Recursos de colección
PubMed Central (PMC3 - NLM DTD)
(2,081,148 recursos)
Archive of life sciences journal literature at the U.S. National Institutes of Health (NIH), developed and managed by NIH's National Center for Biotechnology Information (NCBI) in the National Library of Medicine (NLM).
Mostrando recursos 121 - 140 de 900
121.
Isozyme and allozyme markers distinguishing two morphologically similar, medically important Mastomys species (Rodentia: Muridae)
- Smit, Andre A; Van der Bank, Herman FH
122.
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing
- Bennett, Richard R; den Dunnen, Johan; O'Brien, Kristine F; Darras, Basil T; Kunkel, Louis M
123.
Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure
- Chang, Bo; Smith, Richard S; Peters, Maureen; Savinova, Olga V; Hawes, Norman L; Zabaleta, Adriana; Nusinowitz, Steven; Martin, Janice E; Davisson, Muriel L; Cepko, Constance L; Hogan, Brigid LM; John, Simon WM
124.
Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography
- Le Maréchal, Cedric; Chen, Jian-Min; Quéré, Isabelle; Raguénès, Odile; Férec, Claude; Auroux, Jean
125.
Fusion of the NUP98 gene with the LEDGF/p52 gene defines a recurrent acute myeloid leukemia translocation
- Hussey, Damian J; Moore, Sarah; Nicola, Mario; Dobrovic, Alexander
126.
A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues
- Chibuk, Thea K; Bischof, Jocelyn M; Wevrick, Rachel
127.
A sensitive and rapid assay for homologous recombination in mosquito cells: impact of vector topology and implications for gene targeting
- Eggleston, Paul; Zhao, Yuguang
128.
Analysis of genetic heterogeneity in the HCAR adenovirus-binding Ig1 domain in a Caucasian Flemish population
- Thoelen, Inge; Duson, Griet; Wollants, Elke; Van Ranst, Marc
129.
Identification and preliminary characterization of mouse Adam33
- Gunn, Teresa M; Azarani, Arezou; Kim, Philip H; Hyman, Richard W; Davis, Ronald W; Barsh, Gregory S
130.
ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase
- Hosseini-Maaf, Bahram; Hellberg, Ã?sa; Rodrigues, Maria J; Chester, M Alan; Olsson, Martin L
131.
Parasexual genetics of Dictyostelium gene disruptions: identification of a ras pathway using diploids
- King, Jason; Insall, Robert H
132.
Study of human SP-A, SP-B and SP-D loci: allele frequencies, linkage disequilibrium and heterozygosity in different races and ethnic groups
- Liu, Wenlei; Bentley, Christy M; Floros, Joanna
133.
Mitochondrial DNA transit between West Asia and North Africa inferred from U6 phylogeography
- Maca-Meyer, Nicole; González, Ana M; Pestano, José; Flores, Carlos; Larruga, José M; Cabrera, Vicente M
134.
Genetic diversity and relationships in mulberry (genus Morus) as revealed by RAPD and ISSR marker assays
- Awasthi, Arvind K; Nagaraja, GM; Naik, GV; Kanginakudru, Sriramana; Thangavelu, K; Nagaraju, Javaregowda
135.
Quantitative trait loci in Anopheles gambiae controlling the encapsulation response against Plasmodium cynomolgi Ceylon
- Zheng, Liangbiao; Wang, Shuang; Romans, Patricia; Zhao, Hongyu; Luna, Coralia; Benedict, Mark Q
136.
RHD allele distribution in Africans of Mali
- Wagner, Franz F; Moulds, Joann M; Tounkara, Anatole; Kouriba, Bourema; Flegel, Willy A
137.
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX
- Engle, Elizabeth C; McIntosh, Nathalie; Yamada, Koki; Lee, Bjorn A; Johnson, Roger; O'Keefe, Michael; Letson, Robert; London, Arnold; Ballard, Evan; Ruttum, Mark; Matsumoto, Naomichi; Saito, Nakamichi; Collins, Mary Louise Z; Morris, Lisa; Monte, Monte Del; Magli, Adriano; de Berardinis, Teresa
138.
Multiple telophase arrest bypassed (tab) mutants alleviate the essential requirement for Cdc15 in exit from mitosis in S. cerevisiae
- Shou, Wenying; Deshaies, Raymond J
139.
Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS)
- Silahtaroglu, Asli N; Brondum-Nielsen, Karen; Gredal, Ole; Werdelin, Lene; Panas, Marios; Petersen, Michael B; Tommerup, Niels; Tümer, Zeynep
140.
Occurrence of leu+ revertants under starvation cultures in Escherichia coli is growth-dependent
- Jin, Jianling; Gao, Peiji; Mao, Yumin