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Genomics
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February 9, 2000
DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner
M P Scheer, S van der Maarel, S Kübart, et al.
Kidney International
|
January 1, 1997
Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie
F Hildebrandt, B Strahm, H G Nothwang, et al.
FEBS Letters
|
March 23, 1992
Structure and RNA content of the prosomes
O Coux, H G Nothwang, K Scherrer, et al.
Science (New York, N.Y.)
|
August 26, 1994
cDNA cloning and interferon gamma down-regulation of proteasomal subunits X and Y
K Akiyama, K Yokota, S Kagawa, et al.
HNO
|
April 10, 2019
[Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version]
J Schulze, L Nolte, S Lyutenski, et al.
Journal of Medical Genetics
|
April 6, 2001
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
G Borck, J Wirth, T Hardt, et al.
HNO
|
May 9, 2019
Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes
J Schulze, L Nolte, S Lyutenski, et al.
Molecular Biology Reports
|
January 1, 1990
The prosomes: molecular and cellular biology
K Scherrer, H G Nothwang, I S Pereira, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie
F Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
American Journal of Medical Genetics
|
February 24, 2001
Cosegregation of T108A Elk-1 with mental retardation
A Schröer, M P Scheer, S Zacharias, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 42) with videos related to
Sort By:
Page
of 5
Genomics
|
February 9, 2000
DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner
M P Scheer, S van der Maarel, S Kübart, et al.
Kidney International
|
January 1, 1997
Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie
F Hildebrandt, B Strahm, H G Nothwang, et al.
FEBS Letters
|
March 23, 1992
Structure and RNA content of the prosomes
O Coux, H G Nothwang, K Scherrer, et al.
Science (New York, N.Y.)
|
August 26, 1994
cDNA cloning and interferon gamma down-regulation of proteasomal subunits X and Y
K Akiyama, K Yokota, S Kagawa, et al.
HNO
|
April 10, 2019
[Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version]
J Schulze, L Nolte, S Lyutenski, et al.
Journal of Medical Genetics
|
April 6, 2001
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
G Borck, J Wirth, T Hardt, et al.
HNO
|
May 9, 2019
Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes
J Schulze, L Nolte, S Lyutenski, et al.
Molecular Biology Reports
|
January 1, 1990
The prosomes: molecular and cellular biology
K Scherrer, H G Nothwang, I S Pereira, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie
F Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
American Journal of Medical Genetics
|
February 24, 2001
Cosegregation of T108A Elk-1 with mental retardation
A Schröer, M P Scheer, S Zacharias, et al.
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of 5