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2024
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Sacherschließung
Mutation, Missense [MeSH]
(9)
Humans [MeSH]
(8)
Male [MeSH]
(7)
Female [MeSH]
(5)
Child [MeSH]
(4)
article
(2)
Transcription Factors/genetics [MeSH]
(2)
Original Investigation
(2)
Child, Preschool [MeSH]
(2)
Article
(2)
Publikationstyp
Artikel
(9)
Medium
Erscheinungsjahr
Institution
9 Treffer
Kurzansicht
E-Jahr
Zugriff
Typ
Operations
Unraveling novel mutation patterns and morphological variations in two dalbavancin-resistant MRSA strains in Austria using whole genome sequencing and transmission electron microscopy
2024 .
Hotz, Julian Frederic
|
Staudacher, Moritz
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Schefberger, Katharina
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Spettel, Kathrin
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Schmid, Katharina
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Kriz, Richard
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Schneider, Lisa
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Hagemann, Jürgen Benjamin
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Cyran, Norbert
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Schmidt, Katy
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Starzengruber, Peter
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Lötsch, Felix
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Leutzendorff, Amelie
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Daller, Simon
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Ramharter, Michael
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Burgmann, Heinz
|
Lagler, Heimo
2024
http://purl.org/ontology/bibo/Article
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles
2024 .
Bassani, Sissy
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Chrast, Jacqueline
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Ambrosini, Giovanna
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Voisin, Norine
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Schütz, Frédéric
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Brusco, Alfredo
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Sirchia, Fabio
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Turban, Lydia
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Schubert, Susanna
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Abou Jamra, Rami
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Schlump, Jan-Ulrich
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DeMille, Desiree
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Bayrak-Toydemir, Pinar
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Nelson, Gary Rex
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Wong, Kristen Nicole
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Duncan, Laura
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Mosera, Mackenzie
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Gilissen, Christian
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Vissers, Lisenka E. L. M.
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Pfundt, Rolph
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Kersseboom, Rogier
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Yttervik, Hilde
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Hansen, Geir Åsmund Myge
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Smeland, Marie Falkenberg
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Butler, Kameryn M.
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Lyons, Michael J.
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Carvalho, Claudia M. B.
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Zhang, Chaofan
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Lupski, James R.
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Potocki, Lorraine
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Flores-Gallegos, Leticia
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Morales-Toquero, Rodrigo
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Petit, Florence
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Yalcin, Binnaz
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Tuttle, Annabelle
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Elloumi, Houda Zghal
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McCormick, Lane
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Kukolich, Mary
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Klaas, Oliver
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Horvath, Judit
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Scala, Marcello
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Iacomino, Michele
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Operto, Francesca
|
Zara, Federico
|
Writzl, Karin
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Maver, Aleš
|
Haanpää, Maria K.
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Pohjola, Pia
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Arikka, Harri
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Kievit, Anneke J. A.
|
Calandrini, Camilla
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Iseli, Christian
|
Guex, Nicolas
|
Reymond, Alexandre
2024
http://purl.org/ontology/bibo/Article
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss
2024 .
Redfield , Shelby
|
De-la-Torre, Pedro
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Zamani, Mina
|
Wang, Hanjun
|
Khan, Hina
|
Morris, Tyler
|
Shariati, Gholamreza
|
Karimi, Majid
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Kenna, Margaret
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Seo, Go Hun
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Xu, Hongen
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Lu, Wei
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Naz, Sadaf
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Galehdari, Hamid
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Indzhykulian, Artur
|
Shearer, Aiden
|
Vona, Barbara
2024
http://purl.org/ontology/bibo/Article
Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes
2024 .
Schmidt, Julia
|
Kaulfuß, Silke
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Ott, Hagen
|
Gaubert, Marianne
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Reintjes, Nadine
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Bremmer, Felix
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Dreha-Kulaczewski, Steffi
|
Stroebel, Philipp
|
Yigit, Gökhan
|
Wollnik, Bernd
2024
http://purl.org/ontology/bibo/Article
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract
2024 .
Kesdiren, Esra
|
Martens, Helge
|
Brand, Frank
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Werfel, Lina
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Wedekind, Lukas
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Trowe, Mark-Oliver
|
Schmitz, Jessica
|
Hennies, Imke
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Geffers, Robert
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Gucev, Zoran
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Seeman, Tomáš
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Schmidt, Sonja
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Tasic, Velibor
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Fasano, Laurent
|
Bräsen, Jan H.
|
Kispert, Andreas
|
Christians, Anne
|
Haffner, Dieter
|
Weber, Ruthild
2024
http://purl.org/ontology/bibo/Article
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy
2024 .
Sajan, Samin A.
|
Gradisch, Ralph
|
Vogel, Florian D.
|
Coffey, Alison
|
Salyakina, Daria
|
Soler, Diana
|
Jayakar, Parul
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Jayakar, Anuj
|
Bianconi, Simona E.
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Cooper, Annina H.
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Liu, Shuxi
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William, Nancy
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Benkel-Herrenbrück, Ira
|
Maiwald, Robert
|
Heller, Corina
|
Biskup, Saskia
|
Leiz, Steffen
|
Westphal, Dominik Sebastian
|
Wagner, Matias
|
Clarke, Amy
|
Stockner, Thomas
|
Ernst, Margot
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Kesari, Akanchha
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Krenn, Martin
2024
http://purl.org/ontology/bibo/Article
Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy
2024 .
Kopp, Johannes
|
Koch, Leonard
|
Lyubenova, Hristiana
|
Küchler, Oliver
|
Holtgrewe, Manuel
|
Ivanov, Andranik
|
Dubourg, Christele
|
L, Erika
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Brachs, Sebastian
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Mundlos, Stefan
|
Ehmke, Nadja
|
Seelow, Dominik
|
fradin, melanie
|
Kornak, Uwe
|
Fischer-Zirnsak, Björn
2024
http://purl.org/ontology/bibo/Article
Different growth patterns in two siblings with Schimke immuno-osseous-dysplasia
2024 .
Bokenkamp, Arend
|
Bouts, Antonia
|
van der Weerd, Neeltje
|
Levtchenko, Elena
|
Haffner, Dieter
|
Zivicnjak, Miroslav
2024
http://purl.org/ontology/bibo/Article
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly
2024 .
Herbst, Charlotte
|
Bothe, Viktoria
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Wegler, Meret
|
Axer-Schaefer, Susanne
|
Audebert-Bellanger, Séverine
|
Gecz, Jozef
|
Cogne, Benjamin
|
Feldman, Hagit Baris
|
Horn, Anselm H. C.
|
Hurst, Anna C. E.
|
Kelly, Melissa A.
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Kruer, Michael C.
|
Kurolap, Alina
|
Laquerriere, Annie
|
Li, Megan
|
Mark, Paul R.
|
Morawski, Markus
|
Nizon, Mathilde
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Pastinen, Tomi
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Polster, Tilman
|
Saugier-Veber, Pascale
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SeSong, Jang
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Sticht, Heinrich
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Stieler, Jens T.
|
Thifffault, Isabelle
|
van Eyk, Clare L.
|
Marcorelles, Pascale
|
Vezain-Mouchard, Myriam
|
Abou Jamra, Rami
|
Oppermann, Henry
2024
http://purl.org/ontology/bibo/Article