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 uBio  Web Results 91 - 100 of about 493

Synonyms:
   Tylosis jimenezi 
   Tylosis jimenezii 

Broader Terms:
   Tylosis 
 
 


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91.  Focal palmar keratoderma and leukokeratosis anogenitalis: an extremely rare genodermatosis associated with cytokeratine 17 mutation.LinkIT
Nantel-Battista M, Friedmann D, Kokta V, Bouffard D, Funaro D
Journal of the European Academy of Dermatology and Venereology : JEADV, 2015
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

92.  Highly prevalent SERPINB7 founder mutation causes pseudodominant inheritance pattern in Nagashima-type palmoplantar keratosis.LinkIT
Mizuno O, Nomura T, Suzuki S, Takeda M, Ohguchi Y, Fujita Y, Nishie W, Sugiura K, Akiyama M, Shimizu H
The British journal of dermatology, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

93.  iRHOM2-dependent regulation of ADAM17 in cutaneous disease and epidermal barrier function.LinkIT
Brooke MA, Etheridge SL, Kaplan N, Simpson C, O'Toole EA, Ishida-Yamamoto A, Marches O, Getsios S, Kelsell DP
Human molecular genetics, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

94.  Insights into desmosome biology from inherited human skin disease and cardiocutaneous syndromes.LinkIT
Nitoiu D, Etheridge SL, Kelsell DP
Cell communication & adhesion, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

95.  Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3.LinkIT
Kariminejad A, Barzegar M, Abdollahimajd F, Pramanik R, McGrath JA
Clinical and experimental dermatology, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

96.  Mutation p.Leu128Pro in the 1A domain of K16 causes pachyonychia congenita with focal palmoplantar keratoderma in a Chinese family.LinkIT
Dai L, Wu J, Guo H, Huang Y, Zhang K, Liu D, Fu L, Wu Y, Guan X, Bai Y, Liao Q
European journal of pediatrics, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

97.  Rhbdf2 mutations increase its protein stability and drive EGFR hyperactivation through enhanced secretion of amphiregulin.LinkIT
Hosur V, Johnson KR, Burzenski LM, Stearns TM, Maser RS, Shultz LD
Proceedings of the National Academy of Sciences of the United States of America, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

98.  Naegeli-Franceschetti-Jadassohn syndrome in a Saudi Arabian family.LinkIT
Tubaigy SM, Hassan HM
Journal of forensic sciences, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

99.  [Mutation analysis and prenatal diagnosis of keratin 9 gene in a large Chinese family with epidermolytic palmoplantar keratoderma].LinkIT
Liu N, Shi H, Kong X, Wu Q, Jiang M
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2014
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

100.  Diffuse non-epidermolytic palmoplantar keratoderma.LinkIT
Das A, Kumar D, Das NK
Indian pediatrics, 2013
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0



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