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NDRG1 wt Allele
Known as:
TDD5
, PROXY1
, HMSNL
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Human NDRG1 wild-type allele is located in the vicinity of 8q24.3 and is approximately 60 kb in length. This allele, which encodes protein NDRG1, is…
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National Institutes of Health
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Related topics
Related topics
8 relations
8q24
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
Cell Differentiation process
Cell Proliferation
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Broader (1)
NDRG1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Identification and functional characterization of two missense mutations in NDRG1 associated with Charcot‐Marie‐Tooth disease type 4D
Li-Xi Li
,
Gonglu Liu
,
Zhi-Jun Liu
,
Cong Lu
,
Zhi-Ying Wu
Human Mutation
2017
Corpus ID: 40286212
Charcot‐Marie‐Tooth disease type 4D (CMT4D) is an autosomal‐recessive demyelinating form of CMT characterized by a severe distal…
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Highly Cited
2010
Highly Cited
2010
Ablation of the Kinase NDR1 Predisposes Mice to the Development of T Cell Lymphoma
H. Cornils
,
M. Stegert
,
+4 authors
B. Hemmings
Science Signaling
2010
Corpus ID: 20941059
The kinase NDR1 functions as a haploinsufficient tumor suppressor by ensuring proper apoptotic responses. Lymphoma from…
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2008
2008
Hereditary motor and sensory neuropathy Lom type in a Serbian family.
J. Dačković
,
M. Keckarević‐Marković
,
+6 authors
S. Apostolski
Acta myologica
2008
Corpus ID: 10838191
Hereditary motor and sensory neuropathy Lom type (HMSNL), also called CMT 4D, a hereditary autosomal recessive neuropathy, caused…
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2007
2007
Systemwide implications of the repeal of the national maximum speed limit.
D. Grabowski
,
M. Morrisey
Accident Analysis and Prevention
2007
Corpus ID: 39758843
Highly Cited
2005
Highly Cited
2005
The mechanism of cell adhesion by classical cadherins: the role of domain 1
O. Harrison
,
E. Corps
,
T. Berge
,
P. Kilshaw
Journal of Cell Science
2005
Corpus ID: 24557952
The mechanism by which classical cadherins mediate cell adhesion and, in particular, the roles played by calcium and Trp2, the…
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1998
1998
HMSNL in a 13-year-old Bulgarian girl
M. Baethmann
,
G. Göhlich-Ratmann
,
J. Schröder
,
L. Kalaydjieva
,
T. Voit
Neuromuscular Disorders
1998
Corpus ID: 23730920
1998
1998
Molecular evolution of an imprinted gene: repeatability of patterns of evolution within the mammalian insulin-like growth factor type II receptor.
Nick G.C. Smith
,
Laurence D. Hurst
Genetics
1998
Corpus ID: 20552538
The repeatability of patterns of variation in Ka/Ks and Ks is expected if such patterns are the result of deterministic forces…
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1998
1998
Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family
L. Merlini
,
M. Villanova
,
+6 authors
Luba Kalaydjieva
Neuromuscular Disorders
1998
Corpus ID: 326879
1991
1991
Characterization of the promoter region of the c-yes proto-oncogene: the importance of the GC boxes on its promoter activity.
Y. Matsuzawa
,
K. Semba
,
+4 authors
T. Yamamoto
Oncogene
1991
Corpus ID: 31348696
In this study we cloned the 5' flanking sequence of the human c-yes gene and identified its promoter region. A 0.53 kilobase pair…
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1990
1990
Thrombus imaging: a comparison of radiolabeled GC4 and T2G1s fibrin-specific monoclonal antibodies.
S. Rosebrough
,
J. McAfee
,
+6 authors
G. Gagne
Journal of Nuclear Medicine
1990
Corpus ID: 27200732
Radioimmunoimaging of experimentally-induced canine thrombi has previously been achieved with iodine-131- and indium-111-labeled…
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