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There are 15612 results for: content related to: A novel splice site mutation in NCSTN underlies a Japanese family with hidradenitis suppurativa

  1. You have full text access to this OnlineOpen article
    Genetic analysis of NCSTN for potential association with hidradenitis suppurativa in familial and nonfamilial patients

    British Journal of Dermatology

    Volume 175, Issue 2, August 2016, Pages: 414–416, M. Liu, J.W. Davis, K.B. Idler, N.M. Mostafa, M.M. Okun and J.F. Waring

    Version of Record online : 10 JUN 2016, DOI: 10.1111/bjd.14482

  2. Haploinsufficiency caused by a nonsense mutation in NCSTN underlying hidradenitis suppurativa in a Chinese family

    Clinical and Experimental Dermatology

    Volume 40, Issue 8, December 2015, Pages: 916–919, J.-q. Yang, X.-j. Wu, T.-t. Dou, T. Jiao, X.-b. Chen, M. Min, S.-q. Cai and M. Zheng

    Version of Record online : 30 JUL 2015, DOI: 10.1111/ced.12724

  3. Hidradenitis suppurativa: the role of immune dysregulation

    International Journal of Dermatology

    Volume 53, Issue 10, October 2014, Pages: 1186–1196, Genevieve Kelly, Cheryl M. Sweeney, Anne-Marie Tobin and Brian Kirby

    Version of Record online : 25 JUN 2014, DOI: 10.1111/ijd.12550

  4. A novel nicastrin mutation in a large Chinese family with hidradenitis suppurativa

    British Journal of Dermatology

    Volume 168, Issue 5, May 2013, Pages: 1141–1143, T. Jiao, H. Dong, L. Jin, S. Wang and J. Wang

    Version of Record online : 21 MAR 2013, DOI: 10.1111/bjd.12135

  5. Executive function and genetic predisposition to schizophrenia—the Maudsley family study

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 3, 5 April 2008, Pages: 285–293, P. Birkett, T. Sigmundsson, T. Sharma, T. Toulopoulou, T.D. Griffiths, A. Reveley and R. Murray

    Version of Record online : 12 SEP 2007, DOI: 10.1002/ajmg.b.30594

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    Experimental Dermatology

    Volume 25, Issue S2, February 2016, Pages: 1–13,

    Version of Record online : 19 FEB 2016, DOI: 10.1111/exd.12954

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    Clinicopathologic and genetic features of nonfamilial colorectal carcinomas with DNA replication errors


    Volume 82, Issue 2, 15 January 1998, Pages: 279–285, Shingo Senba, Fumio Konishi, Tomomi Okamoto, Hiroshi Kashiwagi, Kyotaro Kanazawa, Michiko Miyaki, Motoko Konishi and Toshihiko Tsukamoto

    Version of Record online : 31 OCT 2000, DOI: 10.1002/(SICI)1097-0142(19980115)82:2<279::AID-CNCR6>3.0.CO;2-M

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    Count of benign melanocytic nevi as a major indicator of risk for nonfamilial nodular and superficial spreading melanoma


    Volume 66, Issue 2, 15 July 1990, Pages: 387–395, J. J. Grob, J. Gouvernet, D. Aymar, A. Mostaque, M. H. Romano, A. M. Collet, M. C. Noe, M. P. Diconstanzo and J. J. Bonerandi

    Version of Record online : 28 JUN 2006, DOI: 10.1002/1097-0142(19900715)66:2<387::AID-CNCR2820660232>3.0.CO;2-J

  9. Genetic alterations on 3p, 11q13, and 18q in nonfamilial and MEN 1-associated pancreatic endocrine tumors

    Genes, Chromosomes and Cancer

    Volume 26, Issue 3, November 1999, Pages: 258–264, Ola Hessman, Daniel Lindberg, Annika Einarsson, Peter Lillhager, Tobias Carling, Lars Grimelius, Barbro Eriksson, Göran Åkerström, Gunnar Westin and Britt Skogseid

    Version of Record online : 28 SEP 1999, DOI: 10.1002/(SICI)1098-2264(199911)26:3<258::AID-GCC11>3.0.CO;2-2

  10. Frequent activation of the β-catenin-Tcf signaling pathway in nonfamilial colorectal carcinomas with microsatellite instability

    Genes, Chromosomes and Cancer

    Volume 30, Issue 1, January 2001, Pages: 32–37, Kazuhisa Shitoh, Taiji Furukawa, Masayuki Kojima, Fumio Konishi, Michiko Miyaki, Toshihiko Tsukamoto and Hideo Nagai

    Version of Record online : 23 OCT 2000, DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1065>3.0.CO;2-I

  11. Glomerular morphometry II: familial and nonfamilial haematuria


    Volume 5, Issue 3, May 1981, Pages: 251–256, N. YOSHIKAWA, A. H. CAMERON and R. H. R. WHITE

    Version of Record online : 3 APR 2007, DOI: 10.1111/j.1365-2559.1981.tb01783.x

  12. Familial and Nonfamilial Factors in the Prediction of Disruptive Behaviors in Boys at Risk for Substance Abuse

    Journal of Child Psychology and Psychiatry

    Volume 39, Issue 2, February 1998, Pages: 203–213, Partha P. Majumder, Howard B. Moss and Lenn Murrelle

    Version of Record online : 9 OCT 2003, DOI: 10.1111/1469-7610.00314

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    Familial carotid body tumors: Case report and epidemiologic review


    Volume 46, Issue 9, 1 November 1980, Pages: 2116–2122, Seymour Grufferman, Matthew W. Gillman, L. Reuven Pasternak, Caroline L. Peterson and W. Glenn Young Jr

    Version of Record online : 28 JUN 2006, DOI: 10.1002/1097-0142(19801101)46:9<2116::AID-CNCR2820460934>3.0.CO;2-S

  14. Two novel mutations of the NCSTN gene in Chinese familial acne inverse

    Journal of the European Academy of Dermatology and Venereology

    Volume 27, Issue 12, December 2013, Pages: 1571–1574, C. Zhang, L. Wang, L. Chen, W. Ren, A. Mei, X. Chen and Y. Deng

    Version of Record online : 3 JUL 2012, DOI: 10.1111/j.1468-3083.2012.04627.x

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    Expanding the spectrum of γ-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata

    Experimental Dermatology

    Volume 25, Issue 4, April 2016, Pages: 314–316, Uppala Ratnamala, Devendrasinh Jhala, Nayan K. Jain, Nazia M. Saiyed, Meda Raveendrababu, Mandava V. Rao, Timir Y. Mehta, Faiza M. Al-Ali, Kavi Raval, Sreelatha Nair, Nair K. Chandramohan, Murali R. Kuracha, Swapan K. Nath and Uppala Radhakrishna

    Version of Record online : 11 FEB 2016, DOI: 10.1111/exd.12911

  16. Hidradenitis suppurativa: haploinsufficiency of gamma-secretase components does not affect gamma-secretase enzyme activity in vitro

    British Journal of Dermatology

    Volume 175, Issue 3, September 2016, Pages: 632–635, A.E. Pink, D. Dafou, N. Desai, O. Holmes, C. Hobbs, C.H. Smith, P. Mortimer, M.A Simpson, R.C. Trembath and J.N. Barker

    Version of Record online : 28 JUL 2016, DOI: 10.1111/bjd.14621

  17. Recurrence of nonfamilial cardiac myxoma in the left ventricle: A case report

    Journal of Clinical Ultrasound

    Volume 42, Issue 9, November/December 2014, Pages: 576–577, Xiaole Song, Li Tang, Jun Yang and Nan Li

    Version of Record online : 4 MAY 2014, DOI: 10.1002/jcu.22168

  18. You have full text access to this OnlineOpen article
    Exome sequencing of three cases of familial exceptional longevity

    Aging Cell

    Volume 13, Issue 6, December 2014, Pages: 1087–1090, Timothy P. Cash, Guillermo Pita, Orlando Domínguez, Maria R. Alonso, Leticia T. Moreno, Consuelo Borrás, Leocadio Rodríguez-Mañas, Catalina Santiago, Nuria Garatachea, Alejandro Lucia, Juan A. Avellana, Jose Viña, Anna González-Neira and Manuel Serrano

    Version of Record online : 12 AUG 2014, DOI: 10.1111/acel.12261

  19. You Can't Always Get What You Want—Infant Care Preferences and Use Among Employed Mothers

    Journal of Marriage and Family

    Volume 64, Issue 1, February 2002, Pages: 2–15, Lisa A. Riley and Jennifer L. Glass

    Version of Record online : 2 MAR 2004, DOI: 10.1111/j.1741-3737.2002.00002.x

  20. The inheritance of alzheimer's disease: A new interpretation

    Annals of Neurology

    Volume 23, Issue 1, January 1988, Pages: 14–19, Dr. Naomi Fitch, Rubin Becker and Anita Heller

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410230104