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BMC Genomics
|
August 25, 2022
Revised time estimation of the ancestral human chromosome 2 fusion
Barbara Poszewiecka, Krzysztof Gogolewski, Paweł Stankiewicz, et al.
Respiratory Research
|
January 22, 2021
Potential interactions between the TBX4-FGF10 and SHH-FOXF1 signaling during human lung development revealed using ChIP-seq
Justyna A Karolak, Tomasz Gambin, Przemyslaw Szafranski, et al.
Prenatal Diagnosis
|
April 8, 2022
Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges
Roni Zemet, Ignatia B Van den Veyver, Paweł Stankiewicz
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
November 21, 2013
Chromosome conformation capture-on-chip analysis of long-range cis-interactions of the SOX9 promoter
Marta Smyk, Przemyslaw Szafranski, Michał Startek, et al.
American Journal of Medical Genetics. Part A
|
June 11, 2015
A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures
Marta Smyk, Elizabeth Roeder, Sau Wai Cheung, et al.
Human Mutation
|
March 19, 2021
Lung-specific distant enhancer cis regulates expression of FOXF1 and lncRNA FENDRR
Przemyslaw Szafranski, Tomasz Gambin, Justyna A Karolak, et al.
Genome Biology
|
September 12, 2023
PhaseDancer: a novel targeted assembler of segmental duplications unravels the complexity of the human chromosome 2 fusion going from 48 to 46 chromosomes in hominin evolution
Barbara Poszewiecka, Krzysztof Gogolewski, Justyna A Karolak, et al.
Current Protocols in Human Genetics
|
March 17, 2020
Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) Deletions
Qian Liu, Christopher M Grochowski, Weimin Bi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 14, 2017
CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region
Przemyslaw Szafranski, Justyna A Karolak, Denise Lanza, et al.
Research Square
|
March 13, 2023
SNV/indel hypermutator phenotype in biallelic RAD51C variant - Fanconi anemia
Roni Zemet, Haowei Du, Tomasz Gambin, et al.
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Search research articles
Search
Showing results (11-20 of 99) with videos related to
Sort By:
Page
of 10
BMC Genomics
|
August 25, 2022
Revised time estimation of the ancestral human chromosome 2 fusion
Barbara Poszewiecka, Krzysztof Gogolewski, Paweł Stankiewicz, et al.
Respiratory Research
|
January 22, 2021
Potential interactions between the TBX4-FGF10 and SHH-FOXF1 signaling during human lung development revealed using ChIP-seq
Justyna A Karolak, Tomasz Gambin, Przemyslaw Szafranski, et al.
Prenatal Diagnosis
|
April 8, 2022
Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges
Roni Zemet, Ignatia B Van den Veyver, Paweł Stankiewicz
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
November 21, 2013
Chromosome conformation capture-on-chip analysis of long-range cis-interactions of the SOX9 promoter
Marta Smyk, Przemyslaw Szafranski, Michał Startek, et al.
American Journal of Medical Genetics. Part A
|
June 11, 2015
A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures
Marta Smyk, Elizabeth Roeder, Sau Wai Cheung, et al.
Human Mutation
|
March 19, 2021
Lung-specific distant enhancer cis regulates expression of FOXF1 and lncRNA FENDRR
Przemyslaw Szafranski, Tomasz Gambin, Justyna A Karolak, et al.
Genome Biology
|
September 12, 2023
PhaseDancer: a novel targeted assembler of segmental duplications unravels the complexity of the human chromosome 2 fusion going from 48 to 46 chromosomes in hominin evolution
Barbara Poszewiecka, Krzysztof Gogolewski, Justyna A Karolak, et al.
Current Protocols in Human Genetics
|
March 17, 2020
Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) Deletions
Qian Liu, Christopher M Grochowski, Weimin Bi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 14, 2017
CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region
Przemyslaw Szafranski, Justyna A Karolak, Denise Lanza, et al.
Research Square
|
March 13, 2023
SNV/indel hypermutator phenotype in biallelic RAD51C variant - Fanconi anemia
Roni Zemet, Haowei Du, Tomasz Gambin, et al.
Page
of 10