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Workshops - Fachschaftsinitiative Biomedizin
www.med.uni-wuerzburg.de
Organizer: Julia Doll / Michaela Hofrichter / Caroline Lekszas / Professor Dr. Thomas Haaf. Institute/Department: Institute of Human Genetics. Abstract: ...
Netzwerk-Profile
Caroline Lekszas - Speyer (Gymnasium am Kaiserdom)
www.stayfriends.de
Caroline Lekszas ist Mitglied bei StayFriends und hat bis diese Schule besucht: Gymnasium am Kaiserdom.
Caroline Lekszas | Semantic Scholar
www.semanticscholar.org
Semantic Scholar profile for Caroline Lekszas, with 1 highly influential citations and 9 scientific research papers.
Interessen
Bi-allelic variants in IPO8 cause a connective tissue ...Cell
www.cell.com
Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic. Martin, Frank Ruemmele, Dominique Bonneau, Nadine Cerf-Bensussan, Filippo Del.
lastFM: (CaroLekszas)
Alter: 25, weiblich
lastFM: CaroLekszas’s Music Profile | Last.fm
Caroline Lekszas, 25, FemaleLast seen: August plays since 29 Jul Loved Tracks | 0 Posts | 1 Playlist | 1 shout. Add as friend · Send a message ...
Business-Profile
Lenaers, Guy ( ; chercheur en biologie)IdRef
www.idref.fr
... Reza Maroofian, Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
Firmen-Mitarbeiter
Homa Tajsharghi - University of Skövde
www.his.se
Ariana Kariminejad, Emmanuelle Szenker-Ravi, Caroline Lekszas, Homa Tajsharghi, Ali-Reza Moslemi, Thomas Naert, Hong Thi Tran, ...
Mitarbeiter - Institut für Humangenetik
www.biozentrum.uni-wuerzburg.de
Lekszas Caroline, M.Sc. , AG Haaf, Liedtke Daniel, Dr. rer. nat. -wuerzburg.de, AG Klopocki ...
Bücher
Caroline Lekszas | University of Würzburg | 8 PublicationsTypeset
typeset.io
Caroline Lekszas is an academic researcher from University of Würzburg. The author has contributed to research in topic(s): Endoplasmic reticulum ...
Erweiterung des genetischen Mutationsspektrums verschiedenerGoogle
books.google.com
Caroline Lekszas. Julius-Maximilians-Universität Würzburg, Reviews. Reviews aren't verified, but Google checks for and removes fake content when ...
Aboulfazl RadResearchpad.co
www.researchpad.co
... Reza Maroofian, Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
Homozygous null TBX4 mutations lead to posterior amelia with pelvic...
biblio.ugent.be
Kariminejad, Ariana, Emmanuelle Szenker-Ravi, Caroline Lekszas, Homa Tajsharghi, Ali-Reza Moslemi, Thomas Naert, Hong Tran Thi, et al.
Dokumente zum Namen
Proteomic Analysis of Restored Insulin Production and ...American Chemical Society
pubs.acs.org
von T Kang · · Zitiert von: 19 — The EMBO Journal 2020, 39 (10) https://doi.org embj ; Caroline Lekszas, Ombretta Foresti, Ishier Raote, Daniel Liedtke, ...
A new patella syndrome - Sandhaus John Wiley
onlinelibrary.wiley.com
von YS Sandhaus · · Zitiert von: 16 — Ariana Kariminejad, Emmanuelle Szenker-Ravi, Caroline Lekszas, Homa Tajsharghi, Ali-Reza Moslemi, Thomas Naert, Hong Thi Tran, Fatemeh Ahangari, ...
A biallelic variant in CLRN2 causes non-syndromic hearing ...University College London
discovery.ucl.ac.uk
von B Vona · · Zitiert von: 14 — Caroline Lekszas, Dr. Daniel. Liedtke, and Dr. Indrajit Nanda from the Institute of Human Genet- ics at the University of Würzburg for their technical expertise ...
Biallelic TANGO1 mutations cause a novel syndromal ...ProQuest
search.proquest.com
von L Caroline · · Zitiert von: 40 — Caroline Lekszas, Validation, Investigation, Visualization, Methodology, Writing - original draft;. Ombretta Foresti, Validation, Investigation, ...
Wissenschaftliche Veröffentlichungen
Homozygous Null TBX4 Mutations Lead to Posterior ...ScienceDirect
www.sciencedirect.com
von A Kariminejad · · Zitiert von: 17 — Author links open overlay panel. Ariana Kariminejad , Emmanuelle Szenker-Ravi , Caroline Lekszas , Homa Tajsharghi 4
Promotionskolloquium Caroline Lekszas; Fakultät für ...Universität Würzburg
www.biozentrum.uni-wuerzburg.de
Ort: Hubland Nord, Geb. 21, ; Veranstalter: Fakultät für Biologie, via Zoom ; Vortragende*r: Caroline Lekszas; M. Sc. Lekszas Caroline (Dr.) Vertreten in. Institut für Humangenetik Telefon + Visitenkarte Download.
Veröffentlichungen allgemein
Nature Communications - EconPapersRePEc
econpapers.repec.org
... Albertien M. Eerde, Koen L. Gassen, Corstiaan C. Breugem, Alexander Stegmann, Caroline Lekszas, Reza Maroofian, Ehsan Ghayoor Karimiani, Arnaud Bruneel, ...
Trisomy 4p due to a paternal t(4p-;16p+) translocationSpringer
link.springer.com
von T Bauknecht · · Zitiert von: 15 — ... t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report. 07 June Caroline Lekszas, Indrajit Nanda, …
(PDF) Unbalanced Segregation of a PaternalAmanote
research.amanote.com
— Caroline Lekszas Indrajit Nanda Barbara Vona Julia Böck Farah Ashrafzadeh Nahid Donyadideh Farnoosh Ebrahimzadeh Najmeh Ahangari Reza ...
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4)...
link.springer.com
4) translocation causing familial Beckwith-Wiedemann syndrome: a case report. Caroline Lekszas ,; Indrajit Nanda , ...
Artikel & Meinungen
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis...
www.nature.com
Caroline Lekszas. Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, Cranmer Terrace, ...
Sonstiges
Caroline Lekszas's research works | University of ...ResearchGate
www.researchgate.net
Caroline Lekszas's 11 research works with 112 citations and reads, including: A biallelic gain-of-function variant in MSGN1 causes a new skeletal ...
Bi-allelic variants in IPO8 cause a connective tissue ...National Institutes of Health (.gov)
www.ncbi.nlm.nih.gov
von A Ziegler · · Zitiert von: 11 — ... Maroofian,27 Aboulfazl Rad,28 Barbara Vona,28,29 Ehsan Ghayoor Karimiani,30,31Caroline Lekszas,29 Thomas Haaf,29 Ludovic Martin,2,32 Frank Ruemmele,3, von C Lekszas · · Zitiert von: 40 — Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion. Caroline Lekszas,#1,‡ Ombretta Foresti,#2, ...
Bi-allelic variants in IPO8 cause a connective tissue disorder ...Inrae
hal.inrae.fr
... Ehsan Ghayoor Karimiani (23) , Caroline Lekszas (24) , Thomas Haaf (24) , Ludovic Martin (2, 1) , Frank Ruemmele (5, 11) , Dominique Bonneau (1, ...
Bi-allelic variants in IPO8 cause a connective tissue disorder ...elsevierpure.com
squ.elsevierpure.com
von A Ziegler · · Zitiert von: 11 — ... Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
Biallelic TANGO1 mutations cause a novel CiNii Research国立情報学研究所
cir.nii.ac.jp
Caroline Lekszas: Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany. Ombretta Foresti: Centre for Genomic Regulation, ...
Citation Search ResultsMirus Bio LLC
www.mirusbio.com
Caroline Lekszas, Ombretta Foresti, Ishier Raote, et al. Journal bioRxiv (2019) n/a: Product Usage Product: TransIT®-293 Transfection Reagent
Dr. Vivek Malhotra, MD – Akron, OH | PediatricsDoximity
www.doximity.com
Caroline Lekszas, Ombretta Foresti, Ishier Raote, Daniel Liedtke, Eva-Maria König, Indrajit Nanda, Barbara Vona, Peter De Coster, Rita Cauwels, ...
Dual Diagnosis of Ellis-van Creveld Syndrome and ...Karger Publishers
karger.com
von B Vona · · Zitiert von: 10 — Caroline Lekszas;. Caroline Lekszas. aInstitute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany; ...
Emedgene ResearchEmedgene
www.emedgene.com
... Reza Maroofian, Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
Homa Tajsharghi - Högskolan i Skövdehis.se
www.his.se
Ariana Kariminejad, Emmanuelle Szenker-Ravi, Caroline Lekszas, Homa Tajsharghi, Ali-Reza Moslemi, Thomas Naert, Hong Thi Tran, Fatemeh Ahangari, ...
Homozygous Null TBX4 Mutations Lead to Posterior ...Europe PMC
europepmc.org
von A Kariminejad · · Zitiert von: 17 — Ariana Kariminejad,1,15,16 Emmanuelle Szenker-Ravi,2,15Caroline Lekszas,3,15 Homa Tajsharghi,4 Ali-Reza Moslemi,5 Thomas Naert,6 Hong Thi Tran,6 Fatemeh ...
Hong Tran Thi | Research Portalresearchportal.be
researchportal.be
Authors: Ariana Kariminejad, Emmanuelle Szenker-Ravi, Caroline Lekszas, Homa Tajsharghi, Ali-Reza Moslemi, Thomas Naert, Hong Tran Thi, Fatemeh Ahangari, ...
LUCIE MARTINInstitut Curie
curie.fr
... Reza Maroofian, Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
LUCIE MARTINInstitut-curie.org
institut-curie.org
... Reza Maroofian, Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
Najmeh AHANGARI - 中国教育图书进出口有限公司socolar.com
www.socolar.com
16条结果 — 作者：Caroline Lekszas ;Indrajit Nanda ;Barbara Vona 等. 来源：BMC Medical Genomics ;12(1):1-7.doi: s y.
OdontochondrodysplasiaMedChemExpress
www.medchemexpress.com
Odontochondrodysplasia · [1]. Anika Wehrle, et al. Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. · [2]. Caroline Lekszas, et al. Biallelic TANGO1 ...
Putting JNK1 on the immunodeficiency mapResearcher App
www.researcher-app.com
... Reza Maroofian, Aboulfazl Rad, Barbara Vona, Ehsan Ghayoor Karimiani, Caroline Lekszas, Thomas Haaf, Ludovic Martin, Frank Ruemmele, Dominique Bonneau, ...
Request a detailed protocolBio-protocol
bio-protocol.org
Short report. Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion. Caroline Lekszas et al.
SLC10A7 mutations cause a skeletal dysplasia with ...Maastricht University
cris.maastrichtuniversity.nl
von J Dubail · · Zitiert von: 34 — ... Koen L. van Gassen, Corstiaan C. Breugem, Alexander Stegmann, Caroline Lekszas, Reza Maroofian, Ehsan Ghayoor Karimiani, Arnaud Bruneel, ...
SLC10A7 mutations cause a skeletal dysplasia with ...Sorbonne Université
hal.sorbonne-universite.fr
von J Dubail · · Zitiert von: 34 — Caroline Lekszas (16) , Reza Maroofian (17) , Ehsan Ghayoor Karimiani (17, 18, 19) , Arnaud Bruneel (20) , Nathalie Seta
Verwandte Suchanfragen zu Caroline Lekszas
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