UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Tropomodulin Protects α-Catenin-Dependent Junctional-Actin Networks under Stress during Epithelial Morphogenesis

Current biology, 2012-08, Vol.22 (16), p.1500-1505

2012

Volltextzugriff (PDF)

Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1026-n/a

2020

Volltextzugriff (PDF)

Slice Testing-Considerations from Ordering to Reporting: A Joint Report of the Association for Molecular Pathology, College of American Pathologists, and National Society of Genetic Counselors

The Journal of molecular diagnostics : JMD, 2024-03, Vol.26 (3), p.159-167

2024

Volltextzugriff (PDF)

Detecting the “undetectable” alterations: Use of NGS to uncover high-risk alterations

Cancer genetics, 2022-06, Vol.264-265, p.5-7

2022

Volltextzugriff (PDF)

5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulation

Human genetics, 2021-04, Vol.140 (4), p.681-690

2021

Volltextzugriff (PDF)

14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patients

American journal of medical genetics. Part A, 2021-05, Vol.185 (5), p.1519-1524

2021

Volltextzugriff (PDF)

Transient myeloproliferative disorder as the presenting feature for mosaic trisomy 21

Cold Spring Harbor molecular case studies, 2021-12, Vol.7 (6), p.a006126

2021

Volltextzugriff (PDF)

Functional Manipulation of Maternal Gene Products Using In Vitro Oocyte Maturation in Zebrafish

Journal of visualized experiments, 2017-04 (122)

2017

Volltextzugriff (PDF)

Current clinical practices and challenges in molecular testing: a GOAL Consortium Hematopathology Working Group report

Blood advances, 2023-08, Vol.7 (16), p.4599-4607

2023

Volltextzugriff (PDF)

Methods for generating triploid green sea urchin embryos: An initial step in producing triploid adults for land-based and near-shore aquaculture

Aquaculture, 2011-07, Vol.318 (1), p.199-206

2011

Volltextzugriff (PDF)

Methods for karyotyping and for localization of developmentally relevant genes on the chromosomes of the purple sea urchin, Strongylocentrotus purpuratus

The Biological bulletin (Lancaster), 2009-12, Vol.217 (3), p.306-312

2009

Volltextzugriff (PDF)

Slice Testing—Considerations from Ordering to Reporting

The Journal of molecular diagnostics : JMD, 2024-03, Vol.26 (3), p.159-167

2024

Volltextzugriff (PDF)

KMT2A-CBL fusion in rapidly progressive myeloid disorder

Cancer genetics, 2022-08, Vol.266-267, p.90-92

2022

Volltextzugriff (PDF)

9. Best practices for testing and reporting of FISH studies in multiple myeloma: Recommendations from the CGC working group

Cancer genetics, 2024-08, Vol.286-287, p.S3-S4

2024

Volltextzugriff (PDF)

15. Interpreting TP53 variants identified by NGS in the setting of complex karyotypes: examples of potential cryptic copy number alterations and copy-neutral loss of heterozygosity

Cancer genetics, 2021-04, Vol.252-253, p.S5-S6

2021

Volltextzugriff (PDF)

Functional Manipulation of Maternal Gene Products Using In Vitro Oocyte Maturation in Zebrafish

Journal of visualized experiments, 2017-04 (122)

2017

Volltextzugriff (PDF)

Detecting the "undetectable" alterations: Use of NGS to uncover high-risk alterations

Cancer genetics, 2022, Vol.264-265, p.5-7

2022

Volltextzugriff (PDF)

KMT2A-CBL fusion in rapidly progressive myeloid disorder

Cancer genetics, 2022, Vol.266-267, p.90-92

2022

Volltextzugriff (PDF)

14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patients

American journal of medical genetics. Part A, 2021, Vol.185 (5), p.1519-1524

2021

Volltextzugriff (PDF)

Slow calcium waves mediate furrow microtubule reorganization and germ plasm compaction in the early zebrafish embryo

Development (Cambridge), 2018-05, Vol.145 (10), p.dev156604-dev156604

2018

Volltextzugriff (PDF)

Aggregation, segregation, and dispersal of homotypic germ plasm RNPs in the early zebrafish embryo

Developmental dynamics, 2019-04, Vol.248 (4), p.306-318

2019

Volltextzugriff (PDF)

US Severe Acute Respiratory Syndrome Coronavirus 2 Epsilon Variant: Highly Transmissible but With an Adjusted Muted Host T-Cell Response

Clinical infectious diseases, 2022-11, Vol.75 (11), p.1940-1949

2022

Volltextzugriff (PDF)

Expert Curation of Somatic FLT3 Variants By the Clingen Somatic Hematologic Cancer Taskforce (ClinGen HCT)

Blood, 2021-11, Vol.138 (Supplement 1), p.4387-4387

2021

Volltextzugriff (PDF)

Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization

Genetics in medicine, 2019-04, Vol.21 (4), p.861-866

2019

Volltextzugriff (PDF)

1 – 25 von 25

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(22)
Mit Volltextzugriff
(24)

Publikationsform

Artikel
(22)
Berichte
(3)

Sprache

Englisch
(25)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Tropomodulin Protects α-Catenin-Dependent Junctional-Actin Networks under Stress during Epithelial Morphogenesis

Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers

Slice Testing-Considerations from Ordering to Reporting: A Joint Report of the Association for Molecular Pathology, College of American Pathologists, and National Society of Genetic Counselors

Detecting the “undetectable” alterations: Use of NGS to uncover high-risk alterations

5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulation

14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patients

Transient myeloproliferative disorder as the presenting feature for mosaic trisomy 21

Functional Manipulation of Maternal Gene Products Using In Vitro Oocyte Maturation in Zebrafish

Current clinical practices and challenges in molecular testing: a GOAL Consortium Hematopathology Working Group report

Methods for generating triploid green sea urchin embryos: An initial step in producing triploid adults for land-based and near-shore aquaculture

Methods for karyotyping and for localization of developmentally relevant genes on the chromosomes of the purple sea urchin, Strongylocentrotus purpuratus

Slice Testing—Considerations from Ordering to Reporting

KMT2A-CBL fusion in rapidly progressive myeloid disorder

9. Best practices for testing and reporting of FISH studies in multiple myeloma: Recommendations from the CGC working group

15. Interpreting TP53 variants identified by NGS in the setting of complex karyotypes: examples of potential cryptic copy number alterations and copy-neutral loss of heterozygosity

Functional Manipulation of Maternal Gene Products Using In Vitro Oocyte Maturation in Zebrafish

Detecting the "undetectable" alterations: Use of NGS to uncover high-risk alterations

KMT2A-CBL fusion in rapidly progressive myeloid disorder

14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patients

Slow calcium waves mediate furrow microtubule reorganization and germ plasm compaction in the early zebrafish embryo

Aggregation, segregation, and dispersal of homotypic germ plasm RNPs in the early zebrafish embryo

US Severe Acute Respiratory Syndrome Coronavirus 2 Epsilon Variant: Highly Transmissible but With an Adjusted Muted Host T-Cell Response

Expert Curation of Somatic FLT3 Variants By the Clingen Somatic Hematologic Cancer Taskforce (ClinGen HCT)

Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization

48. Crowdsourcing expert curation of somatic variants by the ClinGen Somatic Hematologic Cancer Taskforce

Suchergebnisse filtern