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PubPharm (99)
1
Diminished TMEM100 Expression in a Newborn With Acinar Dysplasia and a Novel TBX4 Variant : A Case Report
enthalten in:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
| 2023
von
Szafranski, P.
|
Patrizi, S.
|
Gambin, T.
| +6
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2
Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia
enthalten in:
Clinical epigenetics
| 2023
von
Szafranski, P.
|
Garimella, R.
|
Mani, H.
| +5
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3
A Small De Novo CNV Deletion of the Paternal Copy of FOXF1, Leaving lncRNA FENDRR Intact, Provides Insight into Their Bidirectional Promoter Region
enthalten in:
Non-coding RNA
| 2023
von
Szafranski, P.
|
Stankiewicz, P.
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4
Histologic features and decreased lung FOXF1 gene expression in severe bronchopulmonary dysplasia without a genetic diagnosis of alveolar capillary dysplasia
enthalten in:
Pediatric pulmonology
| 2023
von
Galambos, C.
|
Logan, J.
|
Stankiewicz, P.
| +6
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5
KM-408, a novel phenoxyalkyl derivative as a potential anticonvulsant and analgesic compound for the treatment of neuropathic pain
enthalten in:
Pharmacological reports : PR
| 2023
von
Waszkielewicz, A.
|
Marona, H.
|
Pańczyk-Straszak, K.
| +16
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6
New Dielis species and structural dichotomy of the mitochondrial cox2 gene in Scoliidae wasps
enthalten in:
Scientific reports
| 2023
von
Szafranski, P.
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7
Ultra-conserved non-coding sequences within the FOXF1 enhancer are critical for human lung development
enthalten in:
Genes & diseases
| 2022
von
Szafranski, P.
|
Majewski, T.
|
Yıldız Bölükbaşı, E.
| +7
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8
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
Wird geladen...
9
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
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10
High-level gonosomal mosaicism for a pathogenic non-coding CNV deletion of the lung-specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPV
enthalten in:
Molecular genetics & genomic medicine
| 2022
von
Yıldız Bölükbaşı, E.
|
Karolak, J.
|
Szafranski, P.
| +6
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Medienart: E-Ressourcen
Medienart
99
Aufsätze
99
E-Artikel
E-Ressourcen
Zeitschriftentitel
8
Human genetics <Berlin>
6
Human mutation
5
American journal of medical genetics. Part A
5
Clinical epigenetics
5
European journal of human genetics : EJHG
4
American journal of human genetics
4
Human genetics
4
Respiratory research
3
BMC genomics
3
BMC medical genetics
3
Genome research
2
American journal of respiratory and critical ca...
2
Chromosome research
2
European journal of pharmaceutical sciences : o...
2
Genes
2
Mammalian genome
2
Molecular Genetics & Genomic Medicine
2
Molecular genetics & genomic medicine
2
Pediatric pulmonology
2
Pharmacological reports
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Thema
69
Journal Article
36
Research Support, N.I.H., Extramural
27
Forkhead Transcription Factors
27
Research Support, Non-U.S. Gov't
25
FOXF1 protein, human
11
Case Reports
8
ACDMPV
7
RNA, Long Noncoding
6
T-Box Domain Proteins
6
TBX4 protein, human
5
Gene regulation
4
Membrane Proteins
4
Synthesis
3
5-HT
3
Aminoalkanols
3
Analgesic
3
Anticonvulsant
3
Degradation studies
3
Deletion Allele
3
FGF10 protein, human
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Erscheinungszeitraum
98
2000-
1
1900-1999
Erscheinungsjahr(e)
Von:
Bis:
Sprache
93
Englisch
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