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There are 26183 results for: content related to: A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia

  1. ALDH1A1 is a Marker of Astrocytic Differentiation during Brain Development and Correlates with Better Survival in Glioblastoma Patients

    Brain Pathology

    Volume 22, Issue 6, November 2012, Pages: 788–797, S. Alexandra Adam, Oliver Schnell, Julia Pöschl, Sabina Eigenbrod, Hans A. Kretzschmar, Jörg-Christian Tonn and Ulrich Schüller

    Version of Record online : 19 APR 2012, DOI: 10.1111/j.1750-3639.2012.00592.x

  2. You have free access to this content
    Mutations in ALDH1A3 cause microphthalmia

    Clinical Genetics

    Volume 84, Issue 2, August 2013, Pages: 128–131, M A Aldahmesh, A O Khan, H Hijazi and F S Alkuraya

    Version of Record online : 27 MAY 2013, DOI: 10.1111/cge.12184

  3. You have free access to this content
    New sources of retinoic acid synthesis revealed by live imaging of an Aldh1a2-GFP reporter fusion protein throughout zebrafish development

    Developmental Dynamics

    Volume 241, Issue 7, July 2012, Pages: 1205–1216, Silke Pittlik and Gerrit Begemann

    Version of Record online : 29 MAY 2012, DOI: 10.1002/dvdy.23805

  4. Aberrant expression of aldehyde dehydrogenase 1A (ALDH1A) subfamily genes in acute lymphoblastic leukaemia is a common feature of T-lineage tumours

    British Journal of Haematology

    Volume 168, Issue 2, January 2015, Pages: 246–257, Brooke A. C. Longville, Denise Anderson, Mathew D. Welch, Ursula R. Kees and Wayne K. Greene

    Version of Record online : 11 SEP 2014, DOI: 10.1111/bjh.13120

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    Late Aptian (Cretaceous) paleoceanography of the South Atlantic Ocean inferred from dinocyst communities of the Sergipe Basin, Brazil


    Volume 31, Issue 1, January 2016, Pages: 2–26, Marcelo de A. Carvalho, Peter Bengtson and Cecília C. Lana

    Version of Record online : 9 JAN 2016, DOI: 10.1002/2014PA002772

  6. Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

    Clinical Genetics

    Volume 86, Issue 4, October 2014, Pages: 326–334, N. Chassaing, A. Causse, A. Vigouroux, A. Delahaye, J.-L. Alessandri, O. Boespflug-Tanguy, O. Boute-Benejean, H. Dollfus, B. Duban-Bedu, B. Gilbert-Dussardier, F. Giuliano, M. Gonzales, M. Holder-Espinasse, B. Isidor, M.-L. Jacquemont, D. Lacombe, D. Martin-Coignard, M. Mathieu-Dramard, S. Odent, O. Picone, L. Pinson, C. Quelin, S. Sigaudy, A. Toutain, C. Thauvin-Robinet, Josseline Kaplan and Patrick Calvas

    Version of Record online : 7 OCT 2013, DOI: 10.1111/cge.12275

  7. Throwing caution to the wind: The effect of CEO stock option pay on the incidence of product safety problems

    Strategic Management Journal

    Volume 36, Issue 7, July 2015, Pages: 1082–1092, Adam J. Wowak, Michael J. Mannor and Kaitlin D. Wowak

    Version of Record online : 2 JUL 2014, DOI: 10.1002/smj.2277

  8. Retrospective study of the medium-chain acyl-CoA dehydrogenase deficiency in Portugal

    Clinical Genetics

    Volume 85, Issue 6, June 2014, Pages: 555–561, F.V. Ventura, P. Leandro, A. Luz, I.A. Rivera, M.F.B. Silva, R. Ramos, H. Rocha, A. Lopes, H. Fonseca, A. Gaspar, L. Diogo, E. Martins, E. Leão-Teles, L. Vilarinho and I. Tavares de Almeida

    Version of Record online : 28 JUL 2013, DOI: 10.1111/cge.12227


    Economic Inquiry

    Volume 54, Issue 2, April 2016, Pages: 1319–1338, Yuqing Zheng and Harry M. Kaiser

    Version of Record online : 12 OCT 2015, DOI: 10.1111/ecin.12277

  10. Occupational contact dermatitis in blue-collar workers: results from a multicentre study from the Danish Contact Dermatitis Group (2003–2012)

    Contact Dermatitis

    Volume 71, Issue 6, December 2014, Pages: 348–355, Jakob F. Schwensen, Torkil Menné, Niels K. Veien, Anne T. Funding, Christian Avnstorp, Morten Østerballe, Klaus E. Andersen, Evy Paulsen, Charlotte G. Mørtz, Mette Sommerlund, Anne Danielsen, Bo L. Andersen, Jens Thormann, Ove Kristensen, Berit Kristensen, Susanne Vissing, Niels H. Nielsen, Jacob P. Thyssen and Jeanne D. Johansen

    Version of Record online : 18 JUL 2014, DOI: 10.1111/cod.12277

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    Erratum: Erratum

    Vol. 73, Issue 1, 67, Version of Record online: 8 JUN 2015

  11. Decomposition kinetics and organic geochemistry of woody debris in a ferralsol in a humid tropical climate

    European Journal of Soil Science

    Volume 66, Issue 5, September 2015, Pages: 876–885, K. Fujisaki, A.-S. Perrin, M. Boussafir, S. Gogo, M. Sarrazin and M. Brossard

    Version of Record online : 25 JUN 2015, DOI: 10.1111/ejss.12277

  12. Role of selective peroxisome proliferator-activated receptor modulators in managing cardiometabolic disease: tale of a roller-coaster

    Diabetes, Obesity and Metabolism

    Volume 16, Issue 9, September 2014, Pages: 780–792, A. Sahebkar and G. F. Watts

    Version of Record online : 11 MAR 2014, DOI: 10.1111/dom.12277

  13. Value of MRI olfactory bulb evaluation in the assessment of olfactory dysfunction in Bardet–Biedl syndrome

    Clinical Genetics

    Volume 90, Issue 1, July 2016, Pages: 79–83, J.J. Braun, V. Noblet, S. Kremer, S. Molière, H. Dollfus, V. Marion, N. Goetz, J. Muller and S. Riehm

    Version of Record online : 8 JAN 2016, DOI: 10.1111/cge.12697

  14. MicroRNA-200c attenuates tumour growth and metastasis of presumptive head and neck squamous cell carcinoma stem cells

    The Journal of Pathology

    Volume 223, Issue 4, March 2011, Pages: 482–495, Wen-Liang Lo, Cheng-Chia Yu, Guang-Yuh Chiou, Yi-Wei Chen, Pin-I Huang, Chian-Shiu Chien, Ling-Ming Tseng, Pen-Yuan Chu, Kai-Hsi Lu, Kuo-Wei Chang, Shou-Yen Kao and Shih-Hwa Chiou

    Version of Record online : 5 JAN 2011, DOI: 10.1002/path.2826

  15. Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing

    Clinical Genetics

    Volume 88, Issue 5, November 2015, Pages: 441–449, R.J. Pengelly, R. Upstill-Goddard, L. Arias, J. Martinez, J. Gibson, M. Knut, A.L. Collins, S. Ennis, A. Collins and I. Briceno

    Version of Record online : 6 JAN 2015, DOI: 10.1111/cge.12547

  16. Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders

    Clinical Genetics

    Volume 87, Issue 5, May 2015, Pages: 430–439, A. Chaussenot, C. Rouzier, M. Quere, M. Plutino, S. Ait-El-Mkadem, S. Bannwarth, M. Barth, H. Dollfus, P. Charles, M. Nicolino, B. Chabrol, B. Vialettes and V. Paquis-Flucklinger

    Version of Record online : 6 AUG 2014, DOI: 10.1111/cge.12437

  17. Clinical and descriptive genetic study of polydactyly: a Pakistani experience of 313 cases

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 482–486, S. Malik, S. Ullah, M. Afzal, K. Lal and S. Haque

    Version of Record online : 5 JUL 2013, DOI: 10.1111/cge.12217

  18. Is retinoic acid genetic machinery a chordate innovation?

    Evolution & Development

    Volume 8, Issue 5, September/October 2006, Pages: 394–406, Cristian Cañestro, John H. Postlethwait, Roser Gonzàlez-Duarte and Ricard Albalat

    Version of Record online : 22 AUG 2006, DOI: 10.1111/j.1525-142X.2006.00113.x

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    A systematic approach to assessing the clinical significance of genetic variants

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 453–463, H Duzkale, J Shen, H McLaughlin, A Alfares, MA Kelly, TJ Pugh, BH Funke, HL Rehm and MS Lebo

    Version of Record online : 17 OCT 2013, DOI: 10.1111/cge.12257

  20. A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands

    Clinical Genetics

    Volume 85, Issue 4, April 2014, Pages: 318–327, R. van Minkelen, Y. van Bever, J.N.R. Kromosoeto, C.J. Withagen-Hermans, A. Nieuwlaat, D.J.J. Halley and A.M.W. van den Ouweland

    Version of Record online : 25 JUN 2013, DOI: 10.1111/cge.12187