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  • 1-10 ل  108 نتائج ل ""DNA Helicases genetics""

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Academic Journal

Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra‐Cerebral Malformations

Subjects: Humans; Female; Pregnancy

  • Source: Prenatal diagnosis, vol. 44, no. 12, pp. 1526-1529

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Academic Journal

FANCM Gene Variants in a Male Diagnosed with Sertoli Cell-Only Syndrome and Diffuse Astrocytoma

Subjects: Male; Adult; 0303 health sciences

  • Source: Genes (Basel)

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Academic Journal

Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome

Subjects: Neuroinformatics; 0301 basic medicine; Heterozygote

  • Source: Genetics in Medicine, 24, 6, pp. 1283-1296Genetics in Medicine

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Academic Journal

Pan-cancer association of DNA repair deficiencies with whole-genome mutational patterns

Subjects: Male; DNA Repair; QH301-705.5

  • Source: eLifeeLife, Vol 12 (2023)Sørensen, S G, Shrikhande, A, Poulsgaard, G A, Christensen, M H, Bertl, J, Laursen, B E, Hoffmann, E R & Pedersen, J S 2023, ' Pan-cancer association of

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Academic Journal

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group

Subjects: Germline; Transcription Factors/genetics; SMARCB1

  • Source: Fam CancerFrühwald, M C, Nemes, K, Boztug, H, Cornips, M C A, Evans, D G, Farah, R, Glentis, S, Jorgensen, M, Katsibardi, K, Hirsch, S, Jahnukainen, K, Kventsel, I, Kerl, K, Kratz, C P,

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Academic Journal

Africa-specific human genetic variation near CHD1L associates with HIV-1 load.

Subjects: Humans; Cell Line; DNA Helicases/genetics

  • Source: Nature, vol. 620, no. 7976, pp. 1025-1030

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Academic Journal

Oct4 confers stemness and radioresistance to head and neck squamous cell carcinoma by regulating the homologous recombination factors PSMC3IP and RAD54L

Subjects: Aged [MeSH]; Octamer Transcription Factor-3/genetics [MeSH]; Neoplastic Stem Cells/pathology [MeSH]

  • Source: Oncogene

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Academic Journal

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

Subjects: Male; 0303 health sciences; Epilepsy

  • Source: Hum GenetHuman GeneticsHuman Genetics, 2021, Human Genetics, 140, pp.1109-1120.

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Academic Journal

CHD1 loss negatively influences metastasis-free survival in R0-resected prostate cancer patients and promotes spontaneous metastasis in vivo

Subjects: Male; Prostatectomy; 0303 health sciences

  • Source: Cancer Gene Ther

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Academic Journal

Simultaneous Brg1 Knockout and MYCN Overexpression in Cerebellar Granule Neuron Precursors Is Insufficient to Drive Tumor Formation but Temporarily Enhances their Proliferation and Delays their Migration

Subjects: Male; Mice, Knockout; N-Myc Proto-Oncogene Protein

  • Source: Cerebellum

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  • 1-10 ل  108 نتائج ل ""DNA Helicases genetics""