Suchergebnisse - "Szafranski, Przemyslaw"

PubPharm (7)

1

Lung-specific distant enhancer cis regulates expression of FOXF1 and lncRNA FENDRR

enthalten in: Human mutation | 2021

von Szafranski, P. | Gambin, T. | Karolak, J. | +2

2

Lung‐specific distant enhancer cis regulates expression of FOXF1 and lncRNA FENDRR

enthalten in: Human mutation | 2021

von Szafranski, P. | Gambin, T. | Karolak, J. | +2

3

LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV

enthalten in: Human mutation | 2018

von Szafranski, P. | Kośmider, E. | Liu, Q. | +27

4

Novel FOXF1 deep intronic deletion causes lethal lung developmental disorder, alveolar capillary dysplasia with misalignment of pulmonary veins

enthalten in: Human mutation | 2013

von Szafranski, P. | Yang, Y. | Nelson, M. | +4

5

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain

enthalten in: Human mutation | 2013

von Sen, P. | Yang, Y. | Navarro, C. | +79

6

Novel FOXF1 Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

enthalten in: Human mutation | 2013

von Sen, P. | Yang, Y. | Navarro, C. | +79

7

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7 : benign or pathological?

enthalten in: Human mutation | 2010

von Szafranski, P. | Schaaf, C. | Person, R. | +15

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