نتائج البحث

Transcriptomics-based exploration of ubiquitination-related biomarkers and potential molecular mechanisms in laryngeal squamous cell carcinoma.

• Authors : Chen, Qiu^1,2 (AUTHOR); Wu, Zhimin¹ (AUTHOR); Ma, Yifei² (AUTHOR)

• Source: BMC Medical Genomics. 5/12/2025, Vol. 18 Issue 1, p1-19. 19p.

تفاصيل العنوان

Development and validation of cuproptosis-related lncRNA signatures for prognosis prediction in colorectal cancer.

• Authors : Pang, Lin^1,2 (AUTHOR); Wang, Qingqing² (AUTHOR); Wang, Lingxiao¹ (AUTHOR)

• Source: BMC Medical Genomics. 3/22/2023, Vol. 16 Issue 1, p1-19. 19p.

تفاصيل العنوان

Impact of the interaction between the polymorphisms and hypermethylation of the CD36 gene on a new biomarker of type 2 diabetes mellitus: circulating soluble CD36 (sCD36) in Senegalese females.

• Authors : Touré, Maïmouna^1,2 (AUTHOR) ; Samb, Abdoulaye^1,2 (AUTHOR); Sène, Mbaye³ (AUTHOR)

• Source: BMC Medical Genomics. 8/29/2022, Vol. 15 Issue 1, p1-13. 13p.

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Identification of two novel large deletions in FBN1 gene by next-generation sequencing and multiplex ligation-dependent probe amplification.

• Authors : Lu X; Center of Clinical Laboratory, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, 361004, China.; Wang R

Subjects: Multiplex Polymerase Chain Reaction* ; Marfan Syndrome*/Marfan Syndrome*/Marfan Syndrome*/genetics ; Marfan Syndrome*/Marfan Syndrome*/Marfan Syndrome*/diagnosis

• Source: BMC medical genomics [BMC Med Genomics] 2024 Feb 05; Vol. 17 (1), pp. 47. Date of Electronic Publication: 2024 Feb 05.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Prenatal diagnosis of 1408 foetuses at risk of DMD/BMD by MLPA and Sanger sequencing combined with STR linkage analysis.

• Authors : Hua C; Genetics and Prenatal Diagnosis Center, Department of Obstetrics and Gynaecology, The First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.; Liu L

Subjects: Multiplex Polymerase Chain Reaction* ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/diagnosis ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics

• Source: BMC medical genomics [BMC Med Genomics] 2023 Dec 01; Vol. 16 (1), pp. 310. Date of Electronic Publication: 2023 Dec 01.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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A splice-site variant (c.3289-1G>T) in OTOF underlies profound hearing loss in a Pakistani kindred.

• Authors : Ahmed, Ashfaque¹ (AUTHOR); Wang, Meng¹ (AUTHOR); Khan, Rizwan¹ (AUTHOR)

• Source: BMC Medical Genomics. 1/4/2021, Vol. 14 Issue 1, p1-8. 8p.

تفاصيل العنوان

Effective detection of 148 cases chromosomal mosaicism by karyotyping, chromosomal microarray analysis and QF-PCR in 32,967 prenatal diagnoses.

• Authors : Deng, Yi; Zeng, Lan; Wu, Zhiling

Subjects: MOSAICISM; DNA copy number variations; PRENATAL genetic testing

• Source: BMC Medical Genomics; 4/10/2025, Vol. 18 Issue 1, p1-13, 13p

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Study on the mechanism of BGN in progression and metastasis of ccRCC.

• Authors : Xia, Hanqing; He, Tianzhen; Li, Xueyu

Subjects: MEDICAL sciences; RENAL cell carcinoma; CELL migration

• Source: BMC Medical Genomics; 3/19/2025, Vol. 18 Issue 1, p1-12, 12p

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LRIG1 expression and colorectal cancer prognosis.

• Authors : Bakherad, Maryam¹ (AUTHOR); Salimi, Mahdieh² (AUTHOR) ; Angaji, Seyed Abdolhamid¹ (AUTHOR)

• Source: BMC Medical Genomics. 1/18/2021, Vol. 14 Issue 1, p1-6. 6p.

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First report of Leishmania RNA virus 2 and its high genetic diversity in cutaneous leishmaniasis cases from Ilam Province, Iran.

• Authors : Saberi, Reza; Fallahi Lima, Amirmohammad; Hajjaran, Homa

Subjects: CUTANEOUS leishmaniasis; LEISHMANIA major; PHYLOGENYIRAN; ILAM (Iran)

• Source: BMC Medical Genomics; 8/21/2025, Vol. 18 Issue 1, p1-7, 7p

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