D. Kedra

发表

Melanie E. Goward, Antony V. Cox, R. Durbin, 1999, Nature.

Third Report on Chicken Genes and Chromosomes 2015

Bronwen L. Aken, Hans H. Cheng, Andrew J. Oler, 2015, Cytogenetic and Genome Research.

Genome and transcriptome analysis of the Mesoamerican common bean and the role of gene duplications in establishing tissue and temporal specialization of genes

Juliane C. Dohm, R. Guigó, J. Dohm, 2016, Genome Biology.

The LZTFL1 gene is a part of a transcriptional map covering 250 kb within the common eliminated region 1 (C3CER1) in 3p21.3.

G. Klein, J. Dumanski, D. Kedra, 2001, Genomics.

The mouse ortholog of the human SMARCB1 gene encodes two splice forms.

C. Bruder, J. Dumanski, D. Kedra, 1999, Biochemical and biophysical research communications.

Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma

J. Dumanski, J. Coindre, J. Grosgeorge, 1997, Nature Genetics.

Role ofl-arginine, a substrate for nitric oxide-synthase, in gastroprotection and ulcer healing

D. Kedra, T. Brzozowski, S. Konturek, 1997, Journal of Gastroenterology.

Structure of the promoter and genomic organization of the human beta'-adaptin gene (BAM22) from chromosome 22q12.

B. Roe, S. Clifton, H. Pan, 1996, Genomics.

Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications

J. Dumanski, R. Płoski, D. Kedra, 2020, Molecular genetics & genomic medicine.

A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3

G. Klein, J. Dumanski, D. Kedra, 1999, Human Genetics.

Fine needle aspiration cytology combined with argyrophilic nucleolar organizer regions (AgNORs) in diagnosis of thyroid neoplasms.

D. Kedra, Z. Szybinski, K. Piotrowska, 1993, Endokrynologia Polska.

The germinal center kinase gene and a novel CDC25-like gene are located in the vicinity of the PYGM gene on 11q13

E. Blennow, J. Dumanski, D. Kedra, 1997, Human Genetics.

Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11.

J E Collins, B. Roe, I. Dunham, 1996, Human molecular genetics.

Characterization of the human synaptogyrin gene family

B. Roe, I. Dunham, H. Pan, 1998, Human Genetics.

ShiftDetector: detection of shift mutations

Eyal Seroussi, Micha Ron, Darek Kedra, 2002, Bioinform..

Fine mapping of the constitutional translocation t(11;22)(q23;q11)

B. Roe, E. Blennow, C. Bruder, 2000, Human Genetics.

Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma

C. Larsson, B. Teh, D. Kedra, 2001, Journal of medical genetics.

Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia

J. Dumanski, D. Kedra, S. Ivarsson, 2000, Human Genetics.

A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors.

G. Klein, J. Dumanski, D. Kedra, 1999, Genomics.

Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcripts.

B. Roe, P. Scambler, C. Schwartz, 1999, Genome research.

Haplotype selection as an adaptive mechanism in the protozoan pathogen Leishmania donovani

H. Himmelbauer, G. Bussotti, C. Notredame, 2017, Nature Ecology & Evolution.

Haplotype selection as an adaptive mechanism in the protozoan pathogen Leishmania donovani

H. Himmelbauer, G. Bussotti, C. Notredame, 2017, Nature Ecology & Evolution.

Protein identification and quantification by two-dimensional infrared spectroscopy: Implications for an all-optical proteomic platform

I. Gould, K. Willison, D. Klug, 2008, Proceedings of the National Academy of Sciences.

Characterization of the human NIPSNAP1 gene from 22q12: a member of a novel gene family.

B. Roe, H. Pan, J. Dumanski, 1998, Gene.

Sequence and Expression of the Mouse Homologue to Human Phospholipase C β3 Neighboring Gene

J. Dumanski, F. Piehl, D. Kedra, 1996 .

TOM1 genes map to human chromosome 22q13.1 and mouse chromosome 8C1 and encode proteins similar to the endosomal proteins HGS and STAM.

B. Roe, H. Pan, J. Dumanski, 1999, Genomics.

Correspondence re: P. P. Claudio et al., Mutations in the retinoblastoma-related gene RB2/p130 in primary nasopharyngeal carcinoma. Cancer Res., 60: 8-12, 2000.

B. Teh, D. Kedra, S. Gray, 2001, Cancer research.

Genomic structure, 5' flanking sequences, and precise localization in 1P31.1 of the human prostaglandin F receptor gene.

J. Dumanski, D. Kedra, R. Betz, 1999, Biochemical and biophysical research communications.