(1) Elucidation of the genomic organization of the Oct-11a POU domain revealed a striking concordance of intron/exon junctions with Oct-2.

(2) The isolation of one exon is theoretically sufficient to screen cosmid and cDNA libraries for further analysis of the corresponding gene.

(3) Here we show that the P3A exon is present only in primates and man and it is conserved through primate evolution.

(4) Phenomena such as exon shuffling imply that genomes are constantly being rearranged, and are not mere static repositories of information.

(5) Either exon 1 or coding segment 2 can splice with exon 3 to encode an alanine across the splice junction.

(6) It is a missense mutation in exon III.

(7) Conclusion Mutation of Exon A in AR gene plays an important part in infertile men with oligospermia.

(8) A missense mutation(G1010A) in exon 3 of HR was identified in the patient's father.

(9) No pathogenic mutation was detected in the exon and franking regions of MYH9 gene except a synonymous mutation(A1143A) in the exon 25.

(10) Objective: To exclude known gene mutation, 21 exon of SOS1 which had been certified by foreign country form 2 families with hereditary gingival fibromatosis .

(11) Conclusion:Mutation of Exon A in AR gene plays a very important part in development of infertile men with oligospermia .

(12) How to use high throughput exon array to analysis different mRNA isoforms expression is very important.

(13) Method Exon 17 of RET proto - oncogene from 30 Hirschsprung disease was detected by PCR - SSCP method.

(14) Conclusion Exon rearrangement of parkin gene exists in Chinese patients with isolated EOP.

(15) Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

(16) Objective To explore the mutation of RET exon 13 in sporadic medullary thyroid carcinoma.

(17) Polymorphism in Exon 6 of MAOA gene of Turpan cockfighting and Xinluoman was analyzed by PCR-SSCP.

(18) Objective To investigate the point mutation features of exon 11 and 12 in phenylalanine hydroxylase( PAH )gene of the patients with phenylketonuria(PKU)in Xinjiang.

(19) Objective: To detect the mutation in exon 15 of cholesteryl ester transfer protein gene and its properties.

(20) Comclusion SNP site on vitamine D receptor gene exon 2 is one with high polymorphism and certain popu-lational diversity.

(21) Corresponding amino acid sequence of AChRa are noted below exon sequences.

(22) Two alleles of the COMT gene as a result of a G/A transition in the exon 4 can lead to different COMT enzymatic activities.

(23) To understand intron 15 of human LDL receptor gene(/exon.html), the DNA fragments from exon 15 to exon 16 and the 3' end of intron 15 were amplified with long chain PCR and anchored PCR.

(24) Methods:1PCR-restriction enzyme digestion and denaturing high-performance liquid chromatography(DHPLC) methods were applied to detect the deletion of the exon 7 and 8 of SMN1 gene.

(25) Therefore the other aim of our study is to discover SNPs of HCN4 exon 1, including the regulatory sequence and exon-intron boundary of it, which plays an importable role of channel function.

(26) These gene mutation distributing in all over the whole coding section of ATM gene. Every Exon exist the gene mutated site and no obvious hot mutated site be discovered.

(27) Results Among the 130 cases of primary amenorrhea, 33 had abnormal karyotypes. A point mutation at exon 7 of GHRHR gene was found in one patient.

(28) Objective To investigate the frequencies of three point mutations, CGT52TGT, GGC54GAC and GGA57GAA, in exon 1 of mannan-binding lectin structural gene in Chinese Uyghur population.

(29) Objectives: To study the association between M235T allele polymorphism in exon 2 of angiotensinogen(AGT) gene and essential hypertension(EH).

(30) The polyadenylation signal ( pA ) within the vector defines the final exon of the endogenous transcription unit.

(31) Allele A5 and A5.1 of exon 5 in MICA gene were associated with psychotropics-induced leucopenia.

(32) Results A homozygous mutation at exon 13 of the proband was found by parallel TGGE. Homozygous and heterozygous mutations were also found in the family by parallel TGGE.

(33) Objective To investigate the genetic polymorphism of microsatellite in the exon 5 of MICA gene and the intron 1 of MICB gene in Guangdong Han population.

(34) Objective To evaluate the relationship between T174M and M235T polymorphisms of angiotensinogen (AGT) gene in exon 2 and brain infarction (BI) in Chinese Han population.

(35) That exon could not FORM chemical compounds was once believed by scientists.