Chemoproteogenomic stratification of the missense variant cysteinome

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Chemoproteogenomic stratification of the missense variant cysteinome ; volume:15 ; number:1 ; day:28 ; month:10 ; year:2024 ; pages:1-24 ; date:12.2024
Nature Communications ; 15, Heft 1 (28.10.2024), 1-24, 12.2024

Creator: Desai, Heta
Andrews, Katrina H.
Bergersen, Kristina V.
Ofori, Samuel
Yu, Fengchao
Shikwana, Flowreen
Arbing, Mark A.
Boatner, Lisa M.
Villanueva, Miranda
Ung, Nicholas
Reed, Elaine F.
Nesvizhskii, Alexey I.
Backus, Keriann M.

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41467-024-53520-x

URN: urn:nbn:de:101:1-2501172134296.605299217591

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:34 AM CEST

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Desai, Heta
Andrews, Katrina H.
Bergersen, Kristina V.
Ofori, Samuel
Yu, Fengchao
Shikwana, Flowreen
Arbing, Mark A.
Boatner, Lisa M.
Villanueva, Miranda
Ung, Nicholas
Reed, Elaine F.
Nesvizhskii, Alexey I.
Backus, Keriann M.
SpringerLink (Online service)

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Chemoproteogenomic stratification of the missense variant cysteinome

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Other Objects (12)

Missense variant contribution to USP9X-female syndrome

The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density

Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant

Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy

KIF15 missense variant is associated with the early onset of idiopathic pulmonary fibrosis

Heterozygous missense variant in GLI2 impairs human endocrine pancreas development

SOAT1 missense variant in two cats with sebaceous gland dysplasia

A dominant missense variant within LMBR1 related to equine polydactyly

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes

A missense variant in the nuclear localization signal of DKC1 causes Hoyeraal-Hreidarsson syndrome

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

A rare missense variant in NR1H4 associates with lower cholesterol levels

Missense variant contribution to USP9X-female syndrome

The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density

Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant

Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy

KIF15 missense variant is associated with the early onset of idiopathic pulmonary fibrosis

Heterozygous missense variant in GLI2 impairs human endocrine pancreas development

SOAT1 missense variant in two cats with sebaceous gland dysplasia

A dominant missense variant within LMBR1 related to equine polydactyly

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes

A missense variant in the nuclear localization signal of DKC1 causes Hoyeraal-Hreidarsson syndrome

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

A rare missense variant in NR1H4 associates with lower cholesterol levels

Missense variant contribution to USP9X-female syndrome

The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density

Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant

Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy

KIF15 missense variant is associated with the early onset of idiopathic pulmonary fibrosis

Heterozygous missense variant in GLI2 impairs human endocrine pancreas development

SOAT1 missense variant in two cats with sebaceous gland dysplasia

A dominant missense variant within LMBR1 related to equine polydactyly

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes

A missense variant in the nuclear localization signal of DKC1 causes Hoyeraal-Hreidarsson syndrome

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

A rare missense variant in NR1H4 associates with lower cholesterol levels

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