L. Ma

发表

Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).

S. Humbert, J. Hoeijmakers, W. Vermeulen, 1994, The EMBO journal.

Genetic interactions between error-prone and error-free postreplication repair pathways in Saccharomyces cerevisiae.

W. Xiao, S. Bacchetti, B. L. Chow, 1999, Mutation research.

The xeroderma pigmentosum group B protein ERCC3 produced in the baculovirus system exhibits DNA helicase activity.

A. van der Eb, L. Ma, E. D. Siemssen, 1994, Nucleic acids research.

Human cytosolic sulphotransferases: genetics, characteristics, toxicological aspects.

H. Glatt, H. Boeing, W. Meinl, 2001, Mutation research.

Mammalian nucleotide excision repair.

J. Hoeijmakers, A. van der Eb, L. Ma, 1995, Biochimica et biophysica acta.

Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function

A. Jochemsen, J. Hoeijmakers, A. van der Eb, 1994, Molecular and cellular biology.

The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor.

L. J. Veer, J. Hoeijmakers, W. Vermeulen, 1997, Nucleic acids research.

Exome sequencing identifies highly recurrent somatic GATA2 and CEBPA mutations in acute erythroid leukemia

Q. Wang, Y. Xu, A. Sun, 2015, Leukemia.

A point mutation of zebrafish c-cbl gene in the ring finger domain produces a phenotype mimicking human myeloproliferative disease

L. Zon, X. Liu, X. Peng, 2015, Leukemia.

Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.

J. Hoeijmakers, A. van der Eb, G. Weeda, 1991, Nucleic acids research.

Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndrome.

J. Hoeijmakers, A. van der Eb, D. Bootsma, 1991, Carcinogenesis.