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Martin Oti

Showing results (31-40 of 35) with videos related to

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Molecular Cell|April 22, 2019
TAF5L and TAF6L Maintain Self-Renewal of Embryonic Stem Cells via the MYC Regulatory NetworkDavide Seruggia, Martin Oti, Pratibha Tripathi, et al.
Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
Plos Genetics|September 3, 2010
Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locusEvelyn N Kouwenhoven, Simon J van Heeringen, Juan J Tena, et al.
American Journal of Human Genetics|May 2, 2017
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian FamiliesThandiswa Ngcungcu, Martin Oti, Jan C Sitek, et al.
Disease Models & Mechanisms|January 10, 2017
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathyCelia Zazo Seco, Anna Castells-Nobau, Seol-Hee Joo, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Molecular Cell|April 22, 2019
TAF5L and TAF6L Maintain Self-Renewal of Embryonic Stem Cells via the MYC Regulatory NetworkDavide Seruggia, Martin Oti, Pratibha Tripathi, et al.
Plos Genetics|November 9, 2013
Human intellectual disability genes form conserved functional modules in DrosophilaMerel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, et al.
Plos Genetics|September 3, 2010
Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locusEvelyn N Kouwenhoven, Simon J van Heeringen, Juan J Tena, et al.
American Journal of Human Genetics|May 2, 2017
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian FamiliesThandiswa Ngcungcu, Martin Oti, Jan C Sitek, et al.
Disease Models & Mechanisms|January 10, 2017
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathyCelia Zazo Seco, Anna Castells-Nobau, Seol-Hee Joo, et al.
Pageof 4