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Synonyms:
   Tylosis 

Broader Terms:
   Cerambycidae (round-headed wood-borers) 
   Trachyderina 

More Specific:
   Tylosis angusticollis 
   Tylosis argus 
   Tylosis bifasciata 
   Tylosis conjuncta 
   Tylosis dimidiata 
   Tylosis hilaris 
   Tylosis jimenezi 
   Tylosis jimenezii 
   Tylosis jiminezi 
   Tylosis maculata 
   Tylosis maculatus 
   Tylosis oculata 
   Tylosis oculatus 
   Tylosis puncticollis 
   Tylosis robusta 
   Tylosis sellata 
   Tylosis sellatus 
   Tylosis sexualis 
   Tylosis suturalis 
   Tylosis triangularis 
 
 
Latest Articles on Tylosis Leconte 1850 from uBioRSS
Ladybird with lunch - An Inordinate Fondness for Beetles Photo Pool
Therates latreillei (Thomson 1860) - An Inordinate Fondness for Beetles Photo Pool


External Resources:



1.  Diagnosis and Management of Inherited Palmoplantar Keratodermas.LinkIT
Thomas BR, O'Toole EA
Acta dermato-venereologica, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

2.  Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma.LinkIT
Harjama L, Kettunen K, Elomaa O, Einarsdottir E, Heikkilä H, Kivirikko S, Lappalainen K, Saarela J, Alby C, Ranki A, Kere J, Hadj-Rabia S, Hannula-Jouppi K
Acta dermato-venereologica, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

3.  Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia.LinkIT
Wei H, Wee LWY, Born B, Seang S, Koh MJA, Yee R, Lin G, Rafi'ee K, Mey S, Tan EC
American journal of medical genetics. Part A Am. J. Med. Genet. A Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia. 296-302 10.1002/ajmg.a.61447 Haim-Munk syndrome (HMS) and Papillon-Lefevre syndrome (PLS) are phenotypic variants of palmoplantar keratoderma (PPK) with progressive early-onset periodontitis and dental caries. HMS and PLS have been associated with homozygous or compound heterozygous mutations in the lysosomal protease gene Cathepsin C (CTSC). There have been only a few documented cases of CTSC mutations in patients from South-East Asia. We report the clinical findings of two Cambodian brothers who presented with diffuse, demarcated PPK with transgrediens extending to the elbows and knees, as well as pachyonychia and dental caries. Arachnodactyly and periodontitis were also found in the older brother. Next-generation sequencing unveiled a homozygous missense variant in CTSC (NM_001814.5: c.1337AC: p.(Asp446Ala)) in both brothers. Both parents were heterozygous for the variant, while an unaffected older brother was homozygous for the wild-type allele. Our study adds to the spectrum of mutations and associated clinical presentations for this rare genodermatosis. © 2019 Wiley Periodicals, Inc. Wei Heming H Research Laboratory, KK Women's & Children's Hospital, Singapore. Wee Lynette W Y LWY Dermatology Service, KK Women's & Children's Hospital, Singapore. Born Bori B Department of Dermatology, Preah Kossamak Hospital, Phnom Penh, Cambodia. Seang Sokheng S Department of Dermatology, Preah Kossamak Hospital, Phnom Penh, Cambodia. Koh Mark J A MJA 0000-0002-4136-4105 Dermatology Service, KK Women's & Children's Hospital, Singapore. Paediatrics Academic Clinical Programme, SingHealth Duke-NUS Graduate Medical School, Singapore. Yee Ruixiang R Dental Service, KK Women's & Children's Hospital, Singapore. Lin Grace G Research Laboratory, KK Women's & Children's Hospital, Singapore. Rafi'ee Khadijah K Research Laboratory, KK Women's & Children's Hospital, Singapore. Mey Sithach S Department of Dermatology, Preah Kossamak Hospital, Phnom Penh, Cambodia. Tan Ene-Choo EC 0000-0001-5497-6058 Research Laboratory, KK Women's & Children's Hospital, Singapore. Paediatrics Academic Clinical Programme, SingHealth Duke-NUS Graduate Medical School, Singapore. eng NMRC/CG/M003/2017 National Medical Research Council International Case Reports Research Support, Non-U.S. Gov't Journal Article 2019 12 17 United States Am J Med Genet A 101235741 1552-4825 IM Haim-Munk syndrome Papillon-Lefevre syndrome cathepsin C palmoplantar keratoderma periodontitis 2019 09 19 2019 11 22 2019 11 26 2019 12 18 6 0 2019 12 18 6 0 2019 12 18 6 0 ppublish 31846207 10.1002/ajmg.a.61447 REFERENCES, 2020</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>4.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Novel mutation in the DSG1 gene causes autosomal-dominant striate palmoplantar keratoderma in a large Syrian family.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Abi Zamer B, Mahfood M, Saleh B, Al Mutery AF, Tlili A<br><font color=gray><i>Annals of human genetics Ann. Hum. Genet. Novel mutation in the DSG1 gene causes autosomal-dominant striate palmoplantar keratoderma in a large Syrian family. 472-476 10.1111/ahg.12335 Palmoplantar keratoderma (PPK) is a heterogenous group of skin disorders characterized by a persistent thickening of the palms of the hands and sometimes soles of the feet. PPK can be classified into many types, including diffuse, transgradient, and focal or striate, where the areas of palmoplantar skin are alternatively thickened. Mutations in four main genes, keratin 9 (KRT9), keratin 1 (KRT1), desmoglein (DSG1), and desmoplakin (DSP), have been associated with PPK. Striate PPK (SPPK) is commonly caused by mutations in DSG1. However, DSP and KRT1 gene mutations have been identified in some cases. In this study, fragment and sequencing analysis were performed for a large Syrian family with dominant SPPK. Segregation analysis showed a linkage with DSG1 gene. Direct Sanger sequencing identified a new mutation c.dup165_168AGCA. This frameshift mutation was heterozygous in all affected family members and absent in all normal individuals. © 2019 John Wiley & Sons Ltd/University College London. Abi Zamer Batoul B Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates. Mahfood Mona M Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates. Saleh Batoul B Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates. Al Mutery Abdullah Fahd AF Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates. Molecular Genetics Research Laboratory, University of Sharjah, Sharjah, United Arab Emirates. Tlili Abdelaziz A 0000-0002-8039-3013 Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates. Molecular Genetics Research Laboratory, University of Sharjah, Sharjah, United Arab Emirates. eng University of Sharjah International Journal Article Research Support, Non-U.S. Gov't 2019 06 13 England Ann Hum Genet 0416661 0003-4800 IM DSG1 gene Striate Palmoplantar keratoderma dominant mutation linkage analysis 2019 01 20 2019 04 15 2019 05 16 2019 6 14 6 0 2019 6 14 6 0 2019 6 14 6 0 ppublish 31192455 10.1111/ahg.12335 REFERENCES, 2019</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>5.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Liu X, Qiu C, He R, Zhang Y, Zhao Y<br><font color=gray><i>Molecular genetics & genomic medicine, 2019</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>6.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Evaluation and Management of Premalignant Conditions of the Esophagus: A Systematic Survey of International Guidelines.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Ramai D, Lai JK, Ofori E, Linn S, Reddy M<br><font color=gray><i>Journal of clinical gastroenterology, 2019</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>7.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Hereditary Palmoplantar Keratoderma: A Practical Approach to the Diagnosis.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Dev T, Mahajan VK, Sethuraman G<br><font color=gray><i>Indian dermatology online journal, 2020</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>8.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Exome sequencing identifies a KRT9 pathogenic variant in a Chinese pedigree with epidermolytic palmoplantar keratoderma.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Li C, Chen P, Sun S, Zeng K, Liang J, Wang Q, Zhang S, Xu M, Li Z, Zhang X<br><font color=gray><i>Molecular genetics & genomic medicine, 2019</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>9.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Whole Exome Sequencing Identified a Novel Mutation of the RHBDF2 Gene in a Chinese Family of Tylosis with Esophageal Cancer.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Qu L, Sha S, Zou QL, Gao XH, Xiao T, Chen HD, He CC<br><font color=gray><i>Acta dermato-venereologica, 2019</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br>10.  <a href=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 class=title>Uncommon Endoscopic Findings in a Tylosis Patient: A Case Report.</a><a href=http://ubio.org/tools/linkit.php?map%5B%5D=all&link_type=2&url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0><img src=linkit.png border=0 title='LinkIT' alt='LinkIT'></a> <br><span class=j>Surapaneni BK, Kancharla P, Vinayek R, Dutta SK, Goldfinger M<br><font color=gray><i>Case reports in oncology, 2020</i></font><br><font color=#008000>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0<br></font></span><br><br><br><table cellspacing=0 cellpadding=0 align=center><tr valign=bottom><td align=center><img src=p.png border=0></td><td align=center><img src=o_red.png border=0></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=2><img src=o_yellow.png border=0></a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=3><img src=o_yellow.png border=0></a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=4><img src=o_yellow.png border=0></a></td><td align=center><a 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href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=2><img src=rtal.png border=0></a></td></tr><td align=center></td><td align=center>1</td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=2>2</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=3>3</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=4>4</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=5>5</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=6>6</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=7>7</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=8>8</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=9>9</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=10>10</a></td><td align=center><a href=http://ubio.org/portal/index.php?search=Tylosis+Leconte+1850&category=l&client=pubmed&startPage=2>»</a></td></tr></table></table></tr></table></td><script src="http://www.google-analytics.com/urchin.js" type="text/javascript"> </script> <script type="text/javascript"> _uacct = "UA-634822-1"; urchinTracker(); </script> </BODY> </HTML>