Suchergebnisse - "Humans"

PubPharm (6.298)

1

An unusual case of primary splenic soft part alveolar sarcoma : case report and review of the literature with emphasis on the spectrum of TFE3-associated neoplasms

enthalten in: Diagnostic pathology | 2024

von Guérin, R. | Menard, A. | Angot, E. | +6

2

Minor introns impact on hematopoietic malignancies

enthalten in: Experimental hematology | 2024

von Nishimura, K. | Saika, W. | Inoue, D.

3

Clinical characteristics and prognosis analysis of 17 cases of SMARCA4-deficient chest tumors

enthalten in: Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases | 2024

von Cao, X. | Li, Z. | Wang, Q.

4

Evidence for common mechanisms of pathology between SHANK3 and other genes of Phelan-McDermid syndrome

enthalten in: Clinical genetics | 2024

von Mitz, A. | Boccuto, L. | Thurm, A.

5

SALL4 in gastrointestinal tract cancers : upstream and downstream regulatory mechanisms

enthalten in: Molecular medicine (Cambridge, Mass.) | 2024

von Wang, T. | Jin, Y. | Wang, M. | +8

6

Advance in molecular genetics of mesothelioma

enthalten in: Zhonghua bing li xue za zhi = Chinese journal of pathology | 2024

von Zhang, J. | Gong, Q.

7

JAK2/STAT3 as a new potential target to manage neurodegenerative diseases : An interactive review

enthalten in: European journal of pharmacology | 2024

von Panda, S. | Kesharwani, A. | Datta, S. | +3

8

A case of polyglucosan body myopathy caused by an RBCK1 gene variant and literature review

enthalten in: Molecular genetics & genomic medicine | 2024

von Sun, Q. | Xie, Z. | Song, L. | +1

9

Clinical report and genetic analysis of a novel variant in ZMIZ1 causing neurodevelopmental disorder with dysmorphic factors and distal skeletal anomalies in a Chinese family

enthalten in: Genes & genomics | 2024

von He, L. | Wang, Y. | Pan, J. | +3

10

ASXL3-related disorder : Molecular phenotyping and comprehensive review providing insights into disease mechanism

enthalten in: Clinical genetics | 2024

von Woods, E. | Holmes, N. | Albaba, S. | +2

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