ACHE Antibody (OASA09097)
- Known as:
- ACHE Antibody (OASA09097)
- Catalog number:
- oasa09097
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Aviva Systems Biology
- Gene target:
- ACHE Antibody (OASA09097)
Related genes to: ACHE Antibody (OASA09097)
- Gene:
- ACHE NIH gene
- Name:
- acetylcholinesterase (Cartwright blood group)
- Previous symbol:
- YT
- Synonyms:
- -
- Chromosome:
- 7q22.1
- Locus Type:
- gene with protein product
- Date approved:
- 1989-06-02
- Date modifiied:
- 2019-04-23
Related products to: ACHE Antibody (OASA09097)
Related articles to: ACHE Antibody (OASA09097)
- Preservation of articular cartilage remains the fundamental objective of hip-preservation surgery. Although acetabular labral pathology is commonly discussed in terms of pain, stability, and restoration of the suction seal, its influence on cartilage loading may be equally important. Increasing evidence suggests that disruption of labral integrity alters the mechanical environment of the hip by concentrating forces over smaller areas of articular cartilage, whereas restoration of the labrum can normalize load distribution toward native conditions. Although biomechanical improvements do not necessarily predict long-term clinical outcomes, they provide important insight into the mechanisms by which contemporary hip-preservation procedures may benefit patients. Ultimately, the value of labral repair may extend beyond treatment of a torn structure itself; the true goal may be protection of articular cartilage and preservation of long-term joint health. - Source: PubMed
Publication date: 2026/09/13
McCabe Michael P - Ulcerative colitis (UC) has a complex multifocal etiology that includes immune dysregulation of the gut microbiome leading to pro-inflammatory cytokine release. UC may present initially through subclinical manifestations such as sacroiliitis due to underlying inflammation, known as the gut-joint axis. JAK inhibition provides an effective treatment method for overlapping intestinal and articular inflammation. - Source: PubMed
Publication date: 2026/07/16
Hajijama SameeraSheikh Ibrahim AbdullatifJama Hawa AliShikh HamzaAli NagoudRafat A Samman AbdulrahmanAden Abdulahi MGil Melmed YAlbar Nezar Y - Cocoon syndrome, also known as sclerosing encapsulating peritonitis (SEP), is a rare condition characterized by the encapsulation of small bowel loops by a thick fibrocollagenous membrane. Its non-specific clinical presentation and ambiguous findings on conventional imaging often lead to significant diagnostic delays or misdiagnosis, frequently being mistaken for internal hernias or neoplastic processes. We present the case of a 61-year-old male patient with no prior abdominal surgical history who presented with a six-month history of recurrent abdominal pain, vomiting, and weight loss. While magnetic resonance imaging and computed tomography suggested a high-grade intestinal obstruction, they could not definitively rule out an underlying malignancy. Exploratory laparoscopy was performed, revealing a dense fibrin mantle encapsulating the small bowel loops and a carnified greater omentum. Extensive laparoscopic blunt and bipolar adhesiolysis was successfully carried out, achieving complete intestinal release. The patient experienced an excellent postoperative recovery and was discharged five days after the procedure. This case highlights the pivotal role of exploratory laparoscopy as a minimally invasive tool that provides both definitive diagnostic confirmation and effective surgical treatment, reducing the morbidity associated with traditional laparotomy in cases of ambiguous intestinal obstruction. - Source: PubMed
Publication date: 2026/08/13
Wosiack Menin Amanda IPadilla RicardoProaño GabrielaPinedo SofíaWosiack Luana - Small bowel lymphangiomatosis is a rare benign lymphatic malformation with nonspecific clinical manifestations that may complicate preoperative diagnosis. We present the case of a 57-year-old male with a history of recurrent umbilical hernias who complained of abdominal pain, nausea, vomiting, and an unreducible ventral hernia, all of which suggested a small bowel obstruction. Imaging revealed a presumed strangulated hernia with bowel obstruction and abnormal thickening of various loops of small bowel. Exploratory laparotomy disclosed incarcerated and gangrenous small bowel requiring resection. Histopathologic evaluation demonstrated extensive small-bowel lymphangiomatosis with concurrent AA-dominant amyloidosis, confirmed by apple-green birefringence on polarized microscopy of a Congo red-stained sample. This case highlights a rare coexistence of lymphangiomatosis and amyloidosis and suggests a possible relationship between chronic inflammatory amyloid deposition and secondary lymphatic obstruction, which may contribute to lymphangioma formation. - Source: PubMed
Publication date: 2026/08/13
Naljian Garo JPatel Rachna PMcqueary Tamaya SGrasso SalvatoreQiao Jian-Hua - Acute lymphoblastic leukemia (ALL) is the most common pediatric hematologic malignancy and is frequently associated with significant oral complications resulting from the disease as well as the treatment-related immunosuppression. In such conditions, odontogenic infections may progress rapidly and contribute to systemic morbidity, thereby necessitating proper and carefully coordinated dental management. A four-year-old boy diagnosed with ALL, in the maintenance phase of chemotherapy, presented with pain and swelling in the lower right back tooth region for five days. Clinical and radiographic examination revealed a dentoalveolar abscess associated with the right deciduous mandibular second molar, along with multiple carious lesions involving other teeth. Following consultation with the pediatric oncologist and assessment of hematological parameters, a comprehensive dental rehabilitation was performed under strict infection control measures. Treatment included a pulpectomy of the right deciduous mandibular second molar, followed by placement of a stainless-steel crown and restorative management of other carious lesions. The child demonstrated complete resolution of pain and swelling, preservation of the affected primary tooth, restoration of masticatory function, and significant improvement in oral health during the follow-up visits. No postoperative complications or interruption of ongoing chemotherapy occurred. This case highlights that conservative management of an infected primary molar can be considered and safely done in children with ALL if their medical condition and hematological status permit. Also, careful treatment planning and multidisciplinary coordination with the oncologist allowed elimination of the oral foci of infection while preserving the teeth and maintaining arch integrity. - Source: PubMed
Publication date: 2026/08/13
Sudarsanan AswathyBarretto Elaine SSwamy Dinesh FSanvordekar RuhiSajeev Devika