短臂

结果证实该额外小染色体是D组或G组染色体的短臂。

The results showed that this chromosome was from the short arm of chromosome of D / G group .

目的研究伴9号染色体短臂（p）异常的急性淋巴细胞白血病（急淋）的临床及分子细胞遗传学特征。

Objective To investigate clinical and molecular cytogenetics characteristics of patients with abnormalities of the short arm of chromosome 9 in acute lymphoblastic leukemia ( ALL ) .

3号染色体短臂末端两个大片段基因组区域的基因分布与GC含量分析

Comparing Gene Density and GC Content Between Two Large Genomic Blocks at Short Arm of Chromosome 3

所有染色体着丝粒为阳性C带，而且第1对染色体短臂也呈C带阳性，其着色强度与该对染色体上的着丝粒C带相同；

All the centromeres of chromosomes were C-bands positive and so was the short arm of the 1st chromosome with tinctorial strength same as its centromeric C-bands ;

PCR－LOH检测神经母细胞瘤1号染色体短臂缺失

PCR-LOH of Chromosome 1p Deletion in Neuroblastoma

9号染色体短臂上7个STR基因座在基因扫描中的信息表现

Information Behavior of 7 STR Loci on Chromosome 9p in Gene Scanning

在人类肿瘤中，抑癌基因p53是突变最频发的基因，它位于17号染色体短臂上。

It is known that the tumor suppressor gene P53 is the most active and frequent mutation gene in human cancer .

P53基因定位于人类第17号染色体的短臂，野生型P53基因是肿瘤抑制基因。

P53 gene is localized in the short arm of human chromosome 17 . The wild type P53 gene is tumour suppressor gene .

用G带和C带技术鉴定为第9号染色体短臂三体（9p+）和一条X染色体长臂远端部分缺失（xq&）。

Trisomy of the short arm of chromosome 9 ( 9p + ) and distal deletion of the long arm of X-chromosome were found with G banding and C-banding techniques .

17号染色体短臂LOH是晚期大肠癌的基因标记

17p LOH is the gene marker of late stage colorectal adenocarcinoma

6号染色体短臂MHCⅡ类抗原区基因多态性与精神分裂症的关系

Relationship between gene polymorphism on MHC ⅱ region on the short arm of chromosome 6 and schizophrenia

3B染色体短臂小麦赤霉病抗性主效QTL的分析

Analysis of Major QTL for Fusarium Head Blight Resistance on the Short Arm of Chromosome 3B in Wheat

织物从箱的顶部喂入，在折叠状态下进入J形的长臂，然后从J形的短臂处引出。

The cloth is fed into the box at the top , folded to fill the longer arm , and removed through the shorter arm .

染色质的一小部分，含有核糖体RNA基因，位于近端着丝粒染色体的短臂染色质末端；

Chromosomal satellite & A small mass of chromatin containing genes for ribosomal RNA , at the end of the short arm of each chromatid of an acrocentric chromosome ;

其中常染色体平衡易位2例，臂间倒位2例，染色体次缢痕增大和G组短臂增加各1例。

Two cases were autosomal balanced translocation and two cases were pericentric inversion . The chromosome secondary constriction in one case became wider and the short arms of G team chromosomes in one case became longer .

目的：观察经人力短臂离心机锻炼后心率变异性（HRV）参数的变化。

AIM : To investigate the changes of parameters of heart rate variability ( HRV ) after self powered short arm human centrifuge training .

睾丸决定因子基因（Testis-determiningfactor，TDF）位于Y染色体短臂上，它的表达产物诱导睾丸组织的发生。

The testis-determining factor gene ( TDF ) lies on the Y chromosome and is responsible for initiating male sex detemination .

哺乳动物中位于Y染色体短臂临界区域的SRY基因启动雄性性状的发育。

The pathway of male sexual development in mammals is initiated by SRY , agene on the short arm boundary of Y chromosome .

哺乳动物Y染色体短臂上的Sry基因决定雄性发育方向。

Sex-determining region Y ( Sry ) gene located in the short arm of the mammalian Y chromosome directs the sexual development of male .

因此，可以推测这个分子标记（OPW03-570）是位于簇毛麦V染色体短臂上的。

Therefore , this molecular marker ( OPW03-570 ) may locate in the short arm of Haynaldia villosa 's V chromosome .

人类MHC，又称人类白细胞抗原（HLA），位于第六号染色体短臂，是一群高度多态性的紧密连锁基因群。

Human MHC , also named human leukocyte antigen ( HLA ), which locates in the short arm of chromosome VI , which is a tightly linked group of highly polymorphic gene cluster .

丹麦长白猪Ag-NOR仅定位于第10号染色体短臂次缢痕区。枫泾猪、丹麦长白猪Ag-NOR颗粒数是有差别的。

Danish Landrace NORs were located on chromosome 10 . The number of Ag-NORs were difference between two breeds .

带有银染核仁组织者（Ag-NORs）染色体的数目为2&6条，NORs均位于6、8、15亚中着丝粒染色体短臂。

Two to six NORs are distributed on the short arm of submetacentric ( Nos. 6 , 8 , 15 ) .

人类白细胞抗原（humanleukocyteantigen，HLA）复合体是位于人类第6号染色体短臂6p21.31的一组紧密连锁的基因群，HLA分子具有高度的多态性，迄今已知近千种HLA等位基因。

HLA comprises a family of genes within the human leukocyte antigen complex located on the short arm of chromosome ( 6p21.31 ) in humans . HLA molecules are highly polymorphic with nearly 1000 alleles .

目的：研究肺癌组织中第3号染色体短臂（3P）和第9号染色体短臂（9P）上微卫星标志物的改变与肺癌发生发展的关系。

Objective : To investigate the relationship among microsatellite marker alterations on chromosome 3P and 9P and oncogenesis , development in lung cancer .

结果人力短臂离心机训练3d后，心率显著降低（P<0.05），左室射血时间（LVET）显著延长（P<0.01）；

Results Heart rate ( HR ) decreased significantly while left ventricular ejection time ( LVET ) increased significantly after 3 d training , and the changes of HR and LVET were more obvious after 7 d training .

结果5号染色体短臂17个微卫星标记的平均信息性病例比例为60.0%（48/80），35.0%（28/80）的病例至少一个位点检测到LOH。

Results The average informative rate of all seventeen markers was 60.0 % . The LOH at least in one locus was detected in 28 of the 80 ( 35.0 % ) cases .

人类原始未分化性腺是具有双潜能的性腺，SRY基因是男性Y染色体短臂上的性别决定基因，其表达诱导原始未分化性腺向睾丸发育，是男性性别发育的始动因素。

Undifferentiated gonad in human is bipotential . SRY is a sex-determining gene in short arm of Y chromosome which induces bipotential gonads to testis . It is also the initiating factor in male development .

猫叫综合征（cri-du-chat，CDC，MIM123450）由Lejeune等最早报道，由一条5号染色体短臂发生缺失引起。

The cri-du - chat syndrome ( CDC , MIM123450 ), first described by Lejeune , is caused by deletions in 5p .

9名健康男性青年利用人力短臂离心机进行训练，转速为30～34r·min-1，持续时间为5min，1次/d，连续训练7d。

Nine healthy male volunteers received self powered short arm human centrifuge training for 5 min per day with rotative velocity of 30 ~ 34 r · min - 1 for 7 d.