimeg et al. · Proceedings of the National Academy of Sciences · 2008 · 124 citations · Full text

Genomic Organization of the Genes Gtf2ird1, Gtf2i, and Ncf1 at the Mouse Chromosome 5 Region Syntenic to the Human Chromosome 7q11.23 Williams Syndrome Critical Region

Dashzeveg Bayarsaihan, Judit Dunai, John M. Greally et al. · Genomics · 2002 · 41 citations

Chromatin, Human Chromosome 7Q11.23, Chromosome Dynamics +11

The role of the proline-rich domain of Ssdp1 in the modular architecture of the vertebrate head organizer

Badam Enkhmandakh, Alexandr V. Makeyev, Dashzeveg Bayarsaihan · Proceedings of the National Academy of Sciences · 2006 · 40 citations · Full text

Proline-rich Domain, Genetics, Molecular Biology +19

GTF2IRD2 is located in the Williams–Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix–loop–helix repeats

Aleksandr V. Makeyev, Lkhamsuren Erdenechimeg, Ognoon Mungunsukh et al. · Proceedings of the National Academy of Sciences · 2004 · 31 citations · Full text

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development

Dashzeveg Bayarsaihan, Natalia Bitchevaia, Badam Enkhmandakh et al. · Gene Expression Patterns · 2003 · 27 citations

Cell Lineage, Developmental Biology, Tfii-i Family +8