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Coinfection With Human Herpesvirus (HHV)-6B in Immunocompetent, Healthy Individuals With Chromosomally Integrated HHV-6A.
- Published in:
- Journal of the Pediatric Infectious Diseases Society, 2021, v. 10, n. 2, p. 175, doi. 10.1093/jpids/piaa009
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- Publication type:
- Article
Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients.
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- Molecular Human Reproduction, 2008, v. 14, n. 10, p. 595, doi. 10.1093/molehr/gan054
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- Publication type:
- Article
Placental Genetic Variants in the Upstream Region of the FLT1 Gene in Preeclampsia.
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- Journal of Reproduction & Infertility, 2020, v. 21, n. 4, p. 240, doi. 10.18502/jri.v21i4.4328
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- Publication type:
- Article
Low grade amplification of MDM2 gene in a subset of human breast cancers without p53 alterations.
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- Breast Cancer (13406868), 1994, v. 1, n. 2, p. 95, doi. 10.1007/BF02967038
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- Publication type:
- Article
An Analysis of Differentially Expressed Coding and Long Non-Coding RNAs in Multiple Models of Skeletal Muscle Atrophy.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2558, doi. 10.3390/ijms22052558
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- Publication type:
- Article
Prenatal diagnosis of premature chromatid separation/mosaic variegated aneuploidy (PCS/MVA) syndrome.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2018, v. 44, n. 7, p. 1313, doi. 10.1111/jog.13647
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- Publication type:
- Article
Cover Image, Volume 90, Number 10, October 2018.
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- Journal of Medical Virology, 2018, v. 90, n. 10, p. i, doi. 10.1002/jmv.25281
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- Publication type:
- Article
Chromosomally integrated human herpesvirus 6 in the Japanese population.
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- Journal of Medical Virology, 2018, v. 90, n. 10, p. 1636, doi. 10.1002/jmv.25244
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- Publication type:
- Article
Human herpesvirus 6 (HHV-6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV-6 DNA.
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- Journal of Medical Virology, 2004, v. 73, n. 3, p. 465
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- Publication type:
- Article
CD9 Gene Variations Are Not Associated with Female Infertility in Humans.
- Published in:
- Gynecologic & Obstetric Investigation, 2010, v. 69, n. 2, p. 116, doi. 10.1159/000262451
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- Publication type:
- Article
Analysis of Nitric Oxide Metabolism as a Placental or Maternal Factor Underlying the Etiology of Pre-Eclampsia.
- Published in:
- Gynecologic & Obstetric Investigation, 2009, v. 68, n. 4, p. 239, doi. 10.1159/000238381
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- Publication type:
- Article
Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature sperm.
- Published in:
- Human Genetics, 2023, v. 142, n. 10, p. 1451, doi. 10.1007/s00439-023-02591-9
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- Publication type:
- Article
The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.
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- Human Genetics, 2020, v. 139, n. 11, p. 1417, doi. 10.1007/s00439-020-02186-8
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- Publication type:
- Article
Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 12, p. 1, doi. 10.1002/mgg3.1531
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- Publication type:
- Article
Familial cardiac septal defect due to a novel nine-base deletion in TBX20.
- Published in:
- Pediatrics International, 2022, v. 64, n. 1, p. 1, doi. 10.1111/ped.14995
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- Publication type:
- Article
Prevalence of Emanuel syndrome: Theoretical frequency and surveillance result.
- Published in:
- Pediatrics International, 2014, v. 56, n. 4, p. 462, doi. 10.1111/ped.12437
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- Publication type:
- Article
Decreased frequency of seizures in infantile spasms associated with lissencephaly by human herpes virus 7 infection.
- Published in:
- Pediatrics International, 2002, v. 44, n. 2, p. 168, doi. 10.1046/j.1328-8067.2001.01511.x
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- Publication type:
- Article
HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity.
- Published in:
- Genes to Cells, 2012, v. 17, n. 11, p. 897, doi. 10.1111/gtc.12005
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- Publication type:
- Article
HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes.
- Published in:
- Genes to Cells, 2012, v. 17, n. 6, p. 439, doi. 10.1111/j.1365-2443.2012.01600.x
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- Publication type:
- Article
Signature of backward replication slippage at the copy number variation junction.
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- Journal of Human Genetics, 2014, v. 59, n. 5, p. 247, doi. 10.1038/jhg.2014.20
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- Publication type:
- Article
Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.
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- Journal of Human Genetics, 2012, v. 57, n. 8, p. 515, doi. 10.1038/jhg.2012.61
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- Publication type:
- Article
Mechanism of complex gross chromosomal rearrangements: A commentary on Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 2, p. 81, doi. 10.1038/jhg.2011.143
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- Publication type:
- Article
Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans.
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- Journal of Human Genetics, 2010, v. 55, n. 5, p. 293, doi. 10.1038/jhg.2010.26
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- Publication type:
- Article
Recent advance in our understanding of the molecular nature of chromosomal abnormalities.
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- Journal of Human Genetics, 2009, v. 54, n. 5, p. 253, doi. 10.1038/jhg.2009.35
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- Publication type:
- Article
Mutation analysis of a Japanese patient with fucosidosis.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 323, doi. 10.1007/s100380050169
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- Publication type:
- Article
Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome.
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- Journal of Human Genetics, 1999, v. 44, n. 4, p. 235, doi. 10.1007/s100380050150
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- Publication type:
- Article
Novel polymorphisms in the βig-h3 gene.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 3, p. 214, doi. 10.1007/s100380050075
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- Publication type:
- Article
Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.
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- Nucleic Acids Research, 2007, v. 35, n. 4, p. 1198, doi. 10.1093/nar/gkm036
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- Publication type:
- Article
Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss.
- Published in:
- Molecular Human Reproduction, 2011, v. 17, n. 7, p. 447, doi. 10.1093/molehr/gar008
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- Publication type:
- Article
Frequent loss of heterozygosity at telomeric loci on 22q in sporadic colorectal cancers.
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- International Journal of Cancer, 1995, v. 60, n. 2, p. 174, doi. 10.1002/ijc.2910600207
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- Publication type:
- Article
Deletion mapping of the long arm of chromosome 22 in human meningiomas.
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- International Journal of Cancer, 1995, v. 60, n. 2, p. 178, doi. 10.1002/ijc.2910600208
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- Publication type:
- Article
Truncating variants of the sterol recognition region of SHH cause hypertelorism phenotype rather than hypotelorism‐holoprosencephaly.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 8, p. 1, doi. 10.1002/ajmg.a.63614
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- Publication type:
- Article
Two Japanese patients with Noonan syndrome‐like disorder with loose anagen hair 2.
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- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 7, p. 2246, doi. 10.1002/ajmg.a.62733
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- Publication type:
- Article
Lethal persistent pulmonary hypertension of the newborn in Bohring–Opitz syndrome.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 5, p. 1245, doi. 10.1002/ajmg.a.38681
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- Publication type:
- Article
A Novel PIGN Mutation and Prenatal Diagnosis of Inherited Glycosylphosphatidylinositol Deficiency.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 1, p. 183, doi. 10.1002/ajmg.a.37397
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- Publication type:
- Article
A Unique TBX5 Microdeletion with Microinsertion Detected in Patient with Holt-Oram Syndrome.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3192, doi. 10.1002/ajmg.a.37359
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- Publication type:
- Article
Genomic Organization of the Human Chondromodulin-1 Gene Containing a Promoter Region That Confers the Expression of Reporter Gene in Chondrogenic ATDC5 Cells.
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- Journal of Bone & Mineral Research, 2000, v. 15, n. 3, p. 421, doi. 10.1359/jbmr.2000.15.3.421
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- Publication type:
- Article
Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 139, doi. 10.1038/ng1001-139
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- Publication type:
- Article
A functional variation in the hypocretin neuropeptide precursor gene may be associated with obstructive sleep apnea syndrome in Japan.
- Published in:
- Laryngoscope, 2012, v. 122, n. 4, p. 925, doi. 10.1002/lary.23179
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- Publication type:
- Article
Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study.
- Published in:
- BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0681-y
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- Publication type:
- Article
An aggressive systemic mastocytosis preceded by ovarian dysgerminoma.
- Published in:
- 2020
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- Publication type:
- journal article
Mouse model for allogeneic immune reaction against fetus recapitulates human pre-eclampsia.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2008, v. 34, n. 1, p. 1, doi. 10.1111/j.1447-0756.2007.00679.x
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- Publication type:
- Article
Lack of association between orexin receptor gene polymorphisms and obstructive sleep apnea syndrome in Japanese.
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- Sleep & Biological Rhythms, 2011, v. 9, n. 2, p. 73, doi. 10.1111/j.1479-8425.2011.00487.x
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- Publication type:
- Article
Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient.
- Published in:
- Pediatric Pulmonology, 2014, v. 49, n. 3, p. E52, doi. 10.1002/ppul.22814
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- Publication type:
- Article
A case of early onset adenocarcinoma associated with colorectal polyposis with an unknown germline mutation.
- Published in:
- 2022
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- Publication type:
- Case Study
A case of early onset adenocarcinoma associated with colorectal polyposis with an unknown germline mutation.
- Published in:
- 2022
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- Publication type:
- Case Study
A Family with Craniofrontonasal Syndrome.
- Published in:
- Cleft Palate Craniofacial Journal, 2018, v. 55, n. 7, p. 1026, doi. 10.1597/15-347
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- Publication type:
- Article
Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0141739
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- Publication type:
- Article
Whole Genomic Analysis of an Unusual Human G6P[14] Rotavirus Strain Isolated from a Child with Diarrhea in Thailand: Evidence for Bovine-To-Human Interspecies Transmission and Reassortment Events.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0139381
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- Publication type:
- Article
Age-Related Decrease of Meiotic Cohesins in Human Oocytes.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0096710
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- Publication type:
- Article