Gajecka M - Search Results

1

Gender Influences Gut Microbiota among Patients with Irritable Bowel Syndrome.

Pecyna P, Gabryel M, Mankowska-Wierzbicka D, Nowak-Malczewska DM, Jaskiewicz K, Jaworska MM, Tomczak H, Rydzanicz M, Ploski R, Grzymislawski M, Dobrowolska A, Gajecka M. Pecyna P, et al. Among authors: gajecka m. Int J Mol Sci. 2023 Jun 21;24(13):10424. doi: 10.3390/ijms241310424. Int J Mol Sci. 2023. PMID: 37445604 Free PMC article.

2

Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure.

Gajecka M, Yu W, Ballif BC, Glotzbach CD, Bailey KA, Shaw CA, Kashork CD, Heilstedt HA, Ansel DA, Theisen A, Rice R, Rice DP, Shaffer LG. Gajecka M, et al. Eur J Hum Genet. 2005 Feb;13(2):139-49. doi: 10.1038/sj.ejhg.5201302. Eur J Hum Genet. 2005. PMID: 15483646

3

Monosomy 1p36 deletion syndrome.

Gajecka M, Mackay KL, Shaffer LG. Gajecka M, et al. Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):346-56. doi: 10.1002/ajmg.c.30154. Am J Med Genet C Semin Med Genet. 2007. PMID: 17918734 Review.

4

Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.

D'Angelo CS, Gajecka M, Kim CA, Gentles AJ, Glotzbach CD, Shaffer LG, Koiffmann CP. D'Angelo CS, et al. Among authors: gajecka m. Hum Genet. 2009 Jun;125(5-6):551-63. doi: 10.1007/s00439-009-0650-9. Epub 2009 Mar 7. Hum Genet. 2009. PMID: 19271239

5

Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) gene.

Baris H, Bejjani BA, Tan WH, Coulter DL, Martin JA, Storm AL, Burton BK, Saitta SC, Gajecka M, Ballif BC, Irons MB, Shaffer LG, Kimonis VE. Baris H, et al. Among authors: gajecka m. Am J Med Genet A. 2006 Sep 1;140A(17):1876-9. doi: 10.1002/ajmg.a.31390. Am J Med Genet A. 2006. PMID: 16892302 No abstract available.

6

Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.

Gajecka M, Pavlicek A, Glotzbach CD, Ballif BC, Jarmuz M, Jurka J, Shaffer LG. Gajecka M, et al. Hum Genet. 2006 Nov;120(4):519-26. doi: 10.1007/s00439-006-0222-1. Epub 2006 Jul 18. Hum Genet. 2006. PMID: 16847692

7

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry CJ, McDonald-McGinn D, Medne L, Zackai E, Parsons J, Zand DJ, Hisama FM, Walsh CA, Leventer RJ, Martin CL, Gajecka M, Shaffer LG. Dobyns WB, et al. Among authors: gajecka m. Am J Med Genet A. 2008 Jul 1;146A(13):1637-54. doi: 10.1002/ajmg.a.32293. Am J Med Genet A. 2008. PMID: 18536050 Free PMC article.

8

[Significance of genetic factor in pathogenesis of laryngeal squamous cell carcinoma].

Gajecka M. Gajecka M. Otolaryngol Pol. 2003;57(1):139-40. Otolaryngol Pol. 2003. PMID: 12741160 Review. Polish. No abstract available.

9

Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.

Gajecka M, Glotzbach CD, Jarmuz M, Ballif BC, Shaffer LG. Gajecka M, et al. Eur J Hum Genet. 2006 Dec;14(12):1255-62. doi: 10.1038/sj.ejhg.5201710. Epub 2006 Aug 30. Eur J Hum Genet. 2006. PMID: 16941016

10

[Mutagen sensitivity in patients with multiple primary tumors (MPT) of the head and neck region--quantitative and qualitative assessment based on bleomycin assay].

Wierzbicka M, Jarmuz M, Gajecka M, Kujawski M, Szyfter W, Szyfter K. Wierzbicka M, et al. Among authors: gajecka m. Otolaryngol Pol. 2004;58(3):441-9. Otolaryngol Pol. 2004. PMID: 15311585 Polish.

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