|
🐜
|
Biallelic Inactivation of BRCA2 in Fanconi Anemia
13 auth.
N. Howlett,
T. Taniguchi,
S. Olson,
B. Cox,
Q. Waisfisz,
C. D. de Die-Smulders,
Nicole Persky,
M. Grompe,
H. Joenje,
G. Pals,
...
H. Ikeda,
E. Fox,
A. D’Andrea
|
10 |
2002 |
10
🐜
|
|
🐜
|
A novel ubiquitin ligase is deficient in Fanconi anemia
13 auth.
A. R. Meetei,
J. Winter,
A. Medhurst,
M. Wallisch,
Q. Waisfisz,
H. V. D. Vrugt,
A. Oostra,
Zhijiang Yan,
Chen Ling,
C. Bishop,
...
M. Hoatlin,
H. Joenje,
Weidong Wang
|
9 |
2003 |
9
🐜
|
|
🦁
|
The emerging genetic and molecular basis of Fanconi anaemia
H. Joenje,
K. J. Patel
|
9 |
2001 |
9
🦁
|
|
🐜
|
Disruption of the Fanconi anemia–BRCA pathway in cisplatin-sensitive ovarian tumors
8 auth.
T. Taniguchi,
M. Tischkowitz,
N. Ameziane,
S. Hodgson,
C. Mathew,
H. Joenje,
...
S. Mok,
A. D’Andrea
|
9 |
2003 |
9
🐜
|
|
🐢
|
Doxorubicin (adriamycin): a critical review of free radical-dependent mechanisms of cytotoxicity.
H. Keizer,
H. Pinedo,
G. Schuurhuis,
H. Joenje
|
8 |
1990 |
8
🐢
|
|
🐜
|
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
14 auth.
B. Xia,
J. Dorsman,
N. Ameziane,
Y. Vries,
M. Rooimans,
Qing Sheng,
G. Pals,
A. Errami,
E. Gluckman,
Julián Llera,
...
Weidong Wang,
D. Livingston,
H. Joenje,
J. Winter
|
8 |
2007 |
8
🐜
|
|
🐢
|
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
16 auth.
M. Levitus,
Q. Waisfisz,
B. Godthelp,
Y. Vries,
S. Hussain,
W. Wiegant,
Elhaam Elghalbzouri-Maghrani,
Jûrgen Steltenpool,
M. Rooimans,
G. Pals,
...
F. Arwert,
C. Mathew,
M. Zdzienicka,
K. Hiom,
J. Winter,
H. Joenje
|
8 |
2005 |
8
🐢
|
|
🐜
|
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
14 auth.
A. R. Meetei,
A. Medhurst,
Chen Ling,
Yutong Xue,
T. R. Singh,
Patrick Bier,
Jûrgen Steltenpool,
S. Stone,
I. Dokal,
C. Mathew,
...
M. Hoatlin,
H. Joenje,
J. Winter,
Weidong Wang
|
8 |
2005 |
8
🐜
|
|
🐢
|
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
20 auth.
J. R. Foe,
M. Rooimans,
L. Bosnoyan-Collins,
N. Alon,
M. Wijker,
L. Parker,
J. Lightfoot,
M. Carreau,
D. Callen,
A. Savoia,
...
N. C. Cheng,
C. V. Berkel,
M. Strunk,
J. Gille,
G. Pals,
F. Kruyt,
J. Pronk,
F. Arwert,
M. Buchwald,
H. Joenje
|
8 |
1996 |
8
🐢
|
|
🐢
|
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion
13 auth.
H. Vega,
Q. Waisfisz,
M. Gordillo,
N. Sakai,
I. Yanagihara,
M. Yamada,
D. Gosliga,
H. Kayserili,
Chengzhe Xu,
K. Ozono,
...
E. Jabs,
K. Inui,
H. Joenje
|
8 |
2005 |
8
🐢
|
|
🐜
|
A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome
8 auth.
A. R. Meetei,
S. Sechi,
M. Wallisch,
Dafeng Yang,
Mary K. Young,
H. Joenje,
...
M. Hoatlin,
Weidong Wang
|
8 |
2003 |
8
🐜
|
|
🐢
|
The Fanconi anaemia group G gene FANCG is identical with XRCC9
16 auth.
J. Winter,
Q. Waisfisz,
M. Rooimans,
C. V. Berkel,
L. Bosnoyan-Collins,
N. Alon,
M. Carreau,
O. Bender,
I. Demuth,
D. Schindler,
...
J. Pronk,
F. Arwert,
H. Hoehn,
M. Digweed,
M. Buchwald,
H. Joenje
|
8 |
1998 |
8
🐢
|
