|
🐜
|
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
20 auth.
S. Reid,
D. Schindler,
H. Hanenberg,
K. Barker,
S. Hanks,
R. Kalb,
K. Neveling,
P. Kelly,
S. Seal,
M. Freund,
...
M. Wurm,
S. Batish,
Francis P. Lach,
S. Yetgin,
H. Neitzel,
H. Ariffin,
M. Tischkowitz,
C. Mathew,
A. Auerbach,
N. Rahman
|
9 |
2007 |
9
🐜
|
|
🐜
|
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency.
16 auth.
M. O’Driscoll,
K. Cerosaletti,
Pierre-Marie Girard,
Yan Dai,
M. Stumm,
B. Kysela,
B. Hirsch,
A. Gennery,
S. Palmer,
J. Seidel,
...
R. Gatti,
Raymonda Varon,
M. Oettinger,
H. Neitzel,
P. Jeggo,
P. Concannon
|
8 |
2001 |
8
🐜
|
|
🦁
|
A routine method for the establishment of permanent growing lymphoblastoid cell lines
H. Neitzel
|
8 |
1986 |
8
🦁
|
|
🐬
|
Establishment and Characterization of an Immortalized Human Sebaceous Gland Cell Line (SZ95)1
C. Zouboulis,
H. Seltmann,
H. Neitzel,
C. Orfanos
|
8 |
1999 |
8
🐬
|
|
🐜
|
Regulation of mitotic entry by microcephalin and its overlap with ATR signalling
8 auth.
Gemma K. Alderton,
Laura Galbiati,
E. Griffith,
K. H. Surinya,
H. Neitzel,
A. Jackson,
...
P. Jeggo,
M. O’Driscoll
|
7 |
2006 |
7
🐜
|
|
🐬
|
Establishment and characterization of an immortalized human sebaceous gland cell line (SZ95).
C. Zouboulis,
H. Seltmann,
H. Neitzel,
C. Orfanos
|
7 |
1999 |
7
🐬
|
|
🐜
|
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12
13 auth.
H. Schuster,
T. Wienker,
S. Bähring,
N. Bilginturan,
Hakan R Toka,
H. Neitzel,
Eva Jeschke,
O. Toka,
Dennis A Gilbert,
A. Lowe,
...
J. Ott,
H. Haller,
F. Luft
|
7 |
1996 |
7
🐜
|
|
🐢
|
Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor.
H. Tönnies,
S. Huber,
Jörn-Sven Kuhl,
A. Gerlach,
W. Ebell,
H. Neitzel
|
6 |
2003 |
6
🐢
|
|
🐜
|
Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human
14 auth.
S. Tierling,
N. Souren,
Jasmin Gries,
C. Loporto,
Marco Groth,
P. Lutsik,
H. Neitzel,
I. Utz-Billing,
G. Gillessen‐Kaesbach,
H. Kentenich,
...
G. Griesinger,
K. Sperling,
E. Schwinger,
J. Walter
|
6 |
2009 |
6
🐜
|
|
🐜
|
Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1
10 auth.
A. Tibelius,
J. Marhold,
H. Zentgraf,
C. Heilig,
H. Neitzel,
B. Ducommun,
...
A. Rauch,
A. Ho,
J. Bartek,
A. Krämer
|
6 |
2009 |
6
🐜
|
|
🦁
|
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive condition.
9 auth.
H. Neitzel,
L. Neumann,
D. Schindler,
Andreas Wirges,
H. Tönnies,
M. Trimborn,
...
A. Krebsová,
Reyk Richter,
K. Sperling
|
6 |
2002 |
6
🦁
|
