M. Donlin

发表

Tissue-specific accumulation of MURB, a protein encoded by MuDR, the autonomous regulator of the Mutator transposable element family.

M. Freeling, D. Lisch, M. Donlin, 1995, The Plant cell.

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Amy Bernard, D. Beier, M. Donlin, 2013, Human molecular genetics.

Targeting RAD51 phosphotyrosine-315 to prevent unfaithful recombination repair in BCR-ABL1 leukemia.

T. Skorski, M. Nieborowska-Skorska, A. Słupianek, 2011, Blood.

Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly

K. Sund, K. Kaufman, E. Schorry, 2017, bioRxiv.

A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia.

S. Brugmann, K. Sund, H. Saal, 2015, Human Molecular Genetics.

Functional analysis of deletion derivatives of the maize transposon MuDR delineates roles for the MURA and MURB proteins.

L. Girard, M. Freeling, D. Lisch, 1999, Genetics.

Targeting RAD 51 phosphotyrosine-315 to prevent unfaithful recombination repair in BCR-ABL 1 leukemia

T. Skorski, M. Nieborowska-Skorska, A. Słupianek, 2011 .

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Amy Bernard, D. Beier, M. Donlin, 2013, Human molecular genetics.

A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia.

S. Brugmann, K. Sund, H. Saal, 2015, Human molecular genetics.