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FERMT1 gene
Known as:
C20ORF42
, kindlin-1
, CHROMOSOME 20 OPEN READING FRAME 42
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National Institutes of Health
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Related topics
Related topics
1 relation
Chromosomes, Human, Pair 20
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
The extreme C-terminal region of kindlin-2 is critical to its regulation of integrin activation
Jamila Hirbawi
,
K. Białkowska
,
+4 authors
E. Plow
Journal of Biological Chemistry
2017
Corpus ID: 2431402
Kindlin-2 (K2), a 4.1R-ezrin-radixin-moesin (FERM) domain adaptor protein, mediates numerous cellular responses, including…
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2015
2015
Full length talin stimulates integrin activation and axon regeneration
Chin Lik Tan
,
Jessica C. F. Kwok
,
Janosch P. Heller
,
Rong-Rong Zhao
,
R. Eva
,
J. Fawcett
Molecular and Cellular Neuroscience
2015
Corpus ID: 6899724
2014
2014
Kindler syndrome in mice and men
Elizabeth K Duperret
,
T. Ridky
Cancer Biology & Therapy
2014
Corpus ID: 28901456
Kindler syndrome (KS) in humans is a severe skin blistering disease associated with inflammation and increased risk of epidermal…
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2013
2013
Kindlin-1 regulates mitotic spindle formation by interacting with integrins and Plk-1
H. Patel
,
Judith Zich
,
+4 authors
V. Brunton
Nature Communications
2013
Corpus ID: 2872504
Kindlin-1 binds to integrins and regulates integrin activation at cell adhesions. Here we report a new function of Kindlin-1 in…
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2012
2012
Molecular Pathogenesis of Genetic and Inherited Diseases Partial Loss of Epithelial Phenotype in Kindlin-1 – Deficient Keratinocytes
Haiyan Qu
,
Tingting Wen
,
M. Pesch
,
M. Aumailley
2012
Corpus ID: 44525217
Kindlin-1 is an adaptor protein that is expressed by most epithelial cells and has been implicated in integrin bidirectional…
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Review
2009
Review
2009
Kindler-Syndrom
C. Has
Der Hautarzt
2009
Corpus ID: 209186847
ZusammenfassungDas Kindler-Syndrom ist eine neue Form der Epidermolysis bullosa hereditaria und die erste Genodermatose, die…
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Review
2005
Review
2005
Kindler surprise: mutations in a novel actin-associated protein cause Kindler syndrome.
S. White
,
W. McLean
Journal of dermatological science (Amsterdam)
2005
Corpus ID: 21505490
Review
2004
Review
2004
Kindler syndrome
G. Ashton
Clincal and Experimental Dermatology
2004
Corpus ID: 6416657
Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by…
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2004
2004
Gene symbol: Kind1. Disease: kindler syndrome.
C. Lanschuetzer
,
W. Muss
,
+4 authors
H. Hintner
Human Genetics
2004
Corpus ID: 8431950
1994
1994
II. Yeast sequencing reports. A 12·5 kb fragment of the yeast chromosome II contains two adjacent genes encoding ribosomal proteins and six putative new genes, one of which encodes a putative…
N. Démolis
,
L. Mallet
,
M. Jacquet
1994
Corpus ID: 25108294
The nucleotide sequence of a 12·5 kb fragment localized to the right arm of chromosome II of Saccharomyces cerevisiae has been…
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