Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

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Standort: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2041-1723

Umfang: Online-Ressource

Sprache: Englisch

Anmerkungen: online resource.

Erschienen in: Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment ; volume:9 ; number:1 ; day:17 ; month:5 ; year:2018 ; pages:1-14 ; date:12.2018
Nature Communications ; 9, Heft 1 (17.5.2018), 1-14, 12.2018

Urheber: Ashraf, Shazia

Beteiligte Personen und Organisationen: Kudo, Hiroki
Rao, Jia
Kikuchi, Atsuo
Widmeier, Eugen
Lawson, Jennifer A.
Tan, Weizhen
Hermle, Tobias Franz
Warejko, Jillian K.
Shril, Shirlee
Airik, Merlin
Jobst-Schwan, Tilman
Lovric, Svjetlana
Braun, Daniela A.
Gee, Heon Yung
Schapiro, David
Majmundar, Amar J.
Sadowski, Carolin E.
Pabst, Werner L.
Daga, Ankana
Ven, Amelie T. van der
Schmidt, Johanna M.
Low, Boon Chuan
Gupta, Anjali Bansal
Tripathi, Brajendra K.
Wong, Jenny
Campbell, Kirk
Metcalfe, Kay
Schanze, Denny
Niihori, Tetsuya
Kaito, Hiroshi
Nozu, Kandai
Tsukaguchi, Hiroyasu
Tanaka, Ryojiro
Hamahira, Kiyoshi
Kobayashi, Yasuko
Takizawa, Takumi
Funayama, Ryo
Nakayama, Keiko
Aoki, Yoko
Kumagai, Naonori
Iijima, Kazumoto
Fehrenbach, Henry
Kari, Jameela A.
El Desoky, Sherif
Jalalah, Sawsan
Bogdanovic, Radovan
Stajić, Nataša
Zappel, Hildegard
Rakhmetova, Assel
Wassmer, Sharon-Rose
Jungraithmayr, Therese
Strehlau, Jürgen
Kumar, Aravind Selvin
Bagga, Arvind
Soliman, Neveen A.
Mane, Shrikant M.
Kaufman, Lewis
Lowy, Douglas R.
Jairajpuri, Mohamad A.
Lifton, Richard P.
Pei, York
Zenker, Martin
Kure, Shigeo
Hildebrandt, Friedhelm
SpringerLink (Online service)

DOI: 10.1038/s41467-018-04193-w

URN: urn:nbn:de:101:1-2018071520400168882761

Rechteinformation: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Letzte Aktualisierung: 15.08.2025, 07:29 MESZ

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Beteiligte

Ashraf, Shazia
Kudo, Hiroki
Rao, Jia
Kikuchi, Atsuo
Widmeier, Eugen
Lawson, Jennifer A.
Tan, Weizhen
Hermle, Tobias Franz
Warejko, Jillian K.
Shril, Shirlee
Airik, Merlin
Jobst-Schwan, Tilman
Lovric, Svjetlana
Braun, Daniela A.
Gee, Heon Yung
Schapiro, David
Majmundar, Amar J.
Sadowski, Carolin E.
Pabst, Werner L.
Daga, Ankana
Ven, Amelie T. van der
Schmidt, Johanna M.
Low, Boon Chuan
Gupta, Anjali Bansal
Tripathi, Brajendra K.
Wong, Jenny
Campbell, Kirk
Metcalfe, Kay
Schanze, Denny
Niihori, Tetsuya
Kaito, Hiroshi
Nozu, Kandai
Tsukaguchi, Hiroyasu
Tanaka, Ryojiro
Hamahira, Kiyoshi
Kobayashi, Yasuko
Takizawa, Takumi
Funayama, Ryo
Nakayama, Keiko
Aoki, Yoko
Kumagai, Naonori
Iijima, Kazumoto
Fehrenbach, Henry
Kari, Jameela A.
El Desoky, Sherif
Jalalah, Sawsan
Bogdanovic, Radovan
Stajić, Nataša
Zappel, Hildegard
Rakhmetova, Assel
Wassmer, Sharon-Rose
Jungraithmayr, Therese
Strehlau, Jürgen
Kumar, Aravind Selvin
Bagga, Arvind
Soliman, Neveen A.
Mane, Shrikant M.
Kaufman, Lewis
Lowy, Douglas R.
Jairajpuri, Mohamad A.
Lifton, Richard P.
Pei, York
Zenker, Martin
Kure, Shigeo
Hildebrandt, Friedhelm
SpringerLink (Online service)

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Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

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Ähnliche Objekte (12)

HNPCC: Six new pathogenic mutations

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Phenotypic characterization of pathogenic mutations in GPIBDs

Protein destabilization underlies pathogenic missense mutations in ARID1B

Prioritization of pathogenic mutations in the protein kinase superfamily

Characterization of pathogenic germline mutations in human Protein Kinases

Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

Pathogenic mutations in UBQLN2 exhibit diverse aggregation propensity and neurotoxicity

Pathogenic mutations of human phosphorylation sites affect protein–protein interactions

Clinical challenges in interpreting multiple pathogenic mutations in single patients

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