Pollock NC - Search Results

1

KMT2D loss drives aggressive tumor phenotypes in cutaneous squamous cell carcinoma.

Dauch C, Shim S, Cole MW, Pollock NC, Beer AJ, Ramroop J, Klee V, Allain DC, Shakya R, Knoblaugh SE, Kulewsky J, Toland AE. Dauch C, et al. Among authors: pollock nc. Am J Cancer Res. 2022 Mar 15;12(3):1309-1322. eCollection 2022. Am J Cancer Res. 2022. PMID: 35411237 Free PMC article.

2

Differences in somatic TP53 mutation type in breast tumors by race and receptor status.

Pollock NC, Ramroop JR, Hampel H, Troester MA, Conway K, Hu JJ, Freudenheim JL, Olopade OI, Huo D, Ziv E, Neuhausen SL, Stevens P, McElroy JP, Toland AE. Pollock NC, et al. Breast Cancer Res Treat. 2022 Apr;192(3):639-648. doi: 10.1007/s10549-022-06509-3. Epub 2022 Mar 14. Breast Cancer Res Treat. 2022. PMID: 35286522 Free PMC article.

3

Effects of Tcte1 knockout on energy chain transportation and spermatogenesis: implications for male infertility.

Olszewska M, Malcher A, Stokowy T, Pollock N, Berman AJ, Budkiewicz S, Kamieniczna M, Jackowiak H, Suszynska-Zajczyk J, Jedrzejczak P, Yatsenko AN, Kurpisz M. Olszewska M, et al. Hum Reprod Open. 2024 Apr 4;2024(2):hoae020. doi: 10.1093/hropen/hoae020. eCollection 2024. Hum Reprod Open. 2024. PMID: 38650655 Free PMC article.

4

Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.

Tas E, Sebastian J, Madan-Khetarpal S, Sweet P, Yatsenko AN, Pollock N, Rajkovic A, Schneck FX, Yatsenko SA, Witchel SF. Tas E, et al. Am J Med Genet A. 2017 Jan;173(1):221-224. doi: 10.1002/ajmg.a.37981. Epub 2016 Sep 20. Am J Med Genet A. 2017. PMID: 27649277

5

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.

Khan MJ, Pollock N, Jiang H, Castro C, Nazli R, Ahmed J, Basit S, Rajkovic A, Yatsenko AN. Khan MJ, et al. Sci Rep. 2018 Nov 2;8(1):16280. doi: 10.1038/s41598-018-34262-5. Sci Rep. 2018. PMID: 30389958 Free PMC article.

6

A novel homozygous frame-shift variant in the LHCGR gene is associated with primary ovarian insufficiency in a Pakistani family.

Zielen AC, Khan MJ, Pollock N, Jiang H, Ahmed J, Nazli R, Jabeen M, Yatsenko A, Rajkovic A. Zielen AC, et al. Clin Genet. 2018 Oct;94(3-4):396-397. doi: 10.1111/cge.13406. Epub 2018 Jul 17. Clin Genet. 2018. PMID: 30016538 Free PMC article.

7

Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure.

Hardy JJ, Wyrwoll MJ, Mcfadden W, Malcher A, Rotte N, Pollock NC, Munyoki S, Veroli MV, Houston BJ, Xavier MJ, Kasak L, Punab M, Laan M, Kliesch S, Schlegel P, Jaffe T, Hwang K, Vukina J, Brieño-Enríquez MA, Orwig K, Yanowitz J, Buszczak M, Veltman JA, Oud M, Nagirnaja L, Olszewska M, O'Bryan MK, Conrad DF, Kurpisz M, Tüttelmann F, Yatsenko AN; GEMINI Consortium. Hardy JJ, et al. Among authors: pollock nc. Hum Genet. 2021 Aug;140(8):1169-1182. doi: 10.1007/s00439-021-02287-y. Epub 2021 May 7. Hum Genet. 2021. PMID: 33963445 Free PMC article.

8

Genomic testing for copy number and single nucleotide variants in spermatogenic failure.

Hardy J, Pollock N, Gingrich T, Sweet P, Ramesh A, Kuong J, Basar A, Jiang H, Hwang K, Vukina J, Jaffe T, Olszewska M, Kurpisz M, Yatsenko AN. Hardy J, et al. J Assist Reprod Genet. 2022 Sep;39(9):2103-2114. doi: 10.1007/s10815-022-02538-5. Epub 2022 Jul 18. J Assist Reprod Genet. 2022. PMID: 35849255 Free PMC article.

9

Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR): Molecular Cytogenetic Analysis.

Olszewska M, Stokowy T, Pollock N, Huleyuk N, Georgiadis A, Yatsenko S, Zastavna D, Yatsenko AN, Kurpisz M. Olszewska M, et al. Int J Mol Sci. 2020 Jun 26;21(12):4559. doi: 10.3390/ijms21124559. Int J Mol Sci. 2020. PMID: 32604929 Free PMC article.

10

Progress in childhood cancer care in Florida. 1970-1992.

Roush SW, Krischer JP, Cox MW, Bayer J, Pollock NC, Wilkinson AH Jr, Talbert JL. Roush SW, et al. Among authors: pollock nc. J Fla Med Assoc. 1993 Nov;80(11):747-51. J Fla Med Assoc. 1993. PMID: 8277234

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