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erbb3 and erbb2 Are Essential for Schwann Cell Migration and Myelination in Zebrafish
9 auth.
D. Lyons,
Hans-Martin Pogoda,
Matthew G. Voas,
I. Woods,
B. Diamond,
Rebecca Nix,
...
Naomi Arana,
J. Jacobs,
W. S. Talbot
|
8 |
2005 |
8
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in vivo protein trapping produces a functional expression codex of the vertebrate proteome
18 auth.
K. Clark,
Darius Balciunas,
Hans-Martin Pogoda,
Yonghe Ding,
S. Westcot,
V. Bedell,
T. Greenwood,
Mark D. Urban,
Kimberly J. Skuster,
Andrew M. Petzold,
...
Jun Ni,
A. Nielsen,
A. Patowary,
V. Scaria,
S. Sivasubbu,
Xiaolei Xu,
M. Hammerschmidt,
S. Ekker
|
7 |
2011 |
7
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Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.
18 auth.
Kathrin Laue,
Hans-Martin Pogoda,
P. Daniel,
A. van Haeringen,
Y. Alanay,
Simon von Ameln,
Martin Rachwalski,
Tim Morgan,
M. Gray,
M. Breuning,
...
G. M. Sawyer,
A. Sutherland-Smith,
P. Nikkels,
C. Kubisch,
W. Bloch,
B. Wollnik,
M. Hammerschmidt,
S. Robertson
|
7 |
2011 |
7
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The zebrafish forkhead transcription factor FoxH1/Fast1 is a modulator of Nodal signaling required for organizer formation
Hans-Martin Pogoda,
L. Solnica-Krezel,
W. Driever,
D. Meyer
|
7 |
2000 |
7
🦁
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A genetic screen identifies genes essential for development of myelinated axons in zebrafish.
14 auth.
Hans-Martin Pogoda,
Nitzan Sternheim,
D. Lyons,
B. Diamond,
Thomas A. Hawkins,
I. Woods,
D. H. Bhatt,
C. Franzini-armstrong,
C. Dominguez,
Naomi Arana,
...
J. Jacobs,
Rebecca Nix,
J. Fetcho,
W. S. Talbot
|
7 |
2006 |
7
🦁
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🐜
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Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
50 auth.
G. Borck,
A. Rehman,
A. Rehman,
Kwanghyuk Lee,
Hans-Martin Pogoda,
Naseebullah Kakar,
S. Ameln,
S. Ameln,
N. Grillet,
M. Hildebrand,
Zubair M. Ahmed,
Zubair M. Ahmed,
G. Nürnberg,
M. Ansar,
S. Basit,
...
Q. Javed,
R. Morell,
Nabilah Nasreen,
A. Shearer,
Adeel Ahmad,
K. Kahrizi,
R. S. Shaikh,
R. S. Shaikh,
R. A. Ali,
Shaheen N. Khan,
I. Goebel,
I. Goebel,
N. Meyer,
W. Kimberling,
J. Webster,
D. Stephan,
D. Stephan,
M. Schiller,
M. Bahlo,
H. Najmabadi,
P. Gillespie,
P. Nürnberg,
B. Wollnik,
S. Riazuddin,
S. Riazuddin,
Richard J. H. Smith,
W. Ahmad,
U. Müller,
M. Hammerschmidt,
T. Friedman,
S. Riazuddin,
S. Leal,
J. Ahmad,
C. Kubisch,
C. Kubisch
|
6 |
2011 |
6
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A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
24 auth.
Simon von Ameln,
Geng Wang,
Redouane Boulouiz,
M. Rutherford,
Geoffrey M. Smith,
Yun Li,
Hans-Martin Pogoda,
G. Nürnberg,
Barbara Stiller,
A. Volk,
...
G. Borck,
Jason S. Hong,
R. Goodyear,
O. Abidi,
P. Nürnberg,
K. Hofmann,
G. Richardson,
M. Hammerschmidt,
T. Moser,
B. Wollnik,
C. Koehler,
M. Teitell,
A. Barakat,
C. Kubisch
|
6 |
2012 |
6
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|
|
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Monorail/Foxa2 regulates floorplate differentiation and specification of oligodendrocytes, serotonergic raphé neurones and cranial motoneurones
22 auth.
William H. J. Norton,
M. Mangoli,
Z. Lele,
Hans-Martin Pogoda,
B. Diamond,
S. Mercurio,
C. Russell,
H. Teraoka,
H. Stickney,
Gerd-Jörg Rauch,
...
C. Heisenberg,
C. Houart,
T. Schilling,
Hans-Georg Frohnhoefer,
S. Rastegar,
C. Neumann,
R. Gardiner,
U. Strähle,
R. Geisler,
M. Rees,
W. S. Talbot,
Stephen W. Wilson
|
6 |
2005 |
6
🐜
|
|
🐜
|
Analysis of the reticulon gene family demonstrates the absence of the neurite growth inhibitor Nogo-A in fish.
7 auth.
H. Diekmann,
Michael Klinger,
T. Oertle,
D. Heinz,
Hans-Martin Pogoda,
M. Schwab,
...
C. Stuermer
|
6 |
2005 |
6
🐜
|
|
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Molecular genetics of pituitary development in zebrafish.
Hans-Martin Pogoda,
M. Hammerschmidt
|
6 |
2007 |
6
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|
