Kaur K - Search Results

1

Broad spectrum identification of cellular small ubiquitin-related modifier (SUMO) substrate proteins.

Zhao Y, Kwon SW, Anselmo A, Kaur K, White MA. Zhao Y, et al. Among authors: kaur k. J Biol Chem. 2004 May 14;279(20):20999-1002. doi: 10.1074/jbc.M401541200. Epub 2004 Mar 11. J Biol Chem. 2004. PMID: 15016812 Free article.

2

Absence of cancer-associated changes in human fibroblasts immortalized with telomerase.

Morales CP, Holt SE, Ouellette M, Kaur KJ, Yan Y, Wilson KS, White MA, Wright WE, Shay JW. Morales CP, et al. Among authors: kaur kj. Nat Genet. 1999 Jan;21(1):115-8. doi: 10.1038/5063. Nat Genet. 1999. PMID: 9916803

3

Ral GTPases contribute to regulation of cyclin D1 through activation of NF-kappaB.

Henry DO, Moskalenko SA, Kaur KJ, Fu M, Pestell RG, Camonis JH, White MA. Henry DO, et al. Among authors: kaur kj. Mol Cell Biol. 2000 Nov;20(21):8084-92. doi: 10.1128/MCB.20.21.8084-8092.2000. Mol Cell Biol. 2000. PMID: 11027278 Free PMC article.

4

Isolation of effector-selective Ras mutants by yeast two-hybrid screening.

Kaur KJ, White MA. Kaur KJ, et al. Methods Enzymol. 2001;332:270-7. doi: 10.1016/s0076-6879(01)32209-7. Methods Enzymol. 2001. PMID: 11305103

5

RNA interference in mammalian cells by chemically-modified RNA.

Braasch DA, Jensen S, Liu Y, Kaur K, Arar K, White MA, Corey DR. Braasch DA, et al. Among authors: kaur k. Biochemistry. 2003 Jul 8;42(26):7967-75. doi: 10.1021/bi0343774. Biochemistry. 2003. PMID: 12834349

6

Disruption of the autism gene and chromatin regulator KDM5A alters hippocampal cell identity.

El Hayek L, DeVries D, Gogate A, Aiken A, Kaur K, Chahrour MH. El Hayek L, et al. Among authors: kaur k. Sci Adv. 2023 Nov 24;9(47):eadi0074. doi: 10.1126/sciadv.adi0074. Epub 2023 Nov 22. Sci Adv. 2023. PMID: 37992166 Free PMC article.

7

The genetic landscape of autism spectrum disorder in an ancestrally diverse cohort.

Gogate A, Kaur K, Khalil R, Bashtawi M, Morris MA, Goodspeed K, Evans P, Chahrour MH. Gogate A, et al. Among authors: kaur k. NPJ Genom Med. 2024 Dec 4;9(1):62. doi: 10.1038/s41525-024-00444-6. NPJ Genom Med. 2024. PMID: 39632905 Free PMC article.

8

Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants.

Tuncay IO, Parmalee NL, Khalil R, Kaur K, Kumar A, Jimale M, Howe JL, Goodspeed K, Evans P, Alzghoul L, Xing C, Scherer SW, Chahrour MH. Tuncay IO, et al. Among authors: kaur k. NPJ Genom Med. 2022 Feb 21;7(1):13. doi: 10.1038/s41525-022-00284-2. NPJ Genom Med. 2022. PMID: 35190550 Free PMC article.

9

Author Correction: The genetic landscape of autism spectrum disorder in an ancestrally diverse cohort.

Gogate A, Kaur K, Khalil R, Bashtawi M, Morris MA, Goodspeed K, Evans P, Chahrour MH. Gogate A, et al. Among authors: kaur k. NPJ Genom Med. 2024 Dec 26;9(1):72. doi: 10.1038/s41525-024-00458-0. NPJ Genom Med. 2024. PMID: 39725736 Free PMC article. No abstract available.

10

The ubiquitin ligase UBE3B, disrupted in intellectual disability and absent speech, regulates metabolic pathways by targeting BCKDK.

Cheon S, Kaur K, Nijem N, Tuncay IO, Kumar P, Dean M, Juusola J, Guillen-Sacoto MJ, Bedoukian E, Ierardi-Curto L, Kaplan P, Schaefer GB, Mishra P, Chahrour MH. Cheon S, et al. Among authors: kaur k. Proc Natl Acad Sci U S A. 2019 Feb 26;116(9):3662-3667. doi: 10.1073/pnas.1818751116. Epub 2019 Feb 11. Proc Natl Acad Sci U S A. 2019. PMID: 30808755 Free PMC article.

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