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White Paper: Mimetics of Class 2 Tumor Suppressor Proteins as Novel Drug Candidates for Personalized Cancer Therapy

• Authors : Edgar Dahl; Sophia Villwock; Peter Habenberger

Subjects: tumor suppressor proteins; mimetics; personalized cancer therapy

• Source: Cancers; Volume 14; Issue 18; Pages: 4386

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White Paper: Mimetics of Class 2 Tumor Suppressor Proteins as Novel Drug Candidates for Personalized Cancer Therapy

• Authors : Edgar Dahl; Sophia Villwock; Peter Habenberger

Subjects: tumor suppressor proteins; mimetics; personalized cancer therapy

• Source: Cancers, Vol 14, Iss 4386, p 4386 (2022)

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Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing

• Authors : Allen, S; Balmaña, J; Domchek, S M

Subjects: Ataxia Telangiectasia Mutated Proteins/genetics; BRCA1 Protein/genetics; BRCA2 Protein/genetics

• Source: Allen , S , Balmaña , J , Domchek , S M , Evans , D G , Hoogerbrugge , N , Nathanson , K L , Tischkowitz , M , Foulkes , W D & Turnbull , C 2024 , ' Population-based germline breast cancer gene

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CTLA4 blockade abrogates KEAP1/STK11-related resistance to PD-(L)1 inhibitors.

• Authors : Skoulidis, Ferdinandos; Araujo, Haniel; Do, Minh

Subjects: Animals; Female; Humans

• Source: Nature: New biology, vol 635, iss 8038

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Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations

• Authors : Werren, Elizabeth A; Peirent, Emily R; Jantti, Henna ...

Subjects: Alleles; Cell Differentiation/genetics; Child

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The Impact of CREBRF rs373863828 Pacific-Variant on Infant Body Composition

• Authors : Amitrano, F; Krishnan, M; Murphy, R

Subjects: 3215 Reproductive Medicine; 32 Biomedical and Clinical Sciences; Clinical Trials and Supportive Activities

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BARD1 germline variants induce haploinsufficiency and DNA repair defects in neuroblastoma.

• Authors : Randall, Michael; Egolf, Laura; Vaksman, Zalman

Subjects: Humans; Tumor Suppressor Proteins; Genome-Wide Association Study

• Source: Journal of the National Cancer Institute, vol 116, iss 1

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Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.

• Authors : Kim, Jung; Vaksman, Zalman; Egolf, Laura

Subjects: Child; Humans; Genetic Predisposition to Disease

• Source: Journal of the National Cancer Institute, vol 116, iss 1

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Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.

• Authors : Panagiotakaki, Eleni; Tiziano, Francesco D; Mikati, Mohamad A ...

Subjects: Humans; Hemiplegia; Exome Sequencing

• Source: European journal of human genetics, Vol. 32, no.2, p. 224-231 (2024)

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Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.

• Authors : Panagiotakaki, Eleni; Tiziano, Francesco D; Mikati, Mohamad A ...

Subjects: Humans; Hemiplegia; Exome Sequencing

• Source: European journal of human genetics, Vol. 32, no.2, p. 224-231 (2024)

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