Biomedical publications with connected research

Paraquat exposure as an etiological factor of Parkinson's disease

2006-07-06 | PMID 16815551

siRNA targeted against HAb18G/CD147 inhibits MMP-2 secretion, actin and FAK expression in hepatocellular carcinoma cell line via ERK1/2 pathway

2006-07-06 | PMID 16815629

The BCL6 proto-oncogene: a leading role during germinal center development and lymphomagenesis

2006-07-06 | PMID 16815642

Transcriptional regulation of the human α2(I) collagen gene (COL1A2), an informative model system to study fibrotic diseases

2006-06-12 | PMID 16815696

Predictive value of in vitro safety studies

2006-07-06 | PMID 16815733

Human red blood cell polymorphisms and malaria

2006-07-06 | PMID 16815736

Genetics of obesity

2006-06-15 | PMID 16815794

The role of the central melanocortin system in the regulation of food intake and energy homeostasis: lessons from mouse models

2006-06-15 | PMID 16815803

Aberrant Wnt/β-catenin signaling can induce chromosomal instability in colon cancer

2006-07-01 | PMID 16815967

CTCF binding at the <i>H19</i> imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to <i>Igf2</i>

2006-07-01 | PMID 16815976

No associations of human pulmonary tuberculosis with Sp110 variants

2006-06-30 | PMID 16816019

CHEK2 I157T associates with familial and sporadic colorectal cancer

2006-06-30 | PMID 16816021

A novel susceptibility locus for Hirschsprung’s disease maps to 4q31.3–q32.3

2006-06-30 | PMID 16816022

Increased BACE1 maturation contributes to the pathogenesis of Alzheimer's disease in Down syndrome

2006-06-30 | PMID 16816111

BACE2, as a novel APP θ‐secretase, is not responsible for the pathogenesis of Alzheimer's disease in Down syndrome

2006-06-30 | PMID 16816112

Functional interaction of VEGF‐C and VEGF‐D with neuropilin receptors

2006-06-30 | PMID 16816121

Intracellular Protein Degradation: From a Vague Idea Thru the Lysosome and the Ubiquitin-Proteasome System and onto Human Diseases and Drug Targeting *

2006-07-01 | PMID 16816126

Physiology of Local Renin-Angiotensin Systems

2006-06-30 | PMID 16816138

The SloR/Dlg Metalloregulator ModulatesStreptococcus mutansVirulence Gene Expression

2006-06-30 | PMID 16816176

Large-scale gene expression studies of the endometrium: what have we learnt?

2006-07-01 | PMID 16816328

Microarray technology offers a novel tool for the diagnosis and identification of therapeutic targets for male infertility

2006-07-01 | PMID 16816329

The absence of a Ca2+ signal during mouse egg activation can affect parthenogenetic preimplantation development, gene expression patterns, and blastocyst quality

2006-07-01 | PMID 16816332

Quantification of healthy follicles in the neonatal and adult mouse ovary: evidence for maintenance of primordial follicle supply

2006-07-01 | PMID 16816336

Measles case imported from Europe to Victoria, Australia, March 2006.

Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin | 2006-05-18 | PMID 16816463

Riddell M A, Lynch P, Jin L and 1 more

Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene

2006-06-30 | PMID 16816952

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus

2006-06-30 | PMID 16816970

Improvement in serial cardiopulmonary exercise testing following enzyme replacement therapy in Fabry disease

2006-06-30 | PMID 16817011

Molecular epidemiology of African swine fever virus studied by analysis of four variable genome regions

2006-07-01 | PMID 16817033

Mutational analysis of the follistatin-related gene in women with premature ovarian failure and polycystic ovary syndrome.

Acta obstetricia et gynecologica Scandinavica | 2006-01-01 | PMID 16817091

Kimura Fuminori, Takebayashi Koichi, Fujiwara Mutsuko and 3 more

[Focal segmental glomerulosclerosis (FSGS). Molecular defects and clinical relevance].

Deutsche medizinische Wochenschrift (1946) | 2006-07-07 | PMID 16817104

Schiffer M, Haller H

[Familial hyperparathyroidism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817340

Suzuki Shinichi

[Neonatal hyperparathyroidism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817341

Nakagawa Yuichi

[Hyperparathyroidism--jaw tumor syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817342

Mizuki Kazuhito, Okabe Taijiro, Yanase Toshihiko

[Idiopathic hypoparathyroidism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817345

Yamamoto Michiko

[Familial isolated hypoparathyroidism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817346

Takeuchi Yasuhiro

[Pseudohypoparathyroidism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817350

Yasuda Toshiyuki

[Albright hereditary osteodystrophy].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817351

Kitaoka Taichi, Ozono Keiichi

[Pseudoidiopathic hypoparathyroidism and pseudopseudohypoparathyroidism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817352

Okazaki Ryo

[Hypophosphatasia].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817361

Inoue Masaru

[Dent's disease].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817362

Igarashi Takashi

[Vitamin D-dependent rickets type I, II].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817363

Fujiwara Ikuma

[Osteogenesis imperfecta].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817368

Ito Hironori, Yazaki Susumu, Takamine Yuji and 1 more

[Paget disease of bone].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817369

Okada Kyoji, Takahashi Shu, Nagasawa Hiroyuki and 1 more

[Familial and sporadic hypocalciuric hypercalcemia].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817377

Yamauchi Mika, Sugimoto Toshitsugu

[Congenital hypogonadotropic hypogonadism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817387

Ujihara Makoto

[Kallmann syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817388

Sato Naoko, Ogata Tsutomu

[Ovarian insufficiency (so called 'poor responder')].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817421

Ohba Takashi, Okamura Yoshinori, Okamura Hitoshi

[Familial breast cancer, ovarian cancer].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817423

Inoue Masaki

[Denys-Drash syndrome (DDS)].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817450

Sasaki Nozomu

[Frasier syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817451

Kohsaka Takao, Tagawa Manabu, Koinuma Sachi and 1 more

[Noonan syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817452

Ogata Tsutomu

[True hermaphroditism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817453

Shiraishi Koji, Naito Katsusuke

[XY female].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817454

Tsutsumi Osamu

[Leydig cell hypoplasia (Leydig cell aplasia)].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817462

Arisaka Osamu, Koyama Satomi

[Hermaphroditism].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817465

Shima Hiroki, Yamamoto Shingo

[17alpha-hydroxylase/17,20lyase deficiency].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817466

Noguchi Kazumi

[17beta-hydroxysteroid dehydrogenase deficiency].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817467

Ohzeki Takehiko, Nakagawa Yuichi

[Testicular feminization].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817470

Ida Shinobu, Shimada Kenji

[Steroid 5alpha-reductase deficiency].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817471

Tohda Akira

[Cryptorchidism and chromosomal anomalies (Edwards, Patau, Lowe syndrome)].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817473

Kawamura Hideki, Hirai Kotaro, Usuda Kazumasa and 1 more

[Testotoxicosis].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817479

Fuse Hideki, Akashi Takuya, Watanabe Akihiko

[Adrenogenital syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817483

Fujieda Kenji

[Hand-foot-genital syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817484

Mitsubuchi Hiroshi, Endo Fumio

[Rokitansky syndrome].

Nihon rinsho. Japanese journal of clinical medicine | 2006-06-28 | PMID 16817485

Tsutsumi Osamu

THE EVOLUTION OF PARASITES IN RESPONSE TO TOLERANCE IN THEIR HOSTS: THE GOOD, THE BAD, AND APPARENT COMMENSALISM

2006-05-01 | PMID 16817535

Comparative analysis and integrative classification of NCI60 cell lines and primary tumors using gene expression profiling data

2006-07-03 | PMID 16817967

The predominance of Human Immunodeficiency Virus type 1 (HIV-1) circulating recombinant form 02 (CRF02_AG) in West Central Africa may be related to its replicative fitness

2006-07-03 | PMID 16817969

Molecular signatures (unique proteins and conserved indels) that are specific for the epsilon proteobacteria (Campylobacterales)

2006-07-04 | PMID 16817973

The Diverse Clinical Manifestations of Tuberous Sclerosis Complex: A Review

2006-03-01 | PMID 16818173

The Neurobiology of Tuberous Sclerosis Complex

2006-03-01 | PMID 16818174

Genetic Aspects of Neurocutaneous Disorders

2006-03-01 | PMID 16818175

From Plasmids to Protection: A Review of DNA Vaccines Against Infectious Diseases

2006-01-01 | PMID 16818367

Purkinje cell death: Differences between developmental cell death and neurodegenerative death in mutant mice

2006-06-01 | PMID 16818391

Von Hippel–Lindau Disease: Molecular Pathological Basis, Clinical Criteria, Genetic Testing, Clinical Features of Tumors and Treatment

2006-06-01 | PMID 16818478

Pharmacogenetics of anticancer drug sensitivity in pancreatic cancer

2006-06-01 | PMID 16818496

Roles of nonhomologous end-joining pathways in surviving topoisomerase II–mediated DNA damage

2006-06-01 | PMID 16818498

Genotoxic-activated G2-M checkpoint exit is dependent on CDC25B phosphatase expression

2006-06-01 | PMID 16818502

Red-Hed regulation: recombinase Rad51, though capable of playing the leading role, may be relegated to supporting Dmc1 in budding yeast meiosis.

Genes & development | 2006-07-01 | PMID 16818601

Sheridan Sean, Bishop Douglas K

Non–Small-Cell Lung Cancer and Ba/F3 Transformed Cells Harboring the ERBB2 G776insV_G/C Mutation Are Sensitive to the Dual-Specific Epidermal Growth Factor Receptor and ERBB2 Inhibitor HKI-272

2006-07-01 | PMID 16818618

Conditional Activation of RET/PTC3 and BRAFV600E in Thyroid Cells Is Associated with Gene Expression Profiles that Predict a Preferential Role of BRAF in Extracellular Matrix Remodeling

2006-07-01 | PMID 16818623

MYC Can Induce DNA Breaks In vivo and In vitro Independent of Reactive Oxygen Species

2006-07-01 | PMID 16818632

Δ9-Tetrahydrocannabinol Inhibits Cell Cycle Progression in Human Breast Cancer Cells through Cdc2 Regulation

2006-07-01 | PMID 16818634

NUP98-HOXA9 Induces Long-term Proliferation and Blocks Differentiation of Primary Human CD34+ Hematopoietic Cells

2006-07-01 | PMID 16818636

Pim-3, a Proto-Oncogene with Serine/Threonine Kinase Activity, Is Aberrantly Expressed in Human Pancreatic Cancer and Phosphorylates Bad to Block Bad-Mediated Apoptosis in Human Pancreatic Cancer Cell Lines

2006-07-01 | PMID 16818649

HDJ-2 as a Target for Radiosensitization of Glioblastoma Multiforme Cells by the Farnesyltransferase Inhibitor R115777 and the Role of the p53/p21 Pathway

2006-07-01 | PMID 16818651

Metastasis Suppressor Proteins: Discovery, Molecular Mechanisms, and Clinical Application

2006-07-01 | PMID 16818682

<i>MECT1-MAML2</i> Fusion Transcript Defines a Favorable Subset of Mucoepidermoid Carcinoma

2006-07-01 | PMID 16818685

Molecular Profiling of Laser-Microdissected Matched Tumor and Normal Breast Tissue Identifies Karyopherin α2 as a Potential Novel Prognostic Marker in Breast Cancer

2006-07-01 | PMID 16818692

A Distinct p53 Protein Isoform Signature Reflects the Onset of Induction Chemotherapy for Acute Myeloid Leukemia

2006-07-01 | PMID 16818696

Complement-Induced Cell Death by Rituximab Depends on CD20 Expression Level and Acts Complementary to Antibody-Dependent Cellular Cytotoxicity

2006-07-01 | PMID 16818702

Cutting Edge: Human β Defensin 3—A Novel Antagonist of the HIV-1 Coreceptor CXCR4

2006-07-01 | PMID 16818731

Roles of the Ig κ Light Chain Intronic and 3′ Enhancers in Igk Somatic Hypermutation

2006-07-01 | PMID 16818772

Streptococcal M Protein: A Multipotent and Powerful Inducer of Inflammation

2006-07-01 | PMID 16818781

A primary candidate gene for obsessive-compulsive disorder.

Archives of general psychiatry | 2006-07-01 | PMID 16818860

Leckman James F, Kim Young-Shin

Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of Drosophila Pink1 is rescued by Parkin

2006-07-05 | PMID 16818890

Evidence of a new human genotype susceptible to variant CJD.

Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin | 2006-06-01 | PMID 16819115

Ward H J T

Adrenal Myelolipomas Show Nonrandom X-chromosome Inactivation in Hematopoietic Elements and Fat: Support for a Clonal Origin of Myelolipomas

2006-06-22 | PMID 16819325

Inflammation and the Host Response to Injury: An Overview of the Multicenter Study of the Genomic and Proteomic Response to Burn Injury

2006-07-01 | PMID 16819346

Impact of Pretransplant Growth Retardation in Pediatric Liver Transplantation

2006-07-01 | PMID 16819383

Allogeneic bone marrow transplantation for hypereosinophilic syndrome: long-term follow-up with eradication of FIP1L1-PDGFRA fusion transcript

2006-07-03 | PMID 16819435