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 uBio  Web Results 81 - 90 of about 493

Synonyms:
   Tylosis jimenezi 
   Tylosis jimenezii 

Broader Terms:
   Tylosis 
 
 


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81.  A spontaneous KRT16 mutation in a dog breed: a model for human focal non-epidermolytic palmoplantar keratoderma (FNEPPK).LinkIT
Plassais J, Guaguère E, Lagoutte L, Guillory AS, de Citres CD, Degorce-Rubiales F, Delverdier M, Vaysse A, Quignon P, Bleuart C, Hitte C, Fautrel A, Kaerle C, Bellaud P, Bensignor E, Queney G, Bourrat E, Thomas A, André C
The Journal of investigative dermatology, 2015
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

82.  [Ainhum and "African acral keratoderma": three cases].LinkIT
Koudoukpo C, Bourrat E, Rausky J, Yédomon H, Bagot M, Blanchet-Bardon C, Petit A
Annales de dermatologie et de venereologie, 2015
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

83.  A gain-of-function mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family.LinkIT
He Y, Zeng K, Zhang X, Chen Q, Wu J, Li H, Zhou Y, Glusman G, Roach J, Etheridge A, Qing S, Tian Q, Lee I, Tian X, Wang X, Wu Z, Hood L, Ding Y, Wang K
The Journal of investigative dermatology, 2015
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

84.  Next-generation sequencing detection and characterization of a heterozygous novel splice junction mutation in the 2B domain of KRT1 in a family with diffuse palmoplantar keratoderma.LinkIT
Banerjee S, Ren Y, Wei T, Zhou Z, Yu P, Guan F, Wei X, Ye S, Yan S, Zheng M, Raff ML, Qi M
Experimental dermatology, 2015
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

85.  Effect of oxygen on the growth and biofilm formation of Xylella fastidiosa in liquid media.LinkIT
Shriner AD, Andersen PC
Current microbiology, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

86.  Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9.LinkIT
Guo Y, Shi M, Tan ZP, Shi XL
Genetics and molecular research : GMR, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

87.  KRT9 gene mutation as a reliable indicator in the prenatal molecular diagnosis of epidermolytic palmoplantar keratoderma.LinkIT
Ke HP, Jiang HL, Lv YS, Huang YZ, Liu RR, Chen XL, Du ZF, Luo YQ, Xu CM, Fan QH, Zhang XN
Gene, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

88.  A recurrent p.M157R mutation of keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma and literature review.LinkIT
Liang YH, Liu QX, Huang L, Zeng K
International journal of dermatology, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

89.  Nagashima-type palmoplantar keratosis: a common Asian type caused by SERPINB7 protease inhibitor deficiency.LinkIT
Kubo A
The Journal of investigative dermatology, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

90.  [Palmoplantar dermatoses: when should genes be considered?].LinkIT
Seebode C, Schiller S, Emmert S, Giehl K
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0



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