Loss-of-function mutations are main drivers of adaptations during short-term evolution

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Loss-of-function mutations are main drivers of adaptations during short-term evolution ; volume:14 ; number:1 ; day:26 ; month:3 ; year:2024 ; pages:1-8 ; date:12.2024
Scientific reports ; 14, Heft 1 (26.3.2024), 1-8, 12.2024

Creator: Klim, Joanna
Zielenkiewicz, Urszula
Kaczanowski, Szymon

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-024-57694-8

URN: urn:nbn:de:101:1-2406121219166.243825757652

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

Last update: 14.08.2025, 10:49 AM CEST

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Klim, Joanna
Zielenkiewicz, Urszula
Kaczanowski, Szymon
SpringerLink (Online service)

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Loss-of-function mutations are main drivers of adaptations during short-term evolution

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Other Objects (12)

Loss-of-function uORF mutations in human malignancies

Depletion of loss-of-function germline mutations in centenarians reveals longevity genes

Driver mutations of cancer epigenomes

Somatic evolutionary timings of driver mutations

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Loss-of-function myeloperoxidase mutations are associated with increased neutrophil counts and pustular skin disease

Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome

HotSpotter: efficient visualization of driver mutations

Sporadic multiple meningiomas harbor distinct driver mutations

Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis

Loss-of-function uORF mutations in human malignancies

Depletion of loss-of-function germline mutations in centenarians reveals longevity genes

Driver mutations of cancer epigenomes

Somatic evolutionary timings of driver mutations

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Loss-of-function myeloperoxidase mutations are associated with increased neutrophil counts and pustular skin disease

Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome

HotSpotter: efficient visualization of driver mutations

Sporadic multiple meningiomas harbor distinct driver mutations

Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis

Loss-of-function uORF mutations in human malignancies

Depletion of loss-of-function germline mutations in centenarians reveals longevity genes

Driver mutations of cancer epigenomes

Somatic evolutionary timings of driver mutations

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Loss-of-function myeloperoxidase mutations are associated with increased neutrophil counts and pustular skin disease

Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome

HotSpotter: efficient visualization of driver mutations

Sporadic multiple meningiomas harbor distinct driver mutations

Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis

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