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SPINK5 gene
Known as:
NS
, LEKTI
, SPINK5
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National Institutes of Health
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Related topics
Related topics
3 relations
SPINK4 gene
SPINK5 protein, human
SPINK6 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome
S. Numata
,
K. Teye
,
+9 authors
T. Hashimoto
Experimental Dermatology
2016
Corpus ID: 205128467
A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in…
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2015
2015
NETosis in cancer
J. Cedervall
,
A. Olsson
Oncoscience
2015
Corpus ID: 5432730
A large proportion of cancer-related deaths are caused by thrombosis and general organ failure. Although the awareness of tumor…
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2014
2014
Heterogeneous and abnormal localization of desmosomal proteins in oral intraepithelial neoplasms.
S. Aizawa
,
Takanaga Ochiai
,
T. Ara
,
H. Yamada
,
H. Hasegawa
Journal of Oral Science
2014
Corpus ID: 13585985
To study the relationship between the biological and morphological characteristics of oral intraepithelial neoplasms (OINs), we…
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2013
2013
Netherton syndrome with multiple non-melanoma skin cancers.
E. V. D. van der Voort
,
E. Prens
Acta Dermato-Venereologica
2013
Corpus ID: 36867152
textabstractNetherton syndrome (NS) is a rare autosomal recessive genodermatosis caused by SPINK-5 mutations. The SPINK-5 gene…
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Review
2013
Review
2013
Netherton syndrome and its multifaceted defective protein LEKTI.
M. D’Alessio
,
P. Fortugno
,
G. Zambruno
,
A. Hovnanian
Giornale italiano di dermatologia e venereologia…
2013
Corpus ID: 895082
Netherton syndrome (NS, OMIM 256500) is a rare autosomal recessive disorder manifesting with congenital ichthyosis, a specific…
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2011
2011
Expression and regulation of murine SPINK12, a potential orthologue of human LEKTI2
K. Reiss
,
U. Meyer-Hoffert
,
+8 authors
R. Sedláček
Experimental Dermatology
2011
Corpus ID: 25529611
Abstract: A balanced proteolytic activity in the epidermis is vital to maintain epidermal homoeostasis and barrier function…
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2011
2011
[A lethal variant of Netherton syndrome in a large inbred family].
Y. Capri
,
P. Vanlieferinghen
,
B. Boeuf
,
P. Dechelotte
,
A. Hovnanian
,
B. Lecomte
Archives de pédiatrie
2011
Corpus ID: 24910468
2008
2008
LEKTI domain 15 is a functional Kazal-type proteinase inhibitor.
K. Vitzithum
,
T. Lauber
,
+4 authors
U. Marx
Protein Expression and Purification
2008
Corpus ID: 32717772
2005
2005
Netherton syndrome in two Japanese siblings with a novel mutation in the SPINK5 gene: immunohistochemical studies of LEKTI and other epidermal molecules
Y. Shimomura
,
N. Sato
,
N. Kariya
,
S. Takatsuka
,
M. Ito
British Journal of Dermatology
2005
Corpus ID: 26032029
Background Netherton syndrome (NS) is a severe autosomal recessive disorder characterized by ichthyosiform erythroderma, bamboo…
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Review
2002
Review
2002
Biochemical Features, Molecular Biology and Clinical Relevance of the Human 15-Domain Serine Proteinase Inhibitor LEKTI
M. Walden
,
P. Kreutzmann
,
K. Drögemüller
,
H. John
,
W. Forssmann
,
H. Mägert
Biological chemistry
2002
Corpus ID: 26084613
Abstract Based on the isolation of a 55 amino acid peptide from human hemofiltrate, we cloned the cDNA for a novel human 15…
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