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Smarcc2基因

Websmarcc2 作用功能 編輯 該基因編碼的蛋白是SWI/SNF蛋白家族的成員，其成員顯示螺旋酶和ATP酶的活性，並被認為通過改變這些基因周圍的染色質結構來調節某些基因的轉錄。 WebJan 15, 2024 · Human SMARCC2 full-length ORF ( AAH13045, 1 a.a. - 1130 a.a.) recombinant protein with GST-tag at N-terminal. 基因名称 : SMARCC2. 基因别名 : BAF170 CRACC2 Rsc8. 基因描述 : SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2.

SMARCC2_百度百科

Web基因/基因ID: ARID1A(8289) 表达特异性: ... ACTL6A/BAF53, SMARCC1/BAF155, SMARCC2/BAF170, and SMARCB1/SNF5/BAF47. Other subunits specific to each of the complexes may also be present permitting several possible combinations developmentally and tissue specific. Component of the BAF (SWI/SNF-A) complex, which includes at least … Web该图显示了 smarcc2/baf170 的已知靶标基因 tmem53 的结合（参见包含 cut&run-qpcr 数据的其他结果图）。 对在无酚红培养基和 5% 活性炭剥离 FBS 中生长 4 天后接着使用 β 雌 … fmf icd-10 https://texaseconomist.net

SMARCC2 mediates the regulation of DKK1 by the transcription

WebMar 3, 2024 · Background Coffin-Siris syndrome-8 (CSS8) is a rare autosomal dominant disorder caused by variants in SMARCC2, a core subunit of the chromatin-remodeling complex BRG1-associated factor (BAF). The clinical characteristics of this disorder have not been entirely determined because of the rarity of clinical reports. The BAF complex plays … Websmarcc2 作用功能 编辑 播报 该基因编码的蛋白是SWI/SNF蛋白家族的成员，其成员显示螺旋酶和ATP酶的活性，并被认为通过改变这些基因周围的染色质结构来调节某些基因的转录。 http://www.jinpanmed.cn/archives/date/2024/03/28/page/8 fmf in pregnancy

SMARCC2 Gene - GeneCards SMRC2 Protein SMRC2 …

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Smarcc2基因

Expanding the Spectrum of BAF-Related Disorders: De

WebDec 8, 2024 · SMARCC2. -related neurodevelopmental disorder through exome analysis and reanalysis in two patients. Dong Li, Helen Downes, Cuiping Hou, Hakon Hakonarson, … Web68094 Ensembl ENSG00000139613 ENSMUSG00000025369 UniProt Q8TAQ2 Q6PDG5 RefSeq (mRNA) NM_001130420 NM_003075 NM_139067 NM_001330288 NM_001114096 NM_001114097 NM_198160 NM_001372395 RefSeq (protein) NP_001123892 NP_001317217 NP_003066 NP_620706 NP_001107568 NP_001107569 NP_937803 …

Smarcc2基因

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Web在primed hPSC中， ZIC2、ZIC5、LIN28A和L1TD1等转录因子更多。核心多能性因子（POU5F1、SALL4和SOX2）和染色质重塑因子（BRD3、BRD4和SMARCC2）在两个细胞系中结合水平相当。 与先前的发现一致，与primed hPSC相比，naive hPSC总体上DNA甲基化程 … WebJan 3, 2024 · SMARCC2 (MIM: 601734) encodes BAF170, a common core subunit of the BAF complexes with high homology to SMARCC1 (BAF155). 26 It is an intrinsic factor of glial radial cells and plays a crucial role in embryogenesis and corticogenesis, determining the mammalian body and cortical size. 27 Smarcc2;Smarcc1 double knockout mice …

Web用于研究领域中研究 smarcc2 的 sirna。 Web卵巢高钙血症型小细胞癌（Small cell carcinoma of the ovary of hypercalcemic type, SCCOHT）属于一种侵袭性非常强的恶性肿瘤，通常发生于年轻的女性，其特征是具 …

WebNov 23, 2024 · SMARCC2 can maintain the integrity of the SWI/SNF complex. SMARCC2, as the basic module of the SWI/SNF chromatin remodeling complex, stabilizes the whole … http://html.rhhz.net/ZLFZYJ/html/8578.2024.18.1871.htm

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WebApr 4, 2024 · SMARCC2 mediates the regulation of DKK1 by the transcription factor EGR1 through chromatin remodeling to reduce the proliferative capacity of glioblastoma. … greensburg courthouse kyWebMay 15, 2024 · The SMARCC2 gene encodes BAF170, the 170-kD subunit of the SWI/SNF chromatin remodeling complex ( Wang et al., 1996 ). See also BAF60a ( 601735 ), -b ( … fmf intranetWebsmarcc2是位於12號染色體的基因。 該基因編碼的蛋白是swi/snf蛋白家族的成員，其成員顯示螺旋酶和atp酶的活性，並被認為通過 ... fmf infant clothingWebCoffin-Siris syndrome-8 (CSS8) is characterized by variable degrees of impaired intellectual development including speech impairment, hypotonia, feeding difficulties, and behavioral abnormalities. Dysmorphic features may or may not be present and include hypertrichosis or thin scalp hair, thick eyebrows, thin upper vermilion, and upturned nose ... greensburg county kyWeb作用功能. 该基因编码的蛋白是SWI/SNF家族的成员，与果蝇的Brahma蛋白非常相似。. 这个家族的成员具有解旋酶和ATP酶的活性，并被认为通过改变这些基因周围的染色质结构来 … fm / firstmark servicedWeb概述：. SMARCB1是由位于染色体22q11.2上的基因SMARCB1的蛋白产物。. 广泛表达于正常细胞的细胞核，一些肿瘤可表达缺失。. 血管内皮和淋巴细胞核着色可作为内对照。. INII是SWI/SNFATP依赖性染色质重构复合物的核心亚单位，在正常细胞的细胞核中广泛表达（它被 … fmf indie crosshttp://www.biofeng.com/gene/renyuan/SMARCC2.html fmf in medical term