Suchergebnisse - "Szafranski, Przemyslaw"

PubPharm (33)

1

KM-408, a novel phenoxyalkyl derivative as a potential anticonvulsant and analgesic compound for the treatment of neuropathic pain

enthalten in: Pharmacological reports | 2022

von Waszkielewicz, A. | Marona, H. | Pańczyk-Straszak, K. | +16

2

Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype

enthalten in: Human genetics | 2019

von Szafranski, P. | Liu, Q. | Karolak, J. | +15

3

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

enthalten in: Human genetics | 2017

von Zhang, J. | Gambin, T. | Yuan, B. | +35

4

CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region

enthalten in: Mammalian genome | 2017

von Szafranski, P. | Karolak, J. | Lanza, D. | +3

5

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

enthalten in: Human genetics | 2017

von Zhang, J. | Gambin, T. | Yuan, B. | +35

6

Assessment of the chromatographic lipophilicity of eight cephalosporins on different stationary phases

enthalten in: European journal of pharmaceutical sciences | 2017

von Dąbrowska, M. | Starek, M. | Komsta, �. | +3

7

Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features

enthalten in: American journal of human genetics | 2017

von Stankiewicz, P. | Khan, T. | Szafranski, P. | +35

8

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

enthalten in: Human genetics | 2016

von Szafranski, P. | Gambin, T. | Dharmadhikari, A. | +90

9

Prenatal Diagnosis of Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins

enthalten in: The journal of pediatrics | 2016

von Prothro, S. | Plosa, E. | Markham, M. | +3

10

Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family

enthalten in: Pediatric pulmonology | 2016

von Reiter, J. | Szafranski, P. | Breuer, O. | +4